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Comparison of adjuvant and streptococcal cell wall-induced arthritis in the rat

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In Vivo Models of Inflammation

Abstract

The goals of this chapter are to discuss rat adjuvant and streptococcal cell wall-induced arthritis, both as animal models of chronic inflammation, and as relevant and predictive models of human rheumatoid arthritis (RA). The information which follows is intended to (1) provide the investigator with a detailed methodology for these two chronic models of inflammation, and (2) to review the pathogenesis and therapeutic interventions for which these models have historically been used to further our understanding of RA and its potential regulation by novel drugs. While these animal models have been extensively studied for over 30 years, the following information provides a rationale to better understand the similarities and differences of these models to RA. Furthermore, this chapter will describe how new technologies, such as magnetic resonance imaging (MRI), can be integrated with these “old” models to better predict clinical efficacy with the many new biological and immunomodulatory drugs currently in development.

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References

  1. Stoerk HC, Bielinski TC, Budzilovich T (1954) Chronic polyarthritis in rats injected with spleen in adjuvants. Am J Pathol 30: 616–621

    Google Scholar 

  2. Pearson CM (1956) Development of arthritis, periarthritis and periostitis in rats given adjuvants. Proc Soc Exp Biol Med 91: 95–101

    CAS  PubMed  Google Scholar 

  3. Pearson CM, Wood FD (1959) Studies of polyarthritis and other lesions induced in rats by injection of mycobacterial adjuvant. I. General clinical and pathologic characteristics and some modifying factors. Arth Rheum 2: 440–449

    Article  Google Scholar 

  4. Newbould BB (1963) Chemotherapy of arthritis induced by rats by injection of mycobacterial adjuvant. Br J Pharmac 21: 127–136

    CAS  Google Scholar 

  5. Winter CA, Nuss GW (1966) Treatment of adjuvant arthritis in rats with anti-inflammatory drugs. Arth Rheum 9: 394–404

    Article  CAS  Google Scholar 

  6. Glenn EM (1966) Adjuvant-induced arthritis: effects of certain drugs on incidence, chemical severity and biochemical changes. Am J Vet Res 27: 339–352

    CAS  PubMed  Google Scholar 

  7. Ward JR, Cloud RS (1966) Comparative effect of antirheumatic drugs on adjuvant-induced polyarthritis in rats. J Pharmacol Exp Ther 152: 116–121

    CAS  PubMed  Google Scholar 

  8. Graeme ML, Fabry E, Sigg EB (1966) Mycobacterial adjuvant periarthritis in rodents and its modification by anti-inflammatory agents. J Pharmacol Exp Ther 153: 373–380

    CAS  Google Scholar 

  9. Waltz DT, Dolan MM, DiMartino MJ, Yankell SL (1971) Effects of topical hydrocortisone and acetylsalicylic acid on the primary lesion of adjuvant-induced arthritis (35811). Proc Soc Exp Biol Med 137: 1466–1469

    Google Scholar 

  10. Waltz DT, DiMartino MJ, Misher A (1971) Adjuvant-induced arthritis in rats. II. Drug effects on physiologic, biochemical and immunologic parameters. J Pharmacol Exp Therap 178: 223–231

    Google Scholar 

  11. Perrin JW, Takesue EI (1968) Use of the rotarod in determining grip strength in rats with adjuvant-induced arthritis. Arch Int Pharmacodyn Ther 174: 192–198

    Google Scholar 

  12. Billingham MEJ, Gordon AH (1976) Changes in concentration and synthesis rates of plasma proteins during experimental arthritis. In: H Peters (ed): Protides of the biological fluids. Elsevier, Amsterdam, 451–454

    Google Scholar 

  13. Baumgartner WA, Beck FWJ, Lorber A, Pearson CM, Whitehouse MW (1974) Adjuvant disease in rats: biochemical criteria for distinguishing several phases of inflammation and arthritis. Proc Soc Exp Biol Med 145: 625–630

    CAS  PubMed  Google Scholar 

  14. Blackham A, Burns JW, Farmer JB, Radziwonik H, Westwick J (1977) An x-ray analysis of adjuvant arthritis in the rat. The effect of prednisolone and indomethacin. Agents and Actions 7: 145–151

    Article  CAS  PubMed  Google Scholar 

  15. Wilcox DM, Nuss ME, Morgan SJ, Harris RR, Carlson RP, Bell RL, Summers JB, Jacobson PB (1996) Therapeutic evaluation of selective cyclooxygenase-2 inhibitors in rat established adjuvant arthritis by magnetic resonance imaging and inflammatory parameters. Arth Rheum 39: S285

    Google Scholar 

  16. Jacobson PB, Wilcox DM, Morgan SJ, Carlson RP, Harris RR (1996) Antiarthritic activities of orally administered FK-506, rapamycin, and combinational therapy in rat established adjuvant arthritis. Arth Rheum 39: S246

