Abstract
Multifactorial causes can lead to osteoarthritis (OA), and its pathogenesis is not clearly understood as yet. The main characteristics of OA are the slowly progressing deterioration of the articular cartilage, accompanied by intermitted painful inflammatory episodes, and a continuous subchondral bone remodeling, often resulting in osteophyte formation in nonweight-bearing joint areas. Because of the lack of innervation and vascularization of cartilage, the destruction of this specific tissue remains unnoticed until other joint compartments are involved such as synovial membranes, answering with reactive synovitis to cartilage debris, or mechanoreception changes in the underlying bone, or until the diminution of articular cartilage results in a radiographically detectable joint space narrowing.
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References
Akatsuka M, Yamamoto Y, Tobetto K, Yasui T, Ando T (1993) In vitro effects of hyalurononan on prostaglandin E2 induction by interleukin-I in rabbit articular chondrocytes. Agents Actions 38: 122–125
Bulstra SK, Kuijer R, Buurman WA, Terwindt-Rouwenhorst E, Guelen PJM, van der Linden AJ (1992) The effect of piroxicam on the metabolism of isolated human chondrocytes. Clin Orthop 277: 289–296
Collier S, Ghosh P (1991) Comparison of the effects of non-steroidal anti-inflammatory drugs ( NSAIDs) on proteoglycan synthesis by articular cartilage explant and chondrocyte monolayer cultures. Biochem Pharmacol 41: 1375–1384
Green GD, Chipman SD, Birkhead JR, Troubetskoy OV, Goldring MB (1995) Interleukin-1 modulation of matrix metalloprotease and proteoglycan expression in human chondrocytes immortalized by simian virus 40. Trans Orthop Res Soc 20: 334
Ismaiel S, Hollander AP, Atkins RM, Elson CJ (1991) Differential responses of human and rat cartilage to degrading stimuli in-vitro. J Pharm Pharmacol 43: 207–209
Korver GHV, van de Stadt RJ, van Kampen GPJ, Kiljan E, van der Korst JK (1989) Bovine sesamoid bones: a culture system for anatomically intact articular cartilage. In Vitro Cell Dev Biol 25: 1099–1106
Mohamed-Ali H (1992) Influence of synovial cells on cartilage in vitro: induction of breakdown and inhibition of synthesis. Virchows Archiv B Cell Pathol 62: 227–236
Seed MP, Ismaiel S, Cheung CY, Thomson TA, Gardner CR, Atkins RM, Elson CJ (1993) Inhibition of interleukin lß induced rat and human cartilage degradation in vitro by the metalloproteinase inhibitor U27391. Ann Rheum Dis 52: 37–43
Seong SC, Matsumura T, Lee FY, Whelan MC, Li XQ, Trippel SB (1994) Insulin-like growth factor I regulation of swarm rat chondrosarcoma chondrocytes in culture. Exp Cell Res 211: 238–244
Shimazu A, Jikko A, Iwamoto M et. al (1993) Effects of hyaluronic acid on the release of proteoglycan from the cell matrix in rabbit chondrocyte cultures in the presence and absence of cytokines. Arthr Rheum 36: 247–253
Srinivas GR, Chichester CO, Barrach HJ, Matoney AL (1994) Effects of certain antiarthritic agents on the synthesis of type Il collagen and glycosaminoglycans in rat chondrosarcoma cultures. Agents Actions 41: 193–199
Venn G, Lauder RM, Hardingham TE, Muir H (1990) Effects of catabolic and anabolic cytokines on proteoglycan biosynthesis in young, old and osteoarthritic canine cartilage. Biochem Soc Trans 18: 973–974
Verschure PJ, van der Kraan PM, Vitters EL, van den Berg WB (1994) Stimulation of proteoglycan synthesis by triamcinolone acetonide and insulin-like growth factor 1 in normal and arthritic murine articular cartilage. J Rheumatol 21: 920–926
Vignon E, Mathieu P, Louisot P, Richard M (1991) In vitro effect of nonsteroidal antiinflammatory drugs on proteoglycanase and collagenase activity in human osteoarthritic cartilage. Arthr Rheum 34: 1332–1335
Yu LP, Jr, Smith GN, Jr, Hasty KA, Brandt KD (1991) Doxycycline inhibits type XI collagenolytic activity of extracts from human osteoarthritic cartilage and of gelatinase. J Rheumatol 18: 1450–1452
Zafarullah M, Martel-Pelletier J, Cloutier JM, Gedamu L, Pelletier JP (1992) Expression of c-fos, c-jun, jun-B, metallothionein and metalloproteinase genes in human chondrocyte. FEBS 306: 169–172
Archer CW, McDowell J, Bayliss MT, Stephens MD, Bentley G (1990) Phenotypic modulation in sub-populations of human articular chondrocytes in vitro. J Cell Sci 97: 361–371
Aydelotte MB, Greenhill RR, Kuettner KE (1988) Differences between sub-populations of cultured bovine articular chondrocytes. II. Proteoglycan metabolism. Conn Tiss Res 18: 223–234
Aydelotte MB, Kuettner KE (1988) Differences between sub-populations of cultured bovine articular chondrocytes. I. Morphology and cartilage matrix production. Conn Tiss Res 18: 205–222
Aydelotte MB, Raiss RX, Caterson B, Kuettner KE (1992) Influence of interleukin-1 on the morphology and proteoglycan metabolism of cultured bovine articular chondrocytes. Conn Tiss Res 28: 143–159
Bassleer C, Henrotin Y, Franchimont P (1990) In vitro assays of chondrocyte functions: the influence of drugs and hormones. Scand J Rheumatology (Suppl 81 ): 13–20
Bassleer CT, Henrotin YE, Reginster JYL, Franchimont PP (1992) Effects of tiaprofenic acid and acetylsalicylic acid on human articular chondrocytes in 3-dimensional culture. J Rheumatol 19: 1433–1438
Benya PD, Schaffer JD (1982) Dedifferentiated chondrocytes reexpress the differentiated collagen phenotype when cultured in agarose gels. Cell 30: 215–224
Bonaventure J, Kadhom N, Cohen-Solal L, Ng KH, Bourguignon J, Lasselin C, Freisinger P (1994) Reexpression of cartilage-specific genes by dedifferentiated human articular chondrocytes cultured in alginate beads. Exp Cell Res 212: 97–104
Guo J, Jourdian GW, MacCallum DK (1989) Culture and growth characteristics of chondrocytes encapsulated in alginate beads. Conn Tiss Res 19: 277–297
Häuselmann HJ, Fernandes RJ, Mok SS, Schmid TM, Block JA, Aydelotte MB, Kuettner KE, Thonar EJMA (1994) Phenotypic stability of bovine articular chondrocytes after long-term culture in alginate beads. J Cell Sci 107: 17–27
Henrotin Y, Bassleer C, Franchimont P(1992) In vitro effects of etodolac and acetylsalicylic acid on human chondrocyte metabolism. Agents Actions 36:317–323
Jortikka M, Lammi MJ, Parkkinen JJ, Lahtinen R, Tammi MI (1993) A high sensitivity dot-blot assay for proteoglycans by cuprolinic blue precipitation. Conn Tiss Res 29: 263–272
Kolibas LM, Goldberg RL (1989) Effect of cytokines and anti-arthritic drugs on glycosaminoglycan synthesis by bovine articular chondrocytes. Agents Actions 27: 245–249
Lane NE, Williams III RJ, Schurman DJ, Smith RL (1992) Inhibition of interleukin 1 induced chondrocyte protease activity by a corticosteroid and a nonsteroidal antiinflammatory drug. J Rheumatol 19: 135–139
Malemud CJ, Stevenson S, Mehraban F, Papay RS, Purchio AF, Goldberg VM (1994) The proteoglycan synthesis repertoire of rabbit chondrocytes maintained in type II collagen gels. Osteoarthritis and Cartilage 2: 29–42
McCollum R, Martel-Pelletier J, DiBattista J, Pelletier JP (1991) Regulation of interleukin 1 receptors in human articular chondrocytes. J Rheumatol (Suppl 27 ) 18: 85–88
Seid JM, Rahman S, Graveley R, Bunning RAD, Nordmann R, Wishart W, Russel RG (1993) the effect of interleukin-1 on cytokine gene expression in cultured human articular chondrocytes analyzed by messenger RNA phenotyping. Arthritis and Rheumatism 36: 35–43
van der Kraan P, Vitters E, van den Berg W (1992) Differential effect of transforming growth factor ß on freshly isolated and cultured articular chondrocytes. J Rheumatol 19: 140–145
Verbruggen G, Veys EM, Wieme N, Malfait AM, Gijselbrecht L, Nimmegeers J, Almquist KF, Broddelez C (1990) The synthesis and immobilisation of cartilage-specific proteoglycan by human chondrocytes in different concentrations of agarose. Clin Exp Rheumatol 8: 371–378
Aydelotte MB, Schleyerbach R, Zeck BJ, Kuettner KE (1986) Articular chondrocytes cultured in agarose gel for study of chondrocytic chondrolysis. In: Kuettner (ed) Articular Cartilage Biochemistry. Raven Press, New York, pp 235–256
Oestensen M, Veiby OP, Raiss R, Hagen A, Pahle J (1991) Responses of normal and rheumatic human articular chondrocytes cultured under various experimental conditions in agarose. Scand J Rheumatol 20: 172–182.
Raiss RX, Karbowski A, Aigner T, Schleyerbach R (1995) Chondrocytes and antirheumatic drugs. J Rheumatol (Suppl 43 ) 22: 152–154
Raiss RX, Oestensen M, Aydelotte MB (1992) Drug evaluation on isolated articular chondrocytes. In: Kuettner K et al, eds. Articular Cartilage and Osteoarthritis, Raven Press Ltd, New York pp. 569–582
Verbruggen G, Veys EM, Malfait AM, Schatteman L, Wieme N, Heynen G, Vanhoutte V, Broddelez C (1989) Proteoglycan metabolism in isolated chondrocytes from human cartilage and in short-term tissue-cultured human articular cartilage. Clin Exp Rheumatol 7: 13–17
Chayen J, Bitensky L, Mehdizadeh S, Dunham J, Older J (1994) Testing drugs on human osteoarthritic articular cartilage. Cell Biochem Funct 12: 63–68
Lafeber FPG, van Roy H, Wilbrink B, Huber-Bruning O, Bijlsma JWJ (1992) Human osteoarthritic cartilage is synthetically more active but in culture less vital than normal cartilage. J Rheumatol 19: 123–129
Lafeber FPJG, van der Kraan PM, van Roy JLAM, Huber-Bruning O, Bijlsma JWJ (1993) Articular cartilage explant culture; an appropriate in vitro system to compare osteoarthritic and normal human cartilage. Conn Tiss Res 29: 287–299
McQuillan DJ, Handley CJ, Robinson HC (1986) Control of proteoglycan biosynthesis. Biochem J 237: 741–747
Nixon JS, Bottomley KMK, Broadhust MJ et. al (1991) Potent collagenase inhibitors prevent interleukin-1-induced cartilage degradation in vitro. Int J Tiss Reac 13: 237–243
Pelletier JP, Cloutier JM, Martel-Pelletier J (1989) In vitro effects of tiaprofenic acid, sodium salicylate and hydrocortisone on the proteoglycan metabolism of human osteoarthritic cartilage. J Rheumatol 16: 646–655
Pelletier JP, Martel-Pelletier J (1989) Evidence for the involvement of interleukin 1 in human osteoarthritic cartilage degradation: protective effect of NSAID. J Rheumatol (Suppl 18 ) 16: 19–27
Verbruggen G, Veys EM, Malfait AM et. al (1989) Proteoglycan metabolism in tissue cultured human articular cartilage. Influence of piroxicam. J Rheumatol 16: 355–362
Verbruggen G, Veys EM, Malfait AM et. al (1990) Proteoglycan metabolism in tissue-cultured human articular cartilage. Scand J Rheumatology 19: 257–268
Yang XH, Zhang ZX (1991) Effects of DMSO and glycerol in 35S incorporation of articular cartilage. Cryo-Letters 12: 53–58
Adams ME, Billingham MFJ (1982) Animal models of degenerative joint disease. Current Topics in Pathology 71: 265–297
Bendele AM, Hulman JF (1988) Spontaneous cartilage degeneration in guinea pigs. Arthr Rheum 31: 561–565
Burton-Wurster N, Todhunter RJ, Lust G (1993) Animal models of osteoarthritis. In. Woessner JF, Howell DS (eds.) Joint cartilage degradation. Basic and clinical aspects. New York, Marcel Dekker Inc.: 347–384
Carney SL (1991) Cartilage research, biochemical, histologic, and immunohistochemical markers in cartilage, and animal models of osteoarthritis. Current Opinion Rheumatol 3: 669–675
Colombo C, Butler M, O’Byrne E, Hickman L (1983) A new model of osteoarthritis in rabbits. I: Development of knee joint pathology following lateral meniscectomy and section of the fibular collateral and sesamoid ligaments. Arthr Rheum 26: 875–886
Farkas T, Boyd RD, Schaffler MB, Radin EL, Burr DB (1987) Early vascular changes in rabbit subchondral bone after repetitive impulsive loading. Clin Orthop 30: 259–267
Greenwald RA (1991) Animal models for evaluation of arthritis drugs. Meth Find Clin Pharmacol 13: 75–83
Greenwald RA (1993) Cartilage degradation in animal models of inflammatory joint disease. In: Woessner JF, Howell DS (eds.) Joint cartilage degradation. Basic and clinical aspects. New York, Marcel Dekker Inc.: 385–408
Greenwald RA, Diamond HS eds (1988) CRC Handbook of animal models for the rheumatic diseases CRC press Boca Raton Vol 1
Haakenstad LH (1969) Chronic bone and joint diseases in relation to conformation in the horse. Eq Vet J 1: 248
Hess EV, Herman JH (1986) Cartilage metabolism and anti- inflammatory drugs in osteoarthritis. Am J Med 81: 36–43
Kalbhen DA (1983) Pharmakologische Beurteilung von Möglichkeiten einer Knorpelschutztherapie bei degenerativen Gelenkerkrankungen (Arthrose). Z Rheumatol 42: 187–194
Kalbhen DA (1987) Chemical model of osteoarthritis — a pharmacological evaluation. J Rheumatol 14: 130–131
Lindenhayn K, Haupt R, Kristan J, Regling G (1984) Proteinase activity in the joint cartilage of sheep following mechanical arthrosis induction using an impulse stress instrument. Beitr Orthop Traumatol 31: 507–511
Lust G, Rendano VT, Summers BA (1985) Canine hip dysplasia: concepts and diagnosis. J Am Vet Med Assoc 187: 638–640
Malemud CJ (1993) Markers of osteoarthritis and cartilage research in animal models. Current Opinion in Rheumatology 5: 494–502
Mazières B, Herou P, Dambreville JM, Thiechart H (1984) Die Wirkung eines Glykosaminoglykan-Peptid-Komplexes ( GAG-Peptid-Komplex) bei experimenteller Arthrose am Kaninchen. Akt Rheumatol 9: 133–138
Meacock SCR, Bodmer JL, Billingham MFJ (1990) Experimental osteoarthritis in guinea pigs. J Exp Pathol 71: 279–293
Meyer-Carrive I, Ghosh P (1992) Effects of tiaprofenic acid ( Surgam) on cartilage proteoglycans in the rabbit joint immobilization model. Ann Rheum Dis 51: 448–455
Moskowitz RW (1990) The relevance of animal models in osteoarthritis. Scand J Rheum 81 (Suppl): 21–23
Moskowitz RW (1992) Experimental models of osteoarthritis. In: Moskowitz RW, Howell DS, Goldberg VM, Mankin HJ (eds.) Osteoarthritis: Diagnosis and medical/surgical management. 2nd ed. Philadelphia: W.B.Saunders. pp 213–232
Moskowitz RW, Davis W, Sammarco J, Martens M, Baker J, Mayor M, Burstein AH, Frankel BH (1973) Experimentally induced degenerative joint lesions following partial menisectomy in the rabbit. Arthr Rheum 16: 397–405
Moskowitz RW, Howell DS, Goldberg VM, Muniz O, Pita JC (1979) Cartilage proteoglycan alterations in an experimentally induced model of rabbit osteoarthritis. Arthr Rheum 22: 155–163
Palmoski MJ, Brandt KD (1982) Aspirin aggravates the degeneration of canine joint cartilage caused by immobilization. Arthritis Rheum 25: 1333–1342
Pita JC, Manicourt DH, Muller FJ, Howell DS (1986) Studies on the potential reversibility of osteoarthritis in some experimental animal models. In Kuettner KE, Schleyerbach R, Hascall VC eds Articular cartilage biochemistry. Raven Press New York, 349–363
Pritzker KPH (1994) Animal models for Osteoarthritis: Processes, problems, and prospects. Ann Rheum Dis 53: 406–420
Pritzker KPH, Chateauvert JM, Grynpas MD, Renlund RC, Turnquist J, Kessler MJ (1989) Rhesus macaques as an experimental model for degenerative arthritis. P R Health Sci J 8: 99–102
Schwartz ER (1985) Surgically induced osteoarthritis in guinea pigs: studies of proteoglycans, collagens, and non-collagen proteins. In: Peyron JG, ed. Osteoarthritis: current clinical and fundamental problems. Proc of a Workshop held in Paris April 9–11, 1984. Rueil-Malmaison: Geigy: 273–288
Todhunter RJ, Lust G (1992) Synovial joint anatomy, biology and pathobiology. In: Auer J, ed. Equine Surgery Philadelphia, Saunders:844–866
Williams JM, Uebelhart D, Ongchi DR, Kuettner KE, Thonar EJMA (1992) Animal models of articular cartilage repair. In: Kuettner KE, Schleyerbach R, Pyron JG, Hascall VC (eds.) Articular cartilage and osteoarthritis. New York Raven Press:511–525
Abatangelo G, Botti P, Del Bue M, Gei G, Samson JC, Cortivo R, DeGalateo A, Martelli M (1989) Intra-articular sodium hyaluronate injections in the Pond-Nuki experimental model of osteoarthritis in dogs. I. Biochemical results. Clin Orthop Rel Res 241: 278–285
Adams ME, Pelletier JP (1988) Canine anterior cruciate ligament transection model of osteoarthritis. In Greenwald RA, Diamond HS (eds) CRC handbook of animal models for the rheumatic diseases CRC press Boca Raton Vol 2: 57–81
Brandt KD, Adams ME (1989) Exuberant repair of articular cartilage damage. Effect of anterior cruciate ligament transection in the dog. Trans Orthop Res Soc 14: 584
Brandt KD, Braunstein EM, Visco DM, O’Connor B. Heck D, Albrecht M (1991) Anterior (cranial) cruciate ligament transection in the dog: A bona fide model of osteoarthritis, not merely of cartilage injury and repair. J Rheumatol 18: 436–446
Brandt KD, Myers SL, Burr D, Albrecht M (1991) Osteoarthritic changes in canine articular cartilage, subchondral bone and synovium 54 months after transection of the anterior cruciate ligament. Arthr Rheum 34: 1560–1570
Colombo C (1988) Partial lateral meniscectomy with section of fibular collateral and sesamoid ligaments in the rabbit. In Greenwald RA, Diamond HS (eds) CRC handbook of animal models for the rheumatic diseases CRC press Boca Raton Vol 2: 27–55
DiPasquale G, Caputo CB, Crisman JW (1988) Rabbit partial medial meniscectomy. In Greenwald RA, Diamond HS (eds) CRC handbook of animal models for the rheumatic diseases CRC press Boca Raton Vol 2: 19–25
Hannan H, Ghosh P, Bellenger C, Taylor T (1987) Systemic administration of glycosaminoglycan polysulfate (arteparon) provides partial protection of articular cartilage from damage produced by meniscectomy in the canine. J Orthop Res 5: 47–59
Johnson RG (1986) Transection of the canine anterior cruciate ligament: a concise review of experience with this model of degenerative joint disease. Exp Pathol 30: 209–213
McDevitt C, Gilbertson E, Muir H (1977) An experimental model of osteoarthritis; early morphological and biochemical changes. J Bone Joint Surg 59B: 24–35
Myers SL, Brandt KD, O’Connor BL (1991) Low dose prednisone treatment does not reduce the severity of osteoarthritis in dogs after cruciate ligament transection. J Rheum 18: 1856–1862
Newton CII, Fetter DA, Bashey RI, Jimenez SA (1984) Clinical studies and pathological changes in articular cartilage in experimental canine osteoarthrosis and effects of the in vivo administration of a glycosaminoglycan peptide ( GAGPeptide-complex) from bone marrow and cartilage. Akt Rheumatol 9: 128–132
Pelletier JP, Martel-Pelletier J (1985) Cartilage degradation by neutral proteoglycanases in experimental osteoarthritis: suppression by steroids. Arthr Rheum 28: 1393
Pelletier JP, Martel-Pelletier J (1991) In vivo protective effects of prophylactic treatment with tiaprofenic acid or intraarticular corticosteroids on osteoarthritic lesions in the experimental dog model. J Rheumatol 18 (Suppl 27): 127–130