    Google Scholar 

  17. Van Arman CG (1976) Pathway to adjuvant arthritis. Fed Proc 35: 2442–2446

    PubMed  Google Scholar 

  18. Mohr W, Wild A (1976) Adjuvant arthritis. Arzneim Forsch 26: 1860–1866

    CAS  Google Scholar 

  19. Billingham MEJ, Davies GE (1978) Experimental models of arthritis in animals as screening tests for drugs to treat arthritis in man. In: J Vane (ed): Inflammation handbook of experimental pharmacology. Springer, Berlin, 108–144

    Google Scholar 

  20. Owen RT (1980) Adjuvant induced polyarthritis-an overview. Meth Find Exp Clin Pharmacol 2: 199–204

    CAS  Google Scholar 

  21. Billingham MEJ (1983) Models of arthritis and the search for antiarthritic drugs. Pharmacol Ther 21: 389–428

    Article  CAS  PubMed  Google Scholar 

  22. Lewis AJ, Carlson RP, Chang JY (1985) Experimental models of inflammation. In: IL Bonta, MA Bray, MJ Parnham (eds): Handbook of inflammation. Elsevier, Amsterdam, 371–397

    Google Scholar 

  23. Rook GAW (1988) Rheumatoid arthritis, mycobacterial antigens, and agalactosyl IgG. Scand J Immunol 28: 487–493

    Article  CAS  PubMed  Google Scholar 

  24. Billingham MEJ (1995) Adjuvant Arthritis: the first model. In: B Henderson, JCW Edwards, ER Pettipher (eds): Mechanisms and models in rheumatoid arthritis. Academic Press, London, 389–409

    Chapter  Google Scholar 

  25. Schwab JH, Cromartie WJ, Robertson BS (1959) Identification of a toxic cellular component of group A streptococci as a complex of group-specific C polysaccharide and a protein. J Exp Med 109: 43–54

    Article  CAS  PubMed  Google Scholar 

  26. Cromartie WJ, Craddock JG (1966) Rheumatic-like cardiac lesions in mice. Science 154: 285–287

    Article  CAS  PubMed  Google Scholar 

  27. Schwab JH, Cromartie WJ, Ohanian SH, Craddock JG (1967) Association of experimental chronic arthritis with the persistence of Group A streptococcal cell walls in the articular tissue. J Bacteriol 94: 1728–1735

    CAS  PubMed  Google Scholar 

  28. Cromartie WJ, Craddock JG, Schwab JH (1968) Production of chronic arthritis in rats with Group A streptococcal cellular components. Fed Proc 27: 477

    Google Scholar 

  29. Cromartie WJ, Craddock JG, Schwab JH, Anderle SK, Yang CH (1977) Arthritis in rats after systemic injection of streptococcal cells or cell walls. J Exp Med 146: 1585–1602

    Article  CAS  PubMed  Google Scholar 

  30. Wilder RL, Allen JB, Wahl LM, Calandra GB, Wahl SM (1983) The pathogenesis of group A streptococcal cell wall induced polyarthritis in the rat. Comparative studies in arthritis resistant and susceptible strains. Arth Rheum 26: 1442–1451

    Article  CAS  Google Scholar 

  31. Spitznagel JK, Goodrum KJ, Warejcka DJ (1983) Rat arthritis due to whole group B streptococci. Clinical and histopathologic features compared with groups A and D. Am J Pathol 112: 37–47

    CAS  PubMed  Google Scholar 

  32. Ridge SC, Zabriske JB, Oronsky AL, Kerwar SS (1985) Streptococcal cell wall arthritis: studies with nude (athymic) inbred Lewis rats. Cell Immunol 96: 231–234

    Article  CAS  PubMed  Google Scholar 

  33. Wells A, Pararajasegaram G, Balwin M, Yang CH, Hammer M, Fox A (1986) Uveitis and arthritis induced by systemic injection of streptococcal cell walls. Invest Opthalmol Vis Sci 27: 921–925

    CAS  Google Scholar 

  34. Wahl SM, Hunt DA, Allen JB, Wilder RL, Paglia L, Hand AR (1986) Bacterial cell wall-induced hepatic granulomas. An in vivo model of T cell-dependent fibrosis. J Exp Med 163: 884–902

    Article  CAS  PubMed  Google Scholar 

  35. Sartor RB, Cromartie WJ, Powell DW, Schwab JH (1985) Granulomatous enterocolitis induced in rats by purified bacterial cell wall fragments. Gastroenterology 89: 587–595

    CAS  PubMed  Google Scholar 

  36. Sartor RB, Anderle SK, Cromartie WJ, Schwab JH (1986) Localized gut-associated lymphoid tissue hemorrhage induced by intravenous peptidoglycan-polysaccharide polymers. Infect Immun 51: 521–528

    CAS  PubMed  Google Scholar 

  37. Severijnen AJ, Hazenberg MP, van de Merwe JP (1988) Induction of chronic arthritis in rats by cell wall fragments of anaerobic coccoid rods isolated from the faecal flora of patients with Crohn’s disease. Digestion 39: 118–125

    Article  CAS  PubMed  Google Scholar 

  38. Severijnen AJ, Kool J, Swaak AJG, Hazenberg MP (1990) Intestinal flora of patients with rheumatoid arthritis: induction of chronic arthritis in rats by cell wall fragments from isolated Eubacterium aerofaciens strains. Br J Rheumatol 29: 433–439

    Article  CAS  PubMed  Google Scholar 

  39. Schwab JH (1993) Phlogistic properties of peptidoglycan-polysaccharide polymers from cell walls of pathogenic and normal-flora bacteria which colonize humans. Infect Immun 61: 4535–4539

    CAS  PubMed  Google Scholar 

  40. Esser RE, Stimpson SA, Anderle SK, Eisenberg RA, Brown RR, Cromartie WJ, Schwab JH (1985) Mechanisms of recurrence in bacterial cell wall-induced arthritis. In: Y Kimura, S Kotani, Y Shiokawa (eds): Recent advances in streptococci and streptococcal diseases. Reedbooks, Bracknell, UK, 351–352

    Google Scholar 

  41. Vernon-Roberts B, Liyanage SP, Currey HLF (1975) Adjuvant arthritis in the rat. Distribution of fluorescent material after footpad injection of rhodamine-labelled tubercle bacilli. Ann Rheum Dis 35: 389–397

    Article  CAS  PubMed  Google Scholar 

  42. DeJoy SQ, Ferguson-Chanowitz KF, Oronsky AL, Zabriskie JB, Kerwar SS (1990) Studies on the homing of Mycobacterium-sensitized T lymphocytes to the synovium during passive adjuvant arthritis. Cell Immun 130: 195–203

    Article  CAS  Google Scholar 

  43. Anderle SK, Allen JB, Wilder RL, Eisenberg RA, Cromartie WJ, Schwab JH (1985) Measurement of streptococcal cell wall in tissues of rats resistant or susceptible to cell wall-induced chronic erosive arthritis. Infect and Immun 49: 836–837

    CAS  Google Scholar 

  44. Wilder RL, Allen JB (1985) Regulation of susceptibility to bacterial cell wall-induced arthritis in rats. Arth Rheum 28: 1318–1319

    Article  CAS  Google Scholar 

  45. Busso N, So A (1997) Urokinase in rheumatoid arthritis: causal or coincidental? Ann Rheum Dis 56: 705–706

    Article  CAS  PubMed  Google Scholar 

  46. Holoshitz JA, Matitiau A, Cohen IR (1984) Arthritis induced in rats by cloned T-lymphocytes responsive to mycobacteria but not to collagen type II. J Clin Invest 73: 211–215

    Article  CAS  PubMed  Google Scholar 

  47. Whitehouse DJ, Whitehouse MW, Pearson CM (1969) Passive transfer of adjuvant-induced arthritis and allergic encephalomyelitis in rats using thoracic duct lymphocytes. Nature 224: 1322

    Article  CAS  PubMed  Google Scholar 

  48. Taurog JD, Sandberg GP, Mahowald ML (1983) The cellular basis of adjuvant arthritis. II. Characterization of the cells mediating passive transfer. Cell Immunol 80: 198–204

    Article  CAS  PubMed  Google Scholar 

  49. Fassbender HG (1994) Inflammatory reactions in arthritis. In: ME Davies, JT Dingle (eds): Immunopharmacology of joints and connective tissue. Academic Press, London, 165–198

    Google Scholar 

  50. Rainsford KD (1982) Adjuvant polyarthritis in rats: is this a satisfactory model for screening anti-arthritic drugs? Agents and Actions 12: 452–458

    Article  CAS  PubMed  Google Scholar 

  51. Philippe L, Gegout-Pottie G, Guingamp C, Bordji K, Terlain B, Netter P, Gillet P (1997) Relations between functional, inflammatory, and degenerative parameters during adjuvant arthritis in rats. Am J Physiol 273: R1550 — R1556

    CAS  PubMed  Google Scholar 

  52. Jones RS, Ward JR (1963) Studies on adjuvant-induced polyarthritis in rats. II. Histogenesis of joint and visceral lesions. Arth Rheum 6: 23–35

    Article  CAS  Google Scholar 

  53. Pearson CM, Wood FD (1963) Studies of arthritis and other lesions induced by the injection of mycobacterial adjuvant. VII: Pathologic details of the arthritis and spondylitis. Am J Pathol 42: 73–95

    CAS  PubMed  Google Scholar 

  54. Muirden KD, Peace G (1969) Light and electron microscope studies in carragheenin, adjuvant, and tuberculin-induced arthritis. Ann Rheum Dis 28: 392–401