Pond MJ, Nuki G (1973) Experimentally-induced osteoarthritis in the dog. Ann Rheum Dis 32: 387
Schiavinato A, Lini E, Guidolin D, Pezzoli G, Botti P, Martelli M, Cortivo R, DeGalateo A, Abatangelo G (1989) Intraarticular sodium hyaluronate injections in the Pond-Nuki experimental model of osteoarthritis in dogs. II. Morphological findings. Clin Orthop Rel Res 241: 286–299
Schwartz E (1988) Surgically induced osteoarthritis in guinea pigs. In Greenwald RA, Diamond HS (eds) CRC handbook of animal models for the rheumatic diseases CRC press Boca Raton Vol 2: 89–95
Vignon E, Arlot M, Hartman D, Moyer B, Ville G (1983) Hypertrophic repair of articular cartilage in experimental osteoarthrosis. Ann Rheum Dis 42: 82–88
Chandrasekhar S, Esterman MA, Hoffman HA (1987) Microdetermination of proteoglycans and glycosaminoglycans in the presence of guanidine hydrochloride. Anal Biochem 161: 103–108
Farndale RW, Buttle DJ, Barrett AJ (1986) Improved quantitation and discrimination of sulphated glycosaminoglycans by use of dimethyl-methylene blue. Biochim Biophys Acta 883: 173–177
Karbowski A, Raiss RX, Schneider EJ (in prep) Continuous intraarticular therapy using an osmotic minipump Mankin Hi, Dorfman H, Lipiello L (1971) Biochemical and metabolic abnormalities in articular cartilage from osteoarthritic human hips. J Bone Joint Surgery 53A: 523–537
Romeis B (1989) Mikroskopische Technik. 17th ed Urban Schwarzenberg München
Rosenberg L (1971) Chemical basis for the histological use of safranin-O in the study of articular cartilage. J Bone Joint Surgery 53A: 69–82
vanderSluijs JA (1992) The reliability of the Mankin score for osteoarthritis. J Orthop Res 10: 58–61
Williams JM, Downey C, Thonar EJMA (1988) Increase in levels of serum keratan sulfate following cartilage proteoglycan degradation in the rabbit knee joint. Arthr Rheum 31: 557–560
Williams JM, Ongchi DR, Thonar EJMA (1993) Repair of articular cartilage injury following intra-articular chymopapain-induced matrix proteoglycan loss. J Orthop Res 11: 705–716
Benjamin M, Ralphs JR, Archer CW, Mason RM, Chambers M, Dowthwaite GP (1995) Cytoskeletal changes in articular fibrocartilage are an early indicator of osteoarthritis in STR/ORT mice. Orthop Res Soc 20: 246
Dunham J, Chambers MG, Jasani MK, Bitenski L, Chayen J (1989) Quantitative criteria for evaluating the early development of osteoarthritis and the effect of diclofenac sodium. Agents Actions 28: 93–97
Nakamura Y (1990) Histochemical and immunohistochemical studies on knee joint cartilage in spontaneous osteoarthritis in C57 black mice. J Tokyo Med Coll 48: 308–319
Pataki A, Graf HP, Witzemann E (1990) Spontaneous osteoarthritis of the knee-joint in C57BL mice receiving chronic oral treatment with NSAID’s or prednisone. Agents Actions 29: 210–217
Raiss RX, Bartlett RR, Schleyerbach R (1992) Genetically Induced Mouse Models of Rheumatic Diseases. Effects of Leflunomide on Articular Manifestations. In: Kuettner KE, Schleyerbach R, Pyron JG, Hascall VC (eds.) Articular cartilage and osteoarthritis. New York Raven Press: 712–713
Raiss RX, Caterson B (1992) Immunohistochemical localization of chondroitin sulfate isomers in the knee joint of osteoarthritic mice. In: Kuettner KE, Schleyerbach R, Pyron JG, Hascall VC (eds.) Articular cartilage and osteoarthritis. New York Raven Press:714–715
Schünke M, Tillmann B, Brück M, Müller-Ruchholtz W (1988) Morphologic characteristics of developing osteoarthrotic lesions in the knee cartilage of STR/1N mice. Arthr Rheum 31: 898–905
Sokoloff L, Crittenden LB, Yamamoto RS, Jay GE (1962) The genetics of degenerative joint disease in mice. Arthr Rheum 5: 531–545
Walton M (1977) Degenerative joint disease in the mouse knee; histological observations. J Pathol 123: 109–122
Walton M (1977) Degenerative joint disease in the mouse knee; radiological and morphological observations. J Pathol 123: 97–107
Walton M (1979) Patella displacement and osteoarthrosis of the knee joint in mice. J Pathol 127: 165–172
Walton M (1977) Studies of degenerative joint disease in the mouse knee joint; scanning electron microscopy. J Pathol 123: 211–217
Wilhelmi G, Maier R (1983) Zur Prüfung potentieller Antiarthrotika an der spontanen Arthrose der Maus. Z Rheumatol 42: 203–205
Bartlett RR, Dimitrijevic M, Mattar T, Zielinski T, Germann T, Rude E, Thoenes G H, Küchle CCA, Schorlemmer HU, Bremer E, Finnegan A, Schleyerbach R (1991). Leflunomide (HWA 486), a novel immunomodulating compound for the treatment of auto-immune disorders and reactions leading to transplantation rejection. Agents and Actions 32: 11–21
Broide D, Marquardt D, Wasserman S (1986) Effect of nedocromil sodium and sodium cromoglycate on connective tissue and bone marrow derived mast cells: acute and chronic studies. Eur J Respir Dis 69: (Suppl 147): 196–198
Church MK, Young KD (1983) The characteristics of inhibition of histamine release from human lung fragments by sodium cromoglycate, salbutamol and chlorpromazine. Br J Pharmacol 78: 671–679
Eady RP (1986) The pharmacology of nedocromil sodium. Eur J Respir Dis 69: (Suppl 147): 112–119
Flint KC, Leung KBP, Oearce FL, Hudspith BN, Brostoff J, Johnson N McI (1985) Human mast cells recovered by bronchoalveolar lavage: their morphology, histamine release and the effects of disodium cromoglycate. Clin Sci 68: 427–432
Johnson HG, Bach MK (1975) Prevention of calcium ionophore-induced release of histamine in rat mast cells by disodium cromoglycate. J Immunol 114: 514–516
Johnston RB, Godzik CA, Cohn ZA (1978) Increased superoxide anion production by immunologically activated and chemically elicited macrophages. J Exp Med 148; 115–127
Kay AB, Walsh GM, Moqbel R. MacDonald AJ, Nagakura T, Carroll MP, Richerson HB (1987) Disodium cromoglycate inhibits activation of human inflammatory cells in vitro. J Allergy Clin Immunol 80: 1–8
Lavens SE, Proud D, Warner JA (1993). A sensitive colorimetric assay for the release of tryptase from human lung mast cells in vitro. J immunol Meth 166: 93–102
Lawrence ID, Warner JA, Cohan VL, Lichtenstein LM, Kagey-Sobotka A, Vavrek JR, Stewart JM, Proud D (1989) Induction of histamine release from human skin mast cells by bradykinin analogs. Biochem Pharmacol 38: 227–233
Otr TSC, Cox JSG (1969) Disodium cromoglycate, an inhibitor of mast cell degranulation and histamine release induced by phospholipase A. Nature 223: 197–198
On TSC, Hall DE, Gwilliam JM, Cox JSG (1971) The effect of sodium cromoglycate on the release of histamine and degranulation of rat mast cells induced by compound 48/80. Life Sci 10: 805–812
Peretti M, Nuti S, Parente L(1990) Investigation of rat mast cell degranulation using flow cytometry. J Pharmacol Meth 23: 187–194
Riley PA, Mather ME, Keogh RW, Eady RP (1987) Activity of nedocromil sodium in mast-cell-dependent reactions in the rat. Int Arch Allergy Appl Immun 82: 108–110
Siriganian RP (1976) Histamine release and assay methods for the study of human allergy. In: Rose NR, Friedman H (eds.) Manual of Clinical Immunology, American Society of Microbiology, Washington. pp 603–615
Skolfitsch G, Saria A, Holzer P, Lembeck F (1981) Histamine in tissue: Determination by high-performance liquid chromatography PLC condensation with o-phthalaldehyde. J Chromatogr. 226: 53–59
Wells E, Jackson CG, Harper ST, Mann J, Eady RP (1986) Characterization of primate bronchoalveolar mast cells. II. Inhibition of histamine, LTC4, and PGD2 release from primate bronchoalveolar mast cells and a comparison with rat peritoneal mast cells. J Immunol 137: 3941–3945
Williams PD, Laska DA, Shetler TJ, McGrath JP, White SL, Hoover DM (1991) Vancomycin-induced release of histamine from rat peritoneal mast cells and a rat basophil cell line (RBL-1). Agents Actions 32: 217–223
Bartlett RR (1986) Immunopharmacological profile of HWA 486, a novel isoxazol derivative-II. in vivo immunomodulating effects differ from those of cyclophosphamide, prednisolone, or cyclosporin A. Int J Immunpharmacol 8: 199–204
di Padova FE (1989) Pharmacology of cyclosporine (Sandimmune) V. Pharmacological effects on immune function: in vitro studies. Pharmacol Rev 41: 373–405
Elves MW (1972) The Lymphocytes, Chapter 7, In vitro lymphocyte transformation and antibody formation. Lloyd Luke Ltd. 2nd ed., pp. 381–457
Sensi M, di Mario U, Pozzilli P (1984) Lymphocyte populations. Evaluation of T and B populations, T cell subpopulations and K cells. In: Lamer J, Pohl SL (eds) Methods in Diabetes Research, Vol I: Laboratory Methods, Part B, John Wiley Sons, New York, pp 77–97
Yamamura M, Nikbin B, Hobbs JR (1976) Standardisation of the mixed lymphocyte reaction. J Immunol Meth 10: 367–378
Zan-Bar I (1983) Modulation of B and T cell subsets in mice treated with fractionated total lymphoid irradiation. I. Blockade of differentiating B cell pathways. Eur J Immunol 13: 35–40
Chong ASF, Finnegan A, Jiang XL, Gebel H, Sanitary HN, Foster P, Williams JW (1993) Leflunomide, a novel immunosuppressive agent. Transplantation 55: 1361–1366
Chong ASF, Gebel H, Finnegan A, Petraitis EE, Jiang XL, Sankary HN, Foster P, Williams JW (1993) Leflunomide, a novel immunomodulatory agent: In vitro analyses of the mechanism of immuno-suppression. Tranplant Proc 25: 747–749
Clipstone NA, Crabtree GR (1993) Calcineurin is a key signaling enzyme in T lymphocyte activation and the target of the immunosuppressive drugs cyclosporin A and FK506. Ann NY Acad Sci 696: 20–30
Dayton JS, Turka LA, Thompson CB, Mitchell BS (1992) Comparison of the effects of mizoribine with those of azathioprine, 6-mercaptopurine, and mycophenolic acid on T lymphocyte proliferation and purine ribonucleotide metabolism. Mol Pharmacol 41: 671–676
di Padova FE (1989) Pharmacology of cyclosporine (Sandimmune) V. Pharmacological effects on immune function: in vitro studies. Pharmacol Rev 41: 373–405
Yamamura M, Nikbin B, Hobbs JR (1976) Standardisation of the mixed lymphocyte reaction. J Immunol Meth 10: 367–378
Zielinski T, Herrmann M, Müller HJ, Riedel N, Bartlett RR (1994) The influence of leflunomide on cell cycle, IL-2receptor (IL-2-R) and its gene expression. Agents Actions 41, Spec Conf Issue: C204 - C205