    Article  CAS  PubMed  Google Scholar 

  55. Battisto JR, Smith RN, Beckman K, Sternlicht M, Welles WL (1982) Susceptibility to adjuvant arthritis in DA and F344 rats. A dominant trait controlled by an autosomal gene locus linked to the major histocompatibility complex. Arth Rheum 25: 1194–1200

    Article  CAS  Google Scholar 

  56. Griffiths MM, Eichwald EJ, Martin JH, Smith CB, DeWitt CW (1981) Immunogenetic control of experimental type II collagen-induced arthritis. I. Susceptibility and resistance among inbred strains of rats. Arth Rheum 24: 781–789

    Article  CAS  Google Scholar 

  57. Anderle SK, Greenblatt JJ, Cromartie WJ, Clark R, Schwab JH (1979) Modulation of the susceptibility of inbred and outbred rats to arthritis induced by cell walls of group A streptococci. Infect Immun 25: 484–490

    CAS  PubMed  Google Scholar 

  58. Wilder RL (1988) Streptococcal cell-wall-induced arthritis in rats: an overview. Int J Tiss React 10: 1–5

    CAS  Google Scholar 

  59. Sternberg EM, Young III WS, Bernardini R, Calogero AE, Chrousos GP, Gold PW, Wilder RL (1989) A central nervous system defect in biosynthesis of corticotropinreleasing hormone is associated with susceptibility to streptococcal cell wall-induced arthritis in Lewis rats. Proc Natl Acad Sci USA 86: 4771–4775

    Article  CAS  PubMed  Google Scholar 

  60. Sternberg EM, Glowa JR, Smith MA, Calogero AE, Listwak SJ, Aksentijevich S, Chrousos GP, Wilder RL, Gold PW (1992) Corticotropin releasing hormone related behavioral and neuroendocrine responses in Lewis and Fischer rats. Brain Res 570: 54–60

    Article  CAS  PubMed  Google Scholar 

  61. Klareskog L, Wigzell H (1988) Immune reactions in the rheumatoid synovial tissue. In: JA Goodacre, WC Dick (eds): Immunopathogenetic mechanisms of arthritis. MTP Press Limited, Lancaster, 143–157

    Chapter  Google Scholar 

  62. Joosten I, Wauben MHM, Holewijn MC, Reske K, Pedersen LO, Roosenboom CFP, Hensen EJ, van Eden W, Buus S (1994) Direct binding of autoimmune-disease related T-cell epitopes to purified Lewis rat MHC class-II molecules. Int Immunol 6: 751–759

    Article  CAS  PubMed  Google Scholar 

  63. Stimpson SA, Schwab JH (1989) Chronic remittent erosive arthritis induced by bacterial peptidoglycan-polysaccharide structures. In: JY Chang, AJ Lewis (eds): Modern methods in pharmacology: pharmacological methods in the control of inflammation. Alan R. Liss, Inc., New York, 381–394

    Google Scholar 

  64. van den Broek MF, van Bruggen MC, Koopman JP, Hazenberg MP, van den Berg WB (1992) Gut flora induces and maintains resistance against streptococcal cell wall-induced arthritis in F344 rats. Clin Exp Immunol 88: 313–317

    Article  PubMed  Google Scholar 

  65. Kohashi O, Kuwata J, Umehara K, Uemura F, Takahashi T, Ozawa A (1979) Susceptibility to adjuvant-induced arthritis among germfree specific-pathogen-free, and conventional rats. Infect and Immun 26: 791–794

    CAS  Google Scholar 

  66. Wilder RL, Calandra GB, Garvin AJ, Wright KD, Hansen CT (1982) Strain and sex variation in the susceptibility to streptococcal cell wall-induced polyarthritis in the rat. Arth Rheum 25: 1064–1072

    Article  CAS  Google Scholar 

  67. Sternberg EM, Hill JM, Chrousos GP (1989) Inflammatory mediator-induced hypothalamic-pituitary-adrenal axis activation is defective in streptococcal cell wall arthritis susceptible Lewis rats. Proc Natl Acad Sci USA 86: 2374–2378

    Article  CAS  PubMed  Google Scholar 

  68. Allen JB, Blatter D, Calandra GB, Wilder RL (1983) Sex hormonal effects on the severity of streptococcal cell wall-induced polyarthritis in the rat. Arth Rheum 26: 560–563

    Article  CAS  Google Scholar 

  69. Shear HL, Roubinian JR, Gil P, Talal N (1981) Clearance of sensitized erythrocytes in NZB/NZW mice. Effects of castration and sex hormone treatment. Eur J Immunol 11: 776–780

    Article  CAS  PubMed  Google Scholar 

  70. Robinson R (1979) Rat: Rat taxonomy. In: PL Altman, DD Katz (eds): Inbred and genetically defined strains of laboratory animals. Part 1: Mouse and rat. Federation of American Societies for Experimental Biology, Bethesda, 233–350

    Google Scholar 

  71. Tobach E, Bloch H (1955) A study of the relationship between behavior and susceptibility to tuberculosis in rats and mice. Adv Tuberc Res 6: 62–89

    Google Scholar 

  72. Aksetijevich S, Whitfield HR, Young WS, Wilder RL, Chrousos GP, Gold PW, Sternberg EM (1992) Arthritis-susceptible Lewis rats fail to emerge from the stress hyporesponsive period. Dev Brain Res 65: 115–118

    Article  Google Scholar 

  73. Penning TD Talley JJ Bertenshaw SR Carter JS Collins PW Docter S Graneto MJ Lee LF Malecha J W Miyashiro JM, et al. (1997) Synthesis and biological evaluation of the 1,5diarylpyrazole class of cyclooxygenase-2 inhibitors: identification of 4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide (SC-58635, celecoxib). J Med Chem 40: 1347–1365

    Google Scholar 

  74. Schwartz J, Mukhopadhyay S, McBride K, Jones T, Adcock S, Sharp P, Dedges J, Grasing K et al. (1998) Antipyretic activity of a selective cyclooxygenase (COX)-2 inhibitor, MK-966. Am Soc Clin Pharmacol Ther 63: 167

    Google Scholar 

  75. Carlson RP, Datko LJ, Chang J, Nielsen ST, Lewis AJ (1984) The antiinflammatory profile of (5H-dibenzo[a,d]-cyclohepten-5-ylidene)acetic acid (WY-41,770), an agent possessing weak prostaglandin synthetase inhibitory activity that is devoid of gastric side-effects. Agents and Actions 14: 654–661

    Article  CAS  PubMed  Google Scholar 

  76. Inoue K, Fujisawa H, Montonaga A, Inoue Y, Kyoi T, Ueda F, Kimura K (1994) Anti-inflammatory effects of etodolac: comparison with other non-steroidal anti-inflammatory drugs. Biol Pharm Bull 17: 1577–1583

    Article  CAS  PubMed  Google Scholar 

  77. Mukherjee A, Hale VG, Borga O, Stein R (1996) Predictability of the clinical potency of NSAIDs from the preclinical pharmacodynamics in rats. Inflamm Res 45: 531–540

    Article  CAS  PubMed  Google Scholar 

  78. Liyanage SP, Currey HLF (1972) Failure of oral d-penicillamine to modify adjuvant arthritis or immune response in the rat. Ann Rheum Dis 31: 521

    Article  CAS  PubMed  Google Scholar 

  79. Yamamoto N, Sakai F, Yamazaki H, Kawai Y, Nakahara K, Okuhara M (1996) Effects of FR133605, a novel cytokine suppressive agent, on bone and cartilage destruction in adjuvant arthritic rats. J Rheum 23: 1778–1783

    CAS  PubMed  Google Scholar 

  80. 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-1-benzopyran-4-one. 1st communication: antiinflammatory, analgesic and other related properties. Arzneim Forsch 42: 935–944

    CAS  Google Scholar 

  81. Neuman RG, Wilson BD, Barkley M, Kimball ES, Weichman BM, Wood DD (1987) Inhibition of prostaglandin biosynthesis by etodolac. I. Selective activities in arthritis. Agents and Actions 21: 160–166

    Article  CAS  PubMed  Google Scholar 

  82. Calhoun W, Gilman SC, Datko LJ, Copenhaver TW, Carlson RP (1992) Interaction studies of tilomisole, aspirin, and naproxen in acute and chronic inflammation with assessment of gastrointestinal irritancy in the rat. Agents and Actions 36: 99–106

    Article  CAS  PubMed  Google Scholar 

  83. Ackerman NR, Rooks WH, Shott L, Genant H, Maloney P, West E (1979) Effects of naproxen on connective tissue changes in the adjuvant arthritic rat. Arth Rheum 22: 1365–1374

    Article  CAS  Google Scholar 

  84. Weichman BM (1989) Rat adjuvant arthritis: a model of chronic inflammation. In: JY Chang, AJ Lewis (eds): Pharmacological methods in the control of inflammation. Alan R. Liss, Inc., New York, 363–380

    Google Scholar 

  85. Lewis AJ, Carlson RP, Chang J, Gilman SC, Nielsen S, Rosenthale ME, Janssen FW, Ruelius HW (1983) The pharmacological profile of oxaprozin, an antiinflammatory and analgesic agent with low gastrointestinal toxicity. Curr Therap Res 34: 777–794

    CAS  Google Scholar 

  86. Swingle KF, Moore GI, Grant TJ (1976) 4-nitro-2-phenoxymethanesulfonanilide (R805): a chemically novel anti-inflammatory agent. Arch Int Pharmacodyn 221: 132–139

    Google Scholar 

  87. 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 Immunopharmacol 10: 717–728