Zielinski T, Müller HJ, Bartlett RR (1993) Effects of leflunomide (HWA 486) on expression of lymphocyte activation markers. Agents Actions 38, Spec Conf Issue: C80 - C83
Bartlett RR (1986) Immunopharmacological profile of HWA 486, a novel isoxazol derivative-II. in vivo immunomodulating effects differ from those of cyclophosphamide, prednisolone, or cyclosporin A. Int J Immunpharmacol 8: 199–204
Bird J, Giroud JP (1985) An appraisal of the technique of polymorphonuclear leukocyte chemiluminescence as a means to detect compounds with antiinflammatory activity. J Pharmacol Meth 14: 305–312
Johnson Jr RB, Codzik CA, Cohn ZA (1978) Increased superoxide anion production by immunologically activated and chemically elicited macrophages. J Exper. Med. 148: 115–120
Kurosawa M, Hanawa K, Kobayashi S, Nakano M (1990) Inhibitory effects of azelastine on superoxide anion generation from activated inflammatory cells measured by a simple chemiluminescence method. Arzneim Forsch/Drug Res 40: 767–770
Merétey K, Boehm U, Falus A (1983) Chemiluminescence response of human blood mononuclear cells to PAH and histamine. Agents Actions 13: 237–240
Seeds MC, Parce JW, Szeijda P, Bass DA (1985) Independent stimulation of membrane potential changes and the oxidative metabolic burst in polymorphonuclear leukocytes. Blood 65: 233–240
Selvaraj R, Sbarra AJ, Thomas GB, Cetrulo CL, Mitchell GW (1982) A microtechnique for studying chemiluminescence response of phagocytes using whole blood and its application to the evaluation of phagocytes in pregnancy. J Reticutoend Soc 31: 3–16
Weidemann MJ, Smith R, Heaney T, Alaudeen S (1980) On the mechanism of the generation of chemiluminescence by macrophages. Behring Inst. Mitt. 65: 42–54
Weinberg JB, Misokonis MA (1983) Phorbol diester-induced H202 production by peritoneal macrophages. Cell Immun 80: 405–415
Bartlett RR (1986) Immunopharmacological profile of HWA 486, a novel isoxazol derivative — II. in vivo immunomodulating effects differ from those of cyclophosphamide, prednisolone, or cyclosporin A. Int J Immunpharmacol 8: 199–204
Bord JF, Feurer C, Gubler HU, Stähelin H (1976) Biological effects of cyclosporin A: a new antilymphocytic agent. Agents Actions 6: 468–475
Cunningham AJ, Szenberg A (1968) Further improvements in the plaque technique for detecting single antibody forming cells. Immunology 14: 599–608
Stockinger (1978) Negative Rückkoppelungsmechanismen des Immunsystems. Johannes Gutenberg Universität Mainz
Zaalberg (1964) A simple method for detecting single antibody-forming cells. Nature 202: 1231
Barthold DR, Kysela S, Steinberg AD (1974) Decline in suppressor T cell function with age in female NZB mice. J Immunol 112: 9
Bielschowski M, Helyer BJ, Howie JB (1959) Spontaneous anemia in mice of the NZB/BL strain. Proc Univ Otago Med School 37: 9–11
Blanchard D, Bach MA (1980) Thymic function in NZB mice. Clin Exp Immunol 42: 1–9
Cole RK (1966) Hereditary hypothyroidism in domestic fowl. Genetics 13: 1021–1033
Cole RK, Kite JH, Wick G, Witebsky E (1970) Inherited autoimmune thyroiditis in the fowl. Poultry Sci 49: 480–488
Cole RK, Kite JH, Witebsky E (1968) Hereditary autoimmune thyroiditis in the fowl. Science 160: 1357–1358
Field JB (ed) (1983) The juvenile diabetes foundation workshop on the spontaneously diabetic BB rat: its potential for insight into human juvenile diabetes. Metabolism 32 (Suppl 1)
Helyer BW, Howie JB (1963) Renal disease associated with positive lupus erythematosus test in a cross-bred strain of mice. Nature 197: 197
Howie JB, Helyer BJ (1968) The immunology and pathology of NZB mice. In: Advances in Immunology. New York, Academic Press, 9: 215–266
Kessler HS (1968) A laboratory model for Sjögren’s syndrome. Am J Pathol 52: 671–685
Leiter EH, Prochazka M, Coleman DL (1987) Animal model of human disease. The non-obese diabetic ( NOD) mouse. Am J Pathol 128: 380–383
Like AA, Butler L, Williams RM, Appel MC, Weringer EJ, Rossini AA (1982) Spontaneous autoimmune diabetes mellitus in the BB rat. Diabetes 31 (Suppl) 7–13
Makino S, Kunimoto K, Muraoka Y, Mizushima Y, Katagiri K, Tochino Y (1980) Breeding of a non-obese, diabetic strain of mice. Exp Anim 29: 1–13
Miyazaki A, Hanafusa T, Yamada K, Miyagawa J, FujinoKurihara H, Nagajima H, Nonaka K, Tarui S (1985) Predominance of T lymphocytes in pancreatic islets and spleen of pre-diabetic non-obese diabetic (NOD) mice: a longitudinal study. Clin Exp Immunol 60: 622–630
Schuurs AHWM, Verheul HAM, Wick G (1989) Spontaneous autoimmune models. Pharmacological Methods in the Control of Inflammation. pp 449–485, Alan R. Liss, Inc
van Tienhoven A, Cole RK (1962) Endocrine disturbance in obese chickens. Anat Rev 142: 111–122
Wick G, Sundick RS, Albini B (1974) The obese strain (OS) of chickens: an animal model with spontaneous autoimmune thyroiditis. Clin Immunol Immunopathol 3: 272–300
Yale JF, Marliss EB (1984) Altered immunity and diabetes in the BB rat. Clin Exp Immunol 57: 1–11
Austen KF, Brocklehurst WE (1961) Anaphylaxis in chopped guinea pig lung. J Exp Med 113: 521–537
Bhattacharya BK, Delaunois AL (1955) An improved method for the perfusion of isolated lung of guinea pig. Arch Int Pharmacodyn 101: 495–510
Davies GE, Evans (1973) Studies with two new phosphodiesterase inhibitors (ICI 58,301 and ICI 63,197) on anaphylaxis in guinea pigs, mice and rats. Int Arch Allergy 45: 467–478
Elwood W, Lötvall JO, Barnes PJ, Chung KF(1992) Effect of dexamethasone and cyclosporin A on allergen-induced airway hyperresponsiveness and inflammatory cell responses in sensitized Brown-Norway rats. Am Rev Resp Dis 145: 1289–1294
Omote M, Sakai K, Mizusawa H (1994) Acute effects of deflazacort and its metabolite 21-desacetyl-deflezacort on allergic reactions. Arzneim Forsch/Drug Res 44: 149–153
Ufkes JGR, Ottenhof M (1984) Characterization of various antiallergic agents using a new method for inducing systemic anaphylaxis in the rat. J Pharmacol Meth 11: 219–226
Anderson P, Brattsand R (1982) Protective effects of the glucocorticoid, budesonide, on lung anaphylaxis in actively sensitized guinea pigs: Inhibition of the IgE — but not of the IgG — mediated anaphylaxis. Br J Pharmacol 76: 139–147
Austen KF, Brocklehurst WE (1961) Anaphylaxis in chopped guinea pig lung. I. Effect of peptidase substrates and inhibitors. J Exper Med 113: 521–537
Dale HH (1913) The anaphylactic reaction of plain muscle in the guinea-pig. J Pharmacol Exper Ther 4: 167–223
Koppel GA, Haisch KD, Spaethe SM, Schmidtke JR, Fleisch JH (1981) Schultz-Dale reaction in mouse trachea. J Pharmacol Meth 6: 39–43
Laekeman GM, Herman AG, van Nueten JM (1977) Influence of different drugs on the slow response of the intestine during the Schultz-Dale reaction. Arch Int Pharmacodyn 230: 335
Omote M, Sakai K, Mizusawa H (1994) Acute effects of deflazacort and its metabolite 21-desacetyl-deflezacort on allergic reactions. Arzneim Forsch/Drug Res 44: 149–153
Schultz WH (1910) Physiological studies in anaphylaxis. 1. The reaction of smooth muscle of the guinea-pig sensitized with horse serum. J Pharmacol Exper Ther 1: 549–567
Goose J, Blair AMJN (1969) Passive cutaneous anaphylaxis in the rat, induced with two homologous reagin-like antibodies and its specific inhibition with disodium cromoglycate. Immunology 16: 749–760
Griesbacher T, Lembeck F (1987) Actions of bradykinin antagonists on bradykinin-induced plasma extravasation, venoconstriction, prostaglandin E2 release, nociceptor stimulation and contraction of the iris sphincter muscle of the rabbit. Br J Pharmacol 92: 333–340
Katayama S, Shionoya H, Ohtake S (1975) A new simple method for extraction of extravasated dye in the skin. Japan J Pharmacol Suppl 25: 103 P
Patterson R, Talbot CH, Brandfonbrener M (1971) The use of IgE mediated responses as a pharmacologic test system. The effect of disodium cromoglycate in respiratory and cutaneous reactions and in the electrocardiograms of rhesus monkeys. Int Arch Allergy 41: 592–603
Saria A, Lundberg JM, Skofitsch G, Leznbeck F (1983) Vascular protein leakage in various tissues induced by substance P, capsaicin, bradykinin, histamine and by antigen challenge. Naunyn Schmiedeberg’s Arch Pharmacol 324: 212–218
Watanabe N, Ovary Z (1977) Antigen and antibody detection by in vivo methods: a reevaluation of passive cutaneous anaphylactic reactions. J Immunol Meth 14: 381–390
Bartlett RR, Gebert U, v.Kerékjdrtô B, Schleyerbach R, Thor-wart W, Weitmann KU (1989) Substituted 3-phenyl-7Hthiazolo(3,2-b)(1,2,4)triazin-7-ones as antiinflammatory agents with immunomodulating properties. Drugs Exp Clin Res 15: 521–526
Horvat J, Vidic B, Kosec D, Stojic Z, Jankovic BD (1990) Suppression of Arthus and delayed hypersensitivity reactions to bovine serum albumin by dopaminergic antagonists. Period Biol 92: 81–82
Kamei C, Izushi K, Adachi Y, Shimazawa M, Tasaka K (1991) Inhibitory effect of epinastine on the type II—IV allergic reactions in mice, rats and guinea pigs. Arzneim Forsch/Drug Res 41: 1150–1153
Nagakawa Y, Ogawa T, Kobayashi M, Wagatsuma K, Munakata H, Umezu K, Sato S, Shibata Y, Inoue K, Ishida N (1990) Immunopharmacological studies of 4-acetylaminophenylacetic acid. (MS-932),Int J Immunother 6: 131–140
Omote M, Sakai K, Mizusawa H (1994) Acute effects of deflazacort and its metabolite 21-desacetyl-deflezacort on allergic reactions. Arzneim Forsch/Drug Res 44: 149–153
Borel JF (1989) Pharmacology of cyclosporine (Sandimmune) IV. Pharmacological properties in vivo. Pharmacol Rev 41: 259–371
Borel JF, Feurer C, Magnée C, Stähelin H (1977) Effects of the new anti-lymphocytic peptide cyclosporin A in animals. Immunology 32: 1017–1025
Herrmann P, Schreier MH, Borel JF, Feurer C (1988) Mast cell degranulation as a major event in the effector phase of delayed-type hypersensitivity induced by cloned helper cells. Int Arch Allergy Appl Immunol 86: 102–105
Kamei C, Izushi K, Adachi Y, Shimazawa M, Tasaka K (1991) Inhibitory effect of epinastine on the type II—IV allergic reactions in mice, rats and guinea pigs. Arzneim Forsch/Drug Res 41: 1150–1153
Mizukoshi S, Tsukamoto M, Tanaka H, Nakamura K, Kato F (1994) Antiinflammatory and immunosuppressive effects of I,6-anhydro-3,4-dideoxy-2-furfuryl-3-D-rhreo-3-enopyranose (MT 2221), a novel anhydro-enopyranose derivative, on experimental animal models. Biol Pharm Bull 17: 1070–1074