    Article  CAS  PubMed  Google Scholar 

  88. Carlson RP, Hartman DA, Tomcheck 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

    CAS  PubMed  Google Scholar 

  89. Connolly KM, Stecher VJ, Danis E, Pruden DJ, LaBrie T (1988) Alteration of interleukin-1 activity and the acute phase response in adjuvant arthritic rats treated with disease modifying antirheumatic drugs. Agents and Actions 25: 94–105

    Article  CAS  PubMed  Google Scholar 

  90. Hara M, Sugawara S, Hirose S, Kondo H, Irimajiri S, Uchida S, Hashimoto H, Kashiwazaki S (1995) Immunological and therapeutical effects of FK506 on patients with rheumatoid arthritis. Inflamm Res 44: S248

    Article  Google Scholar 

  91. Carlson RP, Hartman DA, Ochalski SJ, Zimmerman JL, Glaser KB (1998) Sirolimus (Rapamycin, Rapamune) and combination therapy with cyclosporin A in the rat developing adjuvant arthritis model: correlation with blood levels and the effects of different oral formulations. Inflamm Res 47: 339–344

    Article  CAS  PubMed  Google Scholar 

  92. Bartlett RR, Schleyerback 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 Immunopharmac 7: 7–18

    Article  CAS  Google Scholar 

  93. Ohta Y, Fukuda S, Baba A, Nagai H, Tsukuda R, Sohda T, Makino H (1996) Immunomodulating and articular protecting activities of a new anti-rheumatic drug, TAK-603. Immunopharm 34: 17–26

    Article  CAS  Google Scholar 

  94. Badger AM, Bradbeer JN, Votta B, Lee JC, Adams JL, Griswold DE (1996) Pharmacological profile of SB 203580, a selective inhibitor of cytokine suppressive binding protein/p38 kinase, in animal models of arthritis, bone resorption, endotoxin shock and immune function. J Pharmacol Exp Therap 279: 1453–1461

    CAS  Google Scholar 

  95. Gouret C, Mocquet G, Raynaud G (1976) Use of Freund’s adjuvant arthritis test in anti-inflammatory drug screening in the rat: value of animal selection and preparation at the breeding center. Lab Animal Science 26: 281–287

    CAS  Google Scholar 

  96. Arrigoni-Martelli E, Bramm E (1975) Investigations on the influence of cyclophosphamide, gold sodium thiomalate and D-penicillamine on nystatin oedema and adjuvant arthritis. Agents and Actions 5: 264–267

    Article  CAS  Google Scholar 

  97. Dunn CJ, Prouteau M, Delahaye M, Purcell T, Branceni D (1984) Prolonged treatment with D-penicillamine effects on adjuvant arthritis in the rat. Agents and Actions 14: 269–273

    Article  CAS  PubMed  Google Scholar 

  98. Finkelstein AE, Ladizesky M, Borinsky R, Kohn E, Ginsburg I (1988) Antiarthritic synergism of combined oral and parenteral chrysotherapy. I. Studies in adjuvant-induced arthritis in rats. Inflammation 12: 373–382

    Article  CAS  PubMed  Google Scholar 

  99. Morris RE, Meiser BM, Wu J, Shorthouse R, Wang J (1991) Use of rapamycin for the suppression of alloimmune reactions in vivo: schedule dependence, tolerance induction, synergy with cyclosporine and FK-506, and effect on host-versus-graft and graft-versushost reactions. Transplant Proc 23: 521–524

    CAS  PubMed  Google Scholar 

  100. Billingham MEJ, Hicks CA, Carney SL (1990) Monoclonal antibodies and arthritis. Agents and Actions 29: 77–87

    Article  CAS  PubMed  Google Scholar 

  101. Yoshino S, Schlipkoter E, Kinne R, Hunig T, Emmrich F (1990) Suppression and prevention of adjuvant arthritis in rats by a monoclonal antibody to the aß T cell receptor. Eur J Immunol 20: 2805–2808

    Article  CAS  PubMed  Google Scholar 

  102. Issekutz AC, Meager A, Otterness I, Issekutz TB (1994) The role of tumour necrosis factor-alpha and IL-1 in polymorphonuclear leucocyte and T lymphocyte recruitment to joint inflammation in adjuvant arthritis. Clin Exp Immunol 97: 26–32

    Article  CAS  PubMed  Google Scholar 

  103. Fergusson KM, Osawa H, Diamanstein T, Oronsky AL, Kerwar SS (1988) Treatment with an anti-interleukin 2 receptor antibody protects rats from passive but not adjuvant arthritis. Int J Immunother IV: 29–33

    Google Scholar 

  104. Issekutz AC, Ayer L, Miyasaka M, Issekutz TB (1996) Treatment of established adjuvant arthritis in rats with monoclonal antibody to CD18 and very late activation antigen-4 integrins suppresses neutrophil and T-lymphocyte migration to the joints and improves clinical disease. Immunology 88: 569–576