Nagakawa Y, Ogawa T, Kobayashi M, Wagatsuma K, Munakata H, Umezu K, Sato S, Shibata Y, Inoue K, Ishida N (1990) Immunopharmacological studies of 4-acetylaminophenylacetic acid. (MS-932). Int J Immunother 6: 131–140
Titus RG, Chiller JM (1981) A simple and effective method to assess murine delayed type hypersensitivity to proteins. J Immunol Meth 45: 65–78
Berkenkopf JW, Marinari LR, Weichman BM (1991) Phospholipase A2 acyl-hydrolytic activity in rat RPAR-induced pleurisy. Agents Actions 34: 93–96
Berkenkopf JW, Weichman BM (1991) Comparison of several new 5-lipoxygenase inhibitors in a rat Arthus pleurisy model. Eur J Pharmacol 193: 29–34
Burch RM, Connor JR, Bator JM, Weitzberg M, Laemont K, Noronha-Blob L, Sullivan JP, Steranka LR (1992) NPC 15669 inhibits the reverse passive Arthus reaction in rats by blocking neutrophil recruitment. J Pharm Exp Ther 263: 933–937
Camussi G, Tetta C, Bussolino F, Baglioni C (1990) Antiinflammatory peptides (antiflammins) inhibit synthesis of platelet-activating factor, neutrophil aggregation and chemotaxis, and intradermal inflammatory reactions. J Exp Med 171: 913–927
Carter GW, Young PR, Albert DH, Bouska J, Dyer R, Bell RL, Summers JB, Brooks DW (1991) 5-Lipoxygenase inhibitory activity of Zileuton. J Pharm Exp Ther 256: 929–937
Chang YH, Otterness IG (1981) Effects of pharmacologic agents on the reversed passive Arthus reaction in the rat. Eur J Pharmacol 69: 155–164
Humphrey JH (1955 a) The mechanism of Arthus reactions. I. The role of polymorphonuclear leukocytes and other factors in reversed passive Arthus reactions in rabbits. Br J Exp Pathol 36: 268–282
Humphrey JH (1955 b) The mechanism of Arthus reactions. I1. The role of polymorphonuclear leukocytes and platelets in reversed passive Arthus reactions in the guinea-pig. Br J Exp Pathol 36: 283–289
Kim KH, Martin IC, Young PR, Carter GW, Haviv F (1990) Inhibitors of immune complex-induced inflammation: 5-substituted 3-[1-(2-benzoxazolyl)hydrazino]propanenitrile derivatives. J Pharm Sci 79: 682–684
Okamoto H, Iwahisa Y, Terawasa M (1992) Suppression of the Arthus reaction by Y-24180, a potent and specific antagonist of platelet-activating factor. Agents Actions 35: 149–158
Ting PC, Kaminski JJ, Sherlok MH, Tom WC, Lee JF, Bryant RW, Watnick AD, McPhail AT (1990) Substituted 1,3dihydro-2H-pyrrolo[2,3-b]pyridin-2-ones as potential anti-inflammatory agents. J Med Chem 33: 2697–2706
Yamamoto S, Dunn CD, Deporter DA, Capasso F, Willoughby DA, Huskisson EC (1975) A model for the quantitative study of Arthus (immunologic) hypersensitivity in rats. Agents Actions 5: 374–377
Bartlett RR, Schleyerbach R (1985) Immunopharmacological profile of a novel isoxazol derivative, HWA 486, with potential antirheumatic activity. I. Disease modifying action on adjuvant arthritis of the rat, Int J Immunopharmacol 7: 7–18
Beck FWJ, Whitehouse MW, Pearson CM (1974) Drug sensitivity of rat adjuvant arthritis, induced with `adjuvants’ containing no mineral oil components. Proc Soc Exp Biol Med 146: 665–669
Brackertz D, Mitchell GF, MacKay IR (1977) Antigen-induced arthritis in mice. Arthr Rheum 20: 841–850
Colpaert FC (1987) Evidence that adjuvant arthritis in the rat is associated with chronic pain. Pain 28: 201–222
Connolly KM, Stecher VJ, Danis E, Pruden DJ, LaBrie T (1988) Alteration of interleukin-1 production and the acute phase response following medication of adjuvant arthritic rats with cyclosporin-A or methotrexate. Int J Immunopharmac 10: 717–728
Crossley MJ, Holland T, Spowage M, Hunneyball IM (1989) Monarticular antigen-induced arthritis in rabbits and mice. In: Pharmacological Methods in the Control of Inflammation. Alan R Liss, Inc., pp 415–439
Cruwys SC, Garrett NE, Perkins MN. Blake DR, Kidd BL (1994) The role of bradykinin B1 receptors in the maintenance of intra-articular plasma extravasation in chronic antigen-induced arthritis. Br J Pharmacol 113: 940–944
del Pozo E, Graeber M, Payne T (1990) Regression of bone and cartilage loss in adjuvant arthritic rats after treatment with cyclosporin A. Arthr Rheum 33: 247–252
Gardner DL (1960) The experimental production of arthritis. A review. Ann rheum Dis 19: 297–317
Kazuna S, Kawai K (1975) Evaluation of analgesic agents in rats with adjuvant arthritis. Chem Pharm Bull (Tokyo) 23: 1184–1191
Leisten JC, Gaarde WA, Scholz W (1990) Interleukin-6 serum levels correlate with footpad swelling in adjuvant-induced arthritic Lewis rats treated with cyclosporin A or indomethacin. Clin Innnunol Immunopathol 56: 108–115
Mohr W, Wild A (1976) Adjuvant arthritis. Arzneim Forsch/ Drug Res 26: 1860–1866
Pearson CM (1956) Development of’ arthritis, periarthritis and periostitis in rats given adjuvants. Proc Soc Exper Biol Med. 91: 95–101
Pearson CM (1963) Experimental joint disease. Observations on adjuvant-induced arthritis. J Chron Dis 16: 863–874.
Pearson CM, Wood FD (1959) Studies on polyarthritis and other lesions induced in rats by injection of mycobacterium adjuvant. I. General clinic and pathological characteristics and some modifying factors. Arthr Rheum 2: 440–459
Perper RJ, Alvarez B, Colombo C, Schroder H (1971) The use of a standardized adjuvant arthritis assay to differentiate between anti-inflammatory and immunosuppressive agents. Proc Soc Exp Biol Med 137: 506–512
Pircio AW, Fedele CT, Bierwagen ME (1975) A new method for the evaluation of analgesic activity using adjuvant-induced arthritis in the rat. Eur J Pharmacol 31: 207–215
Rooks WH, Tomolonis AJ, Maloney PJ, Wallach MB, Schuler ME (1982) The analgesic and anti-inflammatory profile of (±)-5-benzoyl-1,2-dihydro-3H-pyrrolo[I,2a]pyrrole-1carboxylic acid (RS-37619). Agents Actions 12: 684–690
Sandow J, Alpermann H, Metzger H, Vogel HG (1971) ct-2Glycoprotein levels in the experimental immunoarthritis of the rat. Naunyn-Schmiedeberg’s Arch Pharmacol 269: 483
Schorlemmer HU, Dickneite G (1992) Preclinical studies with 15-deoxyspergualin in various animal models for autoimmune diseases. Ann NY Acad Sci 685: 155–174
Tsurumi K, Kokuba S, Okada K, Yanagihara M, Fujimura H (1986) Pharmacological investigations of the new antiinflammatory agent 2-(10,1 1-dihydro-10-oxodibenzo[b,f]thiepin-2-yl)propionic acid. 4th communication:Inhibitory effects on rat adjuvant arthritis. Arzneim-Forsch/Drug Res 36: 1810–1817
Walz DT, DiMartino MJ, Kuch JH, Zuccarello W (1969) Adjuvant-induced arthritis in rats — Temporal relationship of drug effects on physiological, biochemical, and haematological parameters. Pharmacologist 11: 266
Weichman BM (1989) Rat adjuvant arthritis: A model of chronic inflammation. In: Pharmacological Methods in the Control of Inflammation. Alan R Liss, Inc., pp 363–380
Wilder RL, Allen JB, Hansen C (1987) Thymus-dependent and -independent regulation of la antigen expression in situ by cells in the synovium of rats with streptococcal cell wall-induced arthritis, J Clin Invest 79: 1160–1171
Wilder RL, Calandra GB, Garvin AJ, Wright KD, Hansen CT (1982) Strain and sex variation in the susceptibility to streptococcal wall-induced polyarthritis in the rat. Arthritis Rheum 25: 1064–1072
Yocum DE, Allen JB, Wahl SM, Calandra GB, Wilder RL (1986) Inhibition by cyclosporin A of streptococcal wall-induced arthritis and hepatic granulomas in rats. Arthritis Rheum 29: 262–273
Cannon GW, McCall S, Cole BC, Griffiths MM, Radov LA, Ward JR (1990) Effects of indomethacin, cyclosporin, cyclophosphamide, and placebo on collagen-induced arthritis of mice. Agents Actions 29: 315–323
Carlson RP, Baeder WL, Caccese RG, Warner LM, Sehgal SN (1992) Effects of orally administered rapamycin in animal models of arthritis and other autoimmune diseases. Ann NY Acad Sci 685: 86–113
Henderson H, Staines NA, Burrai I, Cox JH (1984) The anti-arthritic and immunosuppressive effects of cyclosporine on arthritis induced in the rat by type II collagen. Clin Exp Immunol 57: 51–56
Horn JT, Butler LD, Riedl PE, Bendele AM (1988) The progression of the inflammation in established collagen-induced arthritis can be altered by treatments with immunological or pharmacological agents which inhibit T cell activities. Eur J Immunol 18: 881–888
Kaibara N, Hotokebuchi T, Takagishi K, Katsuki I (1983) Paradoxical effects of cyclosporin A on collagen arthritis in rats. J Exp Med 158: 2007–2015
Nemoto K, Mae T, Abe F, Takeuchi T (1992) Successful treatment with a novel immunosuppressive agent, deoxyspergualin, in type II collagen-induced arthritis in mice. Ann NY Acad Sci 685: 148–154
Phadke K, Carroll J, Nanda S (1982) Effects of various anti-inflammatory drugs on type II collagen-induced arthritis in rats. Clin Exp Immunol 47: 579–586
Probeert AW, Schrier DJ, Gilbertsen RB (1984) Effects of antiarthritic compounds on type II collagen-induced arthritis in rats. Arch Int Pharmacodyn 269: 167–176
Takagishi K, Kaibara N, Hotokebuchi T, Arita C, Morinaga M, Arai K (1986) Effects of cyclosporin on collagen induced arthritis in mice. Ann Rheum Dis 45: 339–344
Takagishi K, Yamamoto M, Miyahara H, Hotokebuchi T, Kaibara N (1992) Comparative study of effects of cyclosporins A and G on collagen arthritis in mice. Agents Actions 37: 284–289
Tanaka K, Shimotori T, Makino S, Aikawa Y, Inaba T, Yoshida C, Takano S (1992) Pharmacological studies of the new antiinflammatory agent 3-formylamino-7-methylsulfonylamino-6-phenoxy-4H-l-benzopyran-4-one. 1st Communication: antiinflammatory, analgesic and other related properties. Arzneim Forsch/Drug Res 42: 935–944
Trentham DE, Dynesius-Trentham RA (1989) Type II collagen-induced arthritis in the rat. In: Pharmacological Methods in the Control of Inflammation. Alan R. Liss, Inc., pp 395–413
Trentham DE, Townes AS, Kang AH (1977) Autoimmunity to type II collagen: an experimental model of arthritis. J Exper Med 146: 857–868
Giant TT, Mikecz K, Arzoumanian A, Poole AR (1987)
ProGiant et al (1987, 1992), Mikecz et al (1987, 1990), teoglycan-induced arthritis in BALB/c mice: Clinical fea
Poole (1989) described a proteoglycan-induced pro- tures and histopathology. Arthritis Rheum 30:201–212
Stimpson and Schwab (1989) described a chronic remittent erosive arthritis in rats induced by bacterial peptidoglycan-polysaccharide structures.
Giant TT, Mikecz K, Bartlett RR, Deâk F, Thonar EJMA, Wil- liams JM, Mattar T, Kuettner KE, Schleyerbach R (1992) Immunomodulation of proteoglycan-induced progressive po- lyarthritis by leflunomide. Immunopharmacology 23: 105–116
Hascall VC, Heinegârd D (1974) Aggregation of proteoglycans. I. The role of hyaluronic acid. J Biol Chem 249: 4232–4241
Heinegâard D (1972) Extraction, fractionation and characterization of proteoglycans from bovine tracheal cartilage. Biochim Biophys Acta 285: 181–192
Mikecz K, Giant TT, Bukds E, Poole AR (1990) Proteoglycaninduced polyarthritis and spondylitis adoptively transferred to naive (nonimmunized) BALB/c mice. Arthritis Rheum 33: 866–876
Mikecz K, Giant TT, Poole AR (1987) Immunity to cartilage proteoglycans in BALB/c mice with progressive polyarthritis and ankylosing spondylitis induced by injection of human cartilage proteoglycan. Arthritis Rheum 30: 306–318
Poole AR (1989) Cartilage proteoglycan-induced arthritis: a combined model for rheumatoid arthritis and ankylosing spondylitis. In: Pharmacological Methods in the Control of Inflammation. pp 441–447, Alan R. Liss, Inc
Stimpson AS, Schwab JH (1989) Chronic remittent erosive arthritis induced by bacterial peptidoglycan-polysaccharide structures. In: Pharmacological Methods in the Control of Inflammation. pp 381–394, Alan R. Liss, Inc
Fournier C, Gepner P, Saouk M, Charreire J (1990) In vivo beneficial effects of cyclosporin A and 1,25-dihydroxyvitamin D3 on the induction of experimental autoimmune thyroiditis. Clin Immunol Immunopathol 54: 53–63
Hassman RA, Dieguez C, Rennie DP, Weetman AP, Hall R, McGregor AM (1985) The influence of cyclosporin A on the induction of experimental autoimmune thyroid disease in the PVG/c rat. Clin Exp Immunol 59: 10–16
McGregor AM, Rennie PD, Weetman AP, Hassman RA, Foord SM, Dieguez C, Hall R (1983) The influence of cyclosporin A on experimental autoimmune thyroid disease in the rat. Life Sci 32: 97–108
Penhale WJ, Farmer A, Irvine WJ (1975) Thyroiditis in T cell-depleted rats: influence of strain, radiation dose, adjuvants and antilymphocyte serum. Clin Exp Immunol 21: 362–375
Salamero J, Remy JJ, Michel-Béchet M, Chareire J (1987) Experimental autoimmune thyroiditis induced by a 5–10 kDa cryptic fragment from porcine thyroglobin. Eur J Immunol 17: 843–848
Tamura K, Woo J, Murase N, Nalesnik M, Thomson AW (1993) Inhibitory effect of FK 506 on autoimmune thyroid disease in the PVG rat. Ann NY Acad Sci 696: 257–262
Vladutiu AO (1983) Effect of cyclosporine on experimental autoimmune thyroiditis in mice. Transplantation 35: 518–520
Vladutiu AO, Rose NR (1971) Autoimmune murine thyroiditis relation to histocompatibility (H-2) type. Science 174: 1137–1139
Estrin M, Herzum M, Buie C, Huber SA (1987) Immunosuppressives in murine myocarditis. Eur Heart J 8 (Suppl J) 259–262
Estrin M, Huber SA (1987) Coxsackie virus B3-induced myocarditis. Autoimmunity is L3T4’ T helper cell and IL-2 independent in Balb/c mice. Am J Pathol 127: 337–341
Estrin M, Smith C, Huber S (1986) Coxsackie virus B-3 myocarditis. T-cell autoimmunity to heart antigens is resistant to cyclosporin-A treatment. Am J Pathol 125: 244–251
Huber SA, Lodge PA (1984) Coxsackie virus B-3 myocarditis in Balb/c mice. Evidence for autoimmunity to myocyte antigens. Am J Pathol 116: 21–29
Huber SA, Lodge PA (1986) Coxsackie virus B-3 myocarditis. Identification of different pathogenic mechanisms in DBA/2 and Balb/c mice. Am J Pathol 122: 284–291
Monrad ES, Matsumori A, Murphy JC, Fox JG, Crumpacker CS, Abelmann WH (1986) Therapy with cyclosporine in experimental murine myocarditis with encephalomyocarditis virus. Circulation 7: 1058–1064
O’Connell JB, Reap EA, Robinson JA (1986) The effects of cyclosporine on acute murine Coxsackie B-3 myocarditis. Circulation 73: 353–359
Alvord EC (1984) The challenge: how good a model of MS is EAE today? In: Alvord EC, Kies MW, Suckling AJ (eds) Experimental allergic encephalomyelitis: a useful model for multiple sclerosis. Alan R Liss, New York, pp 3–5
Arnon R (1981) Experimental allergic encephalomyelitis —Susceptibility and suppression. Immunol Rev 55: 5–30
Ben-Nun A, Cohen IR (1982) Experimental autoimmune encephalomyelitis (EAE) mediated by T cell lines: process of selection of lines and characterization of the cells. J Immunol 129: 303–308
Bolton C, Borel JF, Cuzner ML, Davison AN, Turner AM (1982) Immunosuppression by cyclosporin A of experimental allergic encephalomyelitis. J Neur Sci 56: 147–153
Carlson RP, Baeder WL, Caccese RG, Warner LM, Sehgal SN (1992) Effects of orally administered rapamycin in animal models of arthritis and other autoimmune diseases. Ann NY Acad Sci 685: 86–113
Carlson RP, Hartman DA, Tomchek LA, Walter TL, Lugay JR, Calhoun W, Sehgal SN, Chang JY (1993) Rapamycin, a potential disease-modifying antiarthritic drug. J Pharmacol Exp Ther 266: 1125–1138
Chabannes D, Ryffel B, Borel JF (1992) SRI 62–834, a cyclic ether analogue of the phospholipid ET-18-OCH3, displays long-lasting beneficial effects in chronic relapsing encephalomyelitis in the Lewis rat. Comparison with cyclosporin and (Va12)-dihydrocyclosporin effects in clinical, functional and histological studies. J Autoimmun 5: 199–21 I
Feurer C, Chow LH, Borel JF (1988) Preventive and therapeutic effects of cyclosporin and valine2-dihydro-cyclosporin in chronic relapsing experimental allergic encephalomyelitis in the Lewis rat. Immunol 63: 219–223
Hartung HP, Schäfer B, Fierz W, Heininger K, Toyka KV (1987) Cyclosporin A prevents P2 T cell line-mediated experimental autoimmune neuritis ( AT-EAN) in rat. Neurosci Lett 83: 195–200
Hinrichs DJ, Wegmann KW, Peters BA (1983) The influence of cyclosporin A on the development of actively induced and passively transferred experimental allergic encephalomyelitis. Cell Immunol 77: 202–209
King RHM, Craggs RI, Gross MLP, Tompkins C, Thomas PK (1983) Suppression of experimental allergic neuritis by cyclosporin A. Acta Neuropathol (Berl) 59: 262–268
Levine S, Sowinski R (1977) Suppression of the hyperacute form of experimental allergic encephalomyelitis by drugs. Arch Int Pharmacodyn 230: 309–318
McCombe PA, van der Kreek SA, Pender MP (1990) The effects of prophylactic cyclosporin A on experimental allergic neuritis (EAN) in the Lewis rat. Induction of relapsing EAN using low dose of cyclosporin A. J Neuroimmunol 28: 131–140
McFarlin DF, Blank SE, Kibler RF, McKneally S, Shapira R (1973) Experimental allergic encephalomyelitis in the rat: response to encephalitogenic proteins and peptides. Science 179: 478–483
Nakayasu H, Ota K, Tanaka H, Irie H, Takahashi H (1990) Suppression of actively induced and passively transferred experimental allergic neuritis by cyclosporin A. J Neuroimmunol 26: 219–227
Polman CH, Matthaei I, de Groot CJA, Koetsier JC, Sminia T, Dijkstra CD (1988) Low-dose cyclosporin A induces relapsing remitting experimental allergic encephalomyelits in the Lewis rat. J Neuroimmunol 17: 209–216
Rivers TM, Sprunt DH, Berry GP (1933) Observations on attempts to produce acute disseminated encephalomyelitis in monkeys. J Exper Med 58: 39–53
Rosenthale ME, Datko LJ, Kassarich J, Schneider F (1969) Chemotherapy of experimental allergic encephalomyelitis (EAE) Arch Int Pharmacodyn 179: 251–275
Schuller-Levis GB, Kozlowski PB, Wisniewski HM (1986) Cyclosporin A treatment of an induced attack in a chronic relapsing model of experimental allergic encephalomyelitis. Clin Immunol Immunopathol 40: 244–252
Waksman BH, Adams RD (1955) Allergic neuritis: an experimental disease of rabbits induced by the injection of peripheral nervous tissue and adjuvants. J Exp Med 102: 213–234
Waksman BH, Adams RD (1956) A comparative study of experimental allergic neuritis in rabbit, guinea-pig and mouse. J Neuropathol Exp Neurol 15: 293–374
Bartlett RR, Anagnostopulos H, Zielinski T, Mattar T, Schleyerbach R (1993). Effects of leflunomide on immune responses and models of inflammation. Springer Semin Immunopathol 14: 381–394
Bartlett RR, Dimitrijevic M, Mattar T, Zielinski T, Germann T, Riide E, Thoenes G H, Küchle CCA, Schorlemmer HU, Bremer E, Finnegan A, Schleyerbach R (1991). Leflunomide (HWA 486), a novel immunomodulating compound for the treatment of auto-immune disorders and reactions leading to transplantation rejection. Agents and Actions 32: 11–21
Küchle CCA, Thoenes GH, Langer KH, Schorlemmer HU, Bartlett RR, Schleyerbach R (1991). Prevention of kidney and skin graft rejection in rats by leflunomide, a new immunomodulating agent. Transplant Proc 23: 1083–1086
Mrowka C, Thoenes GH, Langer KH, Bartlett RR (1994) Prevention of acute graft versus host disease ( GVHD) in rats by the immunomodulating drug leflunomide. Ann Hematology 68: 195–199
Murase N, Demetris AJ, Woo J, Tanabe M, Furuya T, Todo S, Starzl TE (1993). Graft-versus-host disease after Brown Norway-to-Lewis and Lewis-to-Brown Norway rat intestinal transplantation under FK 506. Transplantation 55: 1–7
Renkonen R, Häyry P (1984). Bone marrow transplantation in the rat. I. Histologic correlation and quantification of cellular infiltrates in acute graft-versus-host disease. Am J Pathol 117: 462–470
Schorlemmer HU, Seiler FR, Bartlett RR (1993). Prolongation of allogenetic transplanted skin grafts and induction of tolerance by leflunomide, a new immunosuppressive isoxyzol derivative. Transplant Proc 25: 763–767