    Article  CAS  PubMed  Google Scholar 

  105. Seiffge D (1996) Protective effects of monoclonal antibody to VLA-4 on leukocyte adhesion and course of disease in adjuvant arthritis in rats. J Rheum 23: 2086–2091

    CAS  PubMed  Google Scholar 

  106. Iigo Y, Takashi T, Tamatani T, Miyasaka M, Higashida T, Yagita H, Okumuru K, Tsukada W (1991) ICAM-1-dependent pathway is critically involved in the pathogenesis of adjuvant arthritis in rats. J Immunol 147: 4167–4171

    CAS  PubMed  Google Scholar 

  107. Walter UM, Issekutz AC (1997) The role of E- and P-selectin in neutrophil and monocyte migration in adjuvant-induced arthritis in the rat. Eur J Immunol 27: 1498–1505

    Article  CAS  PubMed  Google Scholar 

  108. Santos LL, Morand EF, Hutchinson P, Boyce NW, Holdsworth SR (1997) Anti-neutrophil monoclonal antibody therapy inhibits the development of adjuvant arthritis. Clin Exp Immunol 107: 248–253

    Article  CAS  PubMed  Google Scholar 

  109. Hoffmann JC, Herklotz C, Zeidler H, Bayer B, Rosenthal H, Westermann J (1997) Initiation and perpetuation of rat adjuvant arthritis is inhibited by the anti-CD2 monoclonal antibody (mAb) OX34. Ann Rheum Dis 56: 716–722

    Google Scholar 

  110. Jacob CO, Holoshitz J, van der Meide P, Strober S, McDevitt HO (1989) Heterogeneous effects of IFN-gamma in adjuvant arthritis. J Immunol 142: 1500–1505

    CAS  PubMed  Google Scholar 

  111. Nakajima H, Takamori H, Hiyama Y, Tsukada W (1991) The effect of treatment with recombinant gamma-interferon on adjuvant-induced arthritis in rats. Agents and Actions 34: 63–65

    Article  CAS  PubMed  Google Scholar 

  112. Feige U, Schulmeister A, Mollenhauer J, Brune K, Bang H (1994) A constitutive 65kDa chondrocyte protein as a target antigen in adjuvant arthritis in Lewis rats. Autoimmunity 17: 233–239

    Article  CAS  PubMed  Google Scholar 

  113. Zhang ZJ, Lee CSY, Lider O, Weiner HL (1990) Suppression of adjuvant arthritis in Lewis rats by oral administration of type II collagen. J Immunol 145: 2489–2493

    CAS  PubMed  Google Scholar 

  114. Halloran MM, Szekanecz Z, Barquin N, Haines GK, Koch AE (1996) Cellular adhesion molecules in rat adjuvant arthritis. Arth Rheum 39: 810–819

    Article  CAS  Google Scholar 

  115. Clegg DO, Dietz F, Duffy J, Willkens RF, Hurd E, Germain BF, Wall B, Wallace DJ, Bell CL, Sleckman J (1997) Safety and efficacy of hydroxychloroquine as maintenance therapy for rheumatoid arthritis after combination therapy with methotrexate and hydroxychloroquine. J Rheum 24: 1896–1902

    CAS  PubMed  Google Scholar 

  116. Murray KM, Dahl SL (1997) Recombinant human tumor necrosis factor receptor (p75) Fc fusion protein (TNFR:Fc) in rheumatoid arthritis. Ann Pharmacother 31: 1335–1338

    CAS  PubMed  Google Scholar 

  117. Brower V (1997) Enbrel’s phase III reinforces prospects in RA. Nat Biotechnol 15: 1240

    Article  CAS  PubMed  Google Scholar 

  118. Niederer RR (1984) Topical anti-inflammatory activity of suprofen in the adjuvant arthritic rat. Bull Tech/Gattefosse 77: 43–45

    CAS  Google Scholar 

  119. Hiramatsu Y, Akita S, Salamin PA, Maier R (1990) Assessment of topical non-steroidal anti-inflammatory drugs in animal models. Arzneiur Forsch 40: 1117–1124

    CAS  Google Scholar 

  120. Lopez-Guerrero JA, Lopez-Bote JP, Ortiz MA, Gupta RS, Paez E, Bernabeu C (1993) Modulation of adjuvant arthritis in Lewis rats by recombinant vaccinia virus expressing the human 60-kilodalton heat shock protein. Infect Immun 61: 4225–4231

    CAS  PubMed  Google Scholar 

  121. Makarov SS, Olsen JC, Johnston WN, Schwab JH, Anderle SK, Brown RR, Haskill JS (1995) Retrovirus mediated in vivo gene transfer to synovium in bacterial cell wall-induced arthritis in rats. Gene Ther 2: 424–428