Shaffer D, Muanza T, Blakely M L, Simpson MA, Monaco AP (1993). Prevention of graft-versus-host-disease by RS-61443 in two different rodent models. Transplantation 55: 221–223
Thoenes GH, Sitter T, Langer KH, Bartlett RR, Schleyerbach R (1989). Leflunomide (HWA 486) inhibits experimental autoimmune tubulointerstitial nephritis in rats. Int J Immunopharmacol 11: 921–929
Wakely E, Oberholser JH, Cony RJ (1990) Elimination of acute GVHD and prolongation of rat pancreas allograft survival with DST, cyclosporine, and spleen transplantation. Transplantation 49: 241–245
Bartlett RR, Mattar T, Weithmann U, Anagnostopulos H, Popovic S, Schleyerbach R (1989) Leflunomide (HWA 486): a novel immunorestoring drug. In: Lewis AJ, Doherty NS, Ackerman NR (eds).Therapeutic approaches to inflammatory diseases. New York, Elsevier Science Publishing Co.. Inc., pp 215–228
Bartlett RR, Popovic S, Raiss RX (1988) Development of autoimmunity in MRL/1pr mice and the effect of drugs on this murine disease. Scand. J. Rheumatol. Suppl. 75: 290–299
Carlson RP, Baeder WL, Caccese RG, Warner LM, Sehgal SN (1992) Effects of orally administered rapamycin in animal models of arthritis and other autoimmune diseases. Ann NY Acad Sci 685: 86–113
Gunn HC, Hiestand PC (1988) Cyclosporine A and cyclosporine G enhance IgG rheumatoid factor production in MRL/Ipr Mice. Transplant Proc 20, Suppl 4: 238–242
Schorlemmer HU, Dickneite G (1992) Preclinical studies with 15-deoxyspergualin in various animal models for autoimmune diseases. Ann NY Acad Sci 685: 155–174
Theofilopoulos AN, Dixon FJ (1981) Etiopathogenesis of murine SLE. Immunological Rev 55: 179–216
Damjanovic M, Vidic-Dankovic B, Kosec D, Isakovic K (1993). Thymus changes in experimentally induced myasthenia gravis. Autoimmunity: 15: 201–207
Drachman DB, Adams RN, McIntosh K, Pestronk A (1985) Treatment of experimental myasthenia gravis with cyclosporin A. Clin Immunol Immunopathol 34: 174–188
Itoyama Y, Kira J, Fuji N, Goto I, Yamamoto N (1989). Increases in helper inducer T cells and activated T cells in HTLV-1 associated myelopathy. Ann Neuro1: 26: 257–262
Lennon VA, Lambert EH, Leiby KR, Okarma TB, Talib S (1991). Recombinant human acetylcholine receptor a-subunit induces chronic experimental autoimmune myasthenia gravis. J Immunol, 146: 2245–2248
McIntosh KR, Drachman DB (1986) Induction of suppressor cells specific for AChR in experimental autoimmune myasthenia gravis. Science 232: 401–403
McIntosh KR, Drachman DB (1987) Properties of suppressor cells induced to acetylcholine receptor using cyclosporin A. Ann NY Acad Sci 505: 628–638
Mrowka C, Thoenes GH, Langer KH, Bartlett RR (1994) Prevention of acute graft versus host disease ( GVHD) in rats by the immunomodulating drug leflunomide. Ann Hematology 68: 195–199
Norcross NL, Griffith IJ, Lettieri JA (1980). Measurement of acetylcholine receptors and anti-receptor antibodies by ELISA. Muscle Nerve 3: 345–349
Oosterhuis H (1981). Observations of the natural history of myasthenia gravis and effect of thymectomy. Ann NY Acad Sci 377: 678–682
Ulrichs, K., Kaitschick, J., Bartlett, R., Müller-Ruchholtz, W. (1992) Suppression of natural xenophile antibodies with the novel immunosuppressive drug leflunomide. Transplant. Proc. 24: 718–719
Williams JW, Xiao F, Foster P, Clardy C, McChesney L, Sankary H, Chong ASF (1994) Leflunomide in experimental transplantation. Control of rejection and alloantibody production, reversal of acute rejection, and interaction with cyclosporine. Transplantation 57: 1223–1231
Aten J, Bosman CB, de Heer E, Hoedemaeker PJ, Weening JJ (1988) Cyclosporin A induces long-term unresponsiveness in mercuric chloride-induced autoimmune glomerulonephritis. Clin exp Immunol 73: 307–311
Baran D, Vendeville B, Vial MC, Cosson C, Bascou C, Teychenne P, Druet P (1986) Effect of cyclosporin A on mercury-induced autoimmune glomerulonephritis in the Brown Norway rat. Clin Nephrol 25, Suppl 1: S175 — S180
Cattran DC (1988) Effect of cyclosporin on active Heymann nephritis. Nephron 48: 142–148
Fujita M, Ilida H, Asaka M, Izumino K, Takata M, Sasayama S (1991) Effect of the immunosuppressive agent, cyclosporin, on experimental immune complex glomerulonephritis in rats. Nephron 57: 210–205
Giménez A, Leyva-Cobian F, Fiero C, Rio M, Bricio T, Mampaso F (1987) Effect of cyclosporin A on autoimmune tubulointerstitial nephritis in the brown Norway rat. Clin exp Immunol 69: 550–556
Grönhagen-Riska C, von Willebrand E, Tikkanen T, Honkanen E, Miettinen A, Holthöfer H, Törnroth T (1990) The effect of cyclosporin A on the interstitial mononuclear cell infiltration and the induction of Heymann’s nephritis. Clin exp Immunol 79: 266–272
Heymann W, Hackel DB, Harwood S, Wilson SGF, Hunter JLP (1959) Production of nephrotic syndrome in rats by Freund’s adjuvants and rat kidney suspension. Proc Soc Exp Biol Med 100: 660–664
Ito M, Yamada H, Okamoto K, Suzuki Y (1983) Crescentic type nephritis induced by anti-glomerular basement membrane ( GMB) serum in rats. Jap J Pharmacol 33: 1145–1154
Kokui K, Yoshikawa N, Nakamura H, Itoh H (1992) Cyclosporin reduces proteinuria in rats with aminonucleoside nephrosis. J Pathol 166: 297–301
Lillevang ST, Rosenkvist J, Andersen CB, Larsen S, Kemp E, Kristensen T (1992) Single and combined effects of the vitamin D analogue KH1060 and cyclosporin A on mercuricchloride-induced autoimmune disease in the BN rat. Clin exp Immunol 88: 301–306
Ogawa T, Inazu M, Gotoh K, Hayashi S (1990) Effects of leflunomide on glomerulonephritis induced by antibasement membrane antibody in rats. Agents Actions 31: 321–328
Ogawa T, Inazu M, Gotoh K, Inoue T, Hayashi S (1991) Therapeutic effects of leflunomide, a new antirheumatic drug, on glomerulonephritis induced by the antibasement antibody in rats. Clin Immunol Immunopathol 61: 103–118
Reynolds J, Cashman SJ, Evans DJ, Pusey CD (1991) Cyclosporin A in the prevention and treatment of experimental autoimmune glomerulonephritis in the brown Norway rat. Clin Exp Immunol 85: 28–32
Schorlemmer HU, Dickneite G (1992) Preclinical studies with 15-deoxyspergualin in various animal models for autoimmune diseases. Ann NY Acad Sci 685: 155–174
Shibata S, Nagasawa T, Takuma T, Naruse T, Miyakawa Y, (1966) Isolation and properties of the soluble antigen specific for the production of nephrotoxic glomerulonephritis. I. Immunopathological demonstration of the complete antigenicity of the soluble antigen. Jpn J Exp Med 36: 127–143
Shih W, Hines WH, Neilson EG (1988) Effects of cyclosporin A on the development of immune-mediated interstitial nephritis. Kidney Internat 33: 1113–1118
Thoenes GH, Sitter T, Langer KH, Bartlett RR, Schleyerbach R (1989) Leflunomide (HWA 486) inhibits experimental autoimmune tubulointerstitial nephritis in rats. Int J Immunopharmac 11: 921–929
Thoenes GH, Umscheid T, Sitter T, Langer KH (1987) Cyclosporin A inhibits autoimmune experimental tubulointerstitial nephritis. Immunol Lett 15: 301–306
Tipping PG, Holdsworth SR (1985) Effect of cyclosporin A on antibody-induced experimental glomerulonephritis. Nephron 40: 201–205
Tipping PG, Neale TJ, Holdsworth SR (1985) T lymphocyte participation in antibody-induced experimental glomerulonephritis. Kidney Internat 27: 530–537
Wilson CB (1981) Nephritogenic antibody mechanisms involving antigens within the glomerulus. Immunol Rev 55: 257–297
Wood A, Adu D, Birtwistle RJ, Brewer DB, Michael J (1988) Cyclosporin A and anti-glomerular basement membrane antibody glomerulonephritis in rats. Br J Path 69: 189–193
Brockhuyse RM, Kuhlmann EC, van Vugt AHM, Winkens Hi (1987) Immunological and immunopathological aspects of opsin-induced uveoretinitis. Graefe’s Arch Clin Exp Ophthalmol 225: 45–49
Caspi RR, McAllister CG, Gery I, Nussenblatt RB (1988) Differential effects of cyclosporins A and G on functional activation of a T-helper-lymphocyte line mediating experimental autoimmune uveoretinitis. Cell Immunol 113: 350–360
Chan CC, Caspi R, Mochizuki M, Diamantstein T, Gery I, Nussenblatt RB (1987) Cyclosporine and dexamethasone inhibit T-lymphocyte MHC class II antigens and IL-2 receptor expression in experimental autoimmune uveitis. Immunol Invest 16: 319–331
Chan CC, Palestine AG, Nussenblatt RB (1984) Cyclosporineinduced alterations of humoral response in experimental autoimmune uveitis. Invest Ophthalmol Vis Sci 25: 867–870
de Kozak Y, Sakai J, Thillaye B, Faure JP (1982) S antigen-induced experimental autoimmune uveo-retinitis in rats. Curr Eye Res 1: 327–337
Fujino Y, Okumura A, Nussenblatt RB, Gery I, Mochizuki M (1988) Cyclosporine-induced specific unresponsiveness to retinal soluble antigen in experimental autoimmune uveoretinitis. Clin Immunol Immunopathol 46: 234–248
Jamieson L, Meckoll-Brinck D, Keller N (1989) Characterized and predictable rabbit uveitis model for antiinflammatory drug screening. J Pharmacol Meth 21: 329–338
Kaswan RL, Kaplan RI (1988) Comparison of the efficacy of unilateral, bilateral, and oral cyclosporine in experimental immunogenic uveitis in rabbits. Transplant Proc 20, Suppl 4: 149–157
Liversidge J, Thompson AW, Sewell HF, Forrester JV (1987) EAU in the guinea pig: inhibition of cell-mediated immunity and Ia antigen expression by cyclosporin A. Clin exp Immunol 69: 591–600