    CAS  PubMed  Google Scholar 

  122. Wahl SM, Allen JB, Ohura K, Chenoweth DE, Hand AR (1991) IFN-gamma inhibits inflammatory cell recruitment and the evolution of bacterial cell wall-induced arthritis. J Immunol 146: 95–100

    CAS  PubMed  Google Scholar 

  123. Sano H, Hla T, Maier JAM, Crofford LJ, Case JP, Maciag T, Wilder RL (1992) in vivo cyclooxygenase experession in synovial tissues of patients with rheumatoid arthritis and osteoarthritis and rats with adjuvant and streptococcal cell wall arthritis. J Clin Invest 89: 97–108

    Google Scholar 

  124. Yocum DE, Allen JB, Wahl SM, Calandra GB, Wilder RL (1986) Inhibition by cyclosporin A of streptococcal cell wall-induced arthritis and hepatic granulomas in rats. Arth Rheum 29: 262–273

    Article  CAS  Google Scholar 

  125. van den Broek MF, van de Langerigt LGM, van Bruggen MCJ, Billinghan MEJ, van den Berg WB (1992) Treatment of rats with monoclonal anti-CD4 induces long-term resistance to streptococcal cell wall-induced arthritis. Eur J Immunol 22: 57–61

    Article  PubMed  Google Scholar 

  126. Yoshino S, Cleland L, Mayerhofer G, Brown R, Schwab J (1991) Prevention of chronic erosive streptococcal cell wall-induced arthritis in rats by treatment with monoclonal antibody against the T cell antigen receptor a,ß. J Immunol 146: 1487–1489

    Google Scholar 

  127. Schimmer RC, Schrier DJ, Flory CM, Dykens J, Tung DKL, Jacobson PB, Friedl HP, Conroy MC, Schimmer BB, Ward PA (1997) Streptococcal cell wall-induced arthritis. Requirements for neutrophils, P-selectin, intercellular adhesion molecule-1, and macrophage-inflammatory protein-2. J Immunol 159: 4103–4108

    Google Scholar 

  128. Schwab JH, Anderle SK, Brown RR, Dalldorf FG, Thompson RC (1991) Pro-and anti-inflammatory roles of interleukin-1 in recurrence of bacterial cell wall-induced arthritis in rats. Infect Immun 59: 4436–4442

    CAS  PubMed  Google Scholar 

  129. Schrier DJ, Schimmer RC, Flory CM, Tung DK, Ward PA (1998) Role of chemokines and cytokines in a reactivation model of arthritis in rats induced by injection with streptococcal cell walls. J Leuk Biol 63: 359–363

    CAS  Google Scholar 

  130. Wahl SM, Allen JB, Costa GL, Wong HL, Dasch JR (1993) Reversal of acute and chronic synovial inflammation by anti-transforming growth factor beta. J Exp Med 177: 225–230

    Article  CAS  PubMed  Google Scholar 

  131. Schimmer RC Schrier DJ Flory CM Laemont KD Tung D Metz AL Friedl HP Conroy MC Warren JS Beck B, et al. (1998) Streptococcal cell wall-induced arthritis: requirements for IL-4, IL-10, IFN-y, and monocyte chemoattractant protein-1. J Immunol 160: 1466–1471

    Google Scholar 

  132. van den Broek MF, Hogervorst EJM, van Bruggen MCJ, van Eden W, van der Zee R, van den Berg WB (1989) Protection against streptococcal cell wall-induced arthritis by pretreatment with the 65-kD mycobacterial heat shock protein. J Exp Med 170: 449–466

    Google Scholar 

  133. Brandes M, Allen JB, Ogawa Y, Wahl SM (1991) Transforming growth factor beta 1 suppresses acute and chronic arthritis in experimental animals. J Clin Invest 87: 11081113

    Google Scholar 

  134. Allen JB, Wong HL, Costa GL, Bienkowski MJ, Wahl SM (1993) Suppression of monocyte function and differential regulation of IL-1 and IL-1ra by IL-4 contribute to a resolution of experimental arthritis. J Immunol 151: 4344–4351

    CAS  PubMed  Google Scholar 

  135. Allen JB, Bansal GP, Feldman GM, Hand AO, Wahl LM, Wahl SM (1991) Suppression of bacterial cell wall-induced polyarthritis by recombinant gamma interferon. Cytokine 3: 98–106

    Article  CAS  PubMed  Google Scholar 

  136. Jacobson PB, Morgan S, Wilcox D, Carlson R, Harris R, Nuss M (1998) A new spin on an old model: magnetic resonance imaging of the adjuvant arthritis rat. in vivo evaluation of disease progression by MRI with respect to standard inflammatory parameters and histopathology. Arth Rheum; submitted

    Google Scholar 

  137. Jones RS, Ward JR (1963) Studies on adjuvant-induced polyarthritis in rats. II. Histogenesis of joint and visceral lesions. Arth Rheum 6: 23–35

    Article