Liversidge J, Thomson AW, Sewell HF, Forrester JV (1988) Cyclosporine A, experimental autoimmune uveitis, and major histocompatibility class II antigen expression of cultured retinal pigment epithelial cells. Transplant Proc 20, Suppl 4: 163–169
Mahlberg K, Uusitalo H, Uusitalo R, Palkama A, Tallberg T (1987) Suppression of experimental autoimmune uveitis in guinea pigs by ethylenediamine tetra-acetic acid, corticosteroids and cyclosporin. J Ocul Pharmacol 3: 199–210
Mochizuki M, Nussenblatt RB, Kuwabara T, Gery I (1985) Effects of cyclosporine and other immunosuppressive drugs on experimental autoimmmune uveoretinitis in rats. Invest Ophthalmol Vis Sci 26: 226–232
Nordmann JP, de Kozak Y, Le Hoang P, Faure JP (1986) Cyclosporine therapy of guinea-pig autoimmune uveitis induced with autologous retina. J Ocul Pharmacol 2: 325–333
Nussenblatt RB, Rodrigues MM, Wacker WB, Cevario SJ, Salinas-Carmona MC (1981) Inhibition of experimental autoimmune uveitis in Lewis rats. J Clin Invest 67: 1228–1231
Smith-Lang L, Glaser RL, Miller ST, Weimer LK, Robertson SM, Aoki KR, Yanni JM (1992) Efficacy of novel immunomodulators leflunomide and rapamycin in autoimmune uveitis. FASEB J 6:A1048, Part 1
Wacker WB, Lipton MM (1965) Experimental allergic uveitis: homologous retina as uveitigenic antigen. Nature 206: 253–254
Wacker WB, Lipton MM, Ongchua FE (1964) Antibody production in the guinea pig to homologous uvea. Proc Soc Exp Biol Med 117: 150–154
Adams DH, Tiney NL, Collins JJ, Karnovsky MJ (1992) Experimental graft arteriosclerosis. Transplantation 53: 11 15 1119
Almond PS, Moss A, Nakhleh R, Melin M, Chen S, Salazar A, Shirabe K, Matas A (1992) Rapamycin in a renal transplant model. Ann NY Acad Sci 685: 121–122
Bartlett RR, Dimitrijevic M, Mattar T, Zielinski T, Germann T, Rüde E, Thoenes G H, Küchle CCA, Schorlemmer HU, Bremer E, Finnegan A, Schleyerbach R (1991). Leflunomide (HWA 486), a novel immunomodulating compound for the treatment of auto-immune disorders and reactions leading to transplantation rejection. Agents and Actions 32: 11–21
Coupland SE, Klebe S, Karow AC, Krause L, Kruse H, Bartlett RR, Hoffmann F (1994) Leflunomide therapy following penetrating keratoplasty in the rat. Graefe’s Arch Clin Exp Ophthalmol 232: 622–627
Cramer DV, Chapman FA, Wu GD, Harnaha JB, Qian S, Makowka L (1990) Cardiac transplantation in the rat. Transplantation 50: 554–558
Davreux CJ, Chu NH, Waddell TK, Mayer E, Patterson GA (1993) Improved tracheal allograft viability in immunosuppressed rats. Ann Thorac Surg 55: 131–134
de Masi R. Algaisi M, Araneda D, Nifong W, Thomas J, Gross U, Swanson M, Thomas F (1990) Reevaluation of total-lymphoid irradiation and cyclosporine therapy in the Syrian hamster-to-Lewis rat cardiac xenograft model. Transplantation 49: 639–641
Engelbrecht G, Kahn D, Duminy F, Hickman R (1992) New rapid technique for renal transplantation in the rat. Microsurg 13: 340–344
Fujino Y, Kawamura T, Hullett DA, Sollinger HW (1994) Evaluation of cyclosporine, mycophenolate mofetil, and brequinar sodium combination therapy on hamster-to-rat cardiac xenotransplantation. Transplantation 57: 41–46
Hancock WW, diStefano R, Braun P, Schweizer RT, Tilney NL, Kupiec-Weglinski JW (1990) Cyclosporin and antiinterleukin 2 receptor monoclonal antibody therapy suppress accelerated rejection of rat cardiac allografts through different effector mechanisms. Transplantation 49: 416–421
Kahn DR, Forrest DE, Otto DA (1991) Prolonged survival of rat cardiac allografts by donor pretreatment with methotrexate. Transplantation 51: 697–700
Katayama Y, Yada I, Namikawa S, Kusagawa M (1991) Immunosuppressive effects of FK 506 in rat lung transplantation. Transplant Proc 23: 3300–3301
Kellnar S, Herkomer C, Bae S, Schumacher U (1990) Allogenic transplantation of fetal rat intestine: anastomosis to the normal bowel of the host. J Pediatr Surg 25: 415–417
Kirsch AJ, Kirsch SS, Kimura K, LaRosa CA, Jaffe BM (1991) The adaptive ability of transplanted rat small intestine. Surgery 109: 779–787
Kobayashi J, Mavroudis C, Crawford SE, Zales VR, Backer CL (1993) A new rat infection-heart transplant model: effect of infection on graft survival studies. J Heart Lung Transplant 12: 659–664
Küchle CCA, Thoenes GH, Langer KH, Schorlemmer HU, Bartlett RR, Schleyerbach R (1991). Prevention of kidney and skin graft rejection in rats by leflunomide, a new immunomodulating agent. Transplant Proc 23: 1083–1086
Kuroki H, Ishida O, Daisaku H, Fukuhara K, Hatano E, Murakami T, Ikuta Y, Matsumoto AK, Akiyama M (1991) Morphological and immunological analysis of rats with long-term-surviving limb allografts induced by a short course of FK 506 or cyclosporine. Transplant Proc 23: 516–520
Langrehr JM, Hoffman RA, Banner B, Stangl MJ, Monyhan H, Le KKW, Schraut WH (1991) Induction of graft-versushost disease and rejection by sensitized small bowel allografts. Transplantation 52: 399–405
Lee WP, Pan YC, Kesmarky S, Randolph MA, Fiala TS, Amarante MTJ, Weiland AJ, Yaremchuk MJ (1995) Experimental orthotopic transplantation of vascularized skeletal allografts: functional assessment and long-term survival. Plast Reconstr Surg 95: 336–353
McManus RP, O’Hair DP, Komorowski R, Scott JP (1993) Immunosuppressant combinations in primate cardiac xenografts. Ann NY Acad Sci 969: 281–284
Mennander A, Tiisala S, Paavonen T, Halttunen J, Häyry P (1991). Chronic rejection of rat aortic allograft. II. Administration of cyclosporin induces accelerated allograft arteriosclerosis. Transplant Int 4: 173–179
Muramatsu K, Doi K, Kawai S (1994) The outcome of neurovascularized allogeneic muscle transplantation under immunosuppression with cyclosporine. J Reconstr Microsurg 10: 77–81
Murase N, Demetris A J, Woo J, Tanabe M, Furuya T, Todo S, Strazl T E (1993). Graft-versus-host disease after Brown Norway-to-Lewis and Lewis-to-Brown Norway rat intestinal transplantation under FK 506. Transplantation 55: 1–7
Nemoto K, Sugawara Y, Mae T, Hayashi M, Abe F, Fujii A, Takeuchi T (1992) Therapeutic activity of deoxyspergualin in comparison with cyclosporin A, and its combined use with cyclosporin A and prednisolone in highly allogeneic skin transplantation in the rat. Agents Actions 36: 306–311
Schorlemmer HU, Seiler FR, Bartlett RR (1993). Prolongation of allogenetic transplanted skin grafts and induction of tolerance by leflunomide, a new immunosuppressive isoxyzol derivative. Transplant Proc 25: 763–767
Schuurman HJ, Joergensen J, Kuipers H, Meerloo T, Lardelli P, Hiestand P, White DH, Schreier MH (1994) Vascular transplantation of Syrian hamster heart into Lewis rat: effect of brequinar, cyclosporine, cobra venom factor, and splenectomy. Transplant Proc 26: 1217–1219
Shaffer D, Muanza T, Blakely M L, Simpson M A, Monaco A P (1993). Prevention of graft-versus-host-disease by RS-61443 in two different rodent models. Transplantation 55: 221–223
Steinbrüchel DA, Madsen HH, Nielsen B, Kemp E, Larsen S, Koch C (1991) The effect of combined treatment with total lymphoid irradiation, cyclosporin A, and anti-CD4 monoclonal antibodies in a hamster-to-rat heart transplantation model. Transplant Proc 23: 579–580
Svensson G, Holmberg SB, Friman S (1995) Influence of liver transplantation and cyclosporin on bile secretion — an experimental study in the rat. Transpl Int 8: 27–34
Ulrichs, K., Kaitschick, J., Bartlett, R., Muller-Ruchholtz, W. (1992) Suppression of natural xenophile antibodies with the novel immunomodulating drug leflunomide. Transplant. Proc. 24: 718–719
van den Bogaerde J, Aspinall R, Wang MW, Cary N, Lim S, Wright L, White D (1991) Induction of long-term survival of hamster heart xenografts in rats. Transplantation 52: 15–20
Walpoth BH, Tschopp A, Lazeyras F, Galdikas J, Tschudi J, Altermatt H, Schaffner T, Aue WP, Althaus U (1993) Magnetic resonance spectroscopy for assessing myocardial rejection in the transplanted rat heart. J Heart Lung Transplant 12: 271–282
Williams JW, Xiao F, Foster P, Chong A, Sharma S, Bartlett RR, Sankary HN (1993) Immunosuppressive effects of leflunomide in a cardiac allograft model. Transplant Proc 25: 745–746
Williams JW, Xiao F, Foster P, Clardy C, McChesney L, Sankary H, Chong ASF (1994) Leflunomide in experimental transplantation. Control of rejection and alloantibody production, reversal of acute rejection, and interaction with cyclosporine. Transplantation 57: 1223–1231
Woo J, Valdivia LA, Pan F, Celli S, Fing JJ, Thomson AW (1993) Cytidine potentiates the inhibitory effect of brequinar sodium on xeno-MLR, antibody production, and concordant hamster to rat cardiac xenograft survival. Ann NY Acad Sci 969: 227–234
Xia W, Kirkman RL (1990), Immune function in transplanted small intestine. Transplantation 49: 277–280
Xiao F, Chong ASF, Bartlett RR, Williams JW (1994) Leflunomide: a promising immunosuppressant in transplantation. In: Thomson AW, Starzl ThE (eds) Immunosuppressive Drugs. Edward Arnold, London, Boston, Melbourne, pp 203–212
Yu LT, England J, Sumner A, Larossa D, Hickey WF (1990) Electrophysiologic evaluation of peripheral nerve regeneration through allografts immunosuppressed with cyclosporin. J Reconstr Microsurg 6: 317–323
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Vogel, H.G., Vogel, W.H. (1997). Anti-arthrotic and immunmodulatory activity. In: Vogel, H.G., Vogel, W.H. (eds) Drug Discovery and Evaluation. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-03333-3_9
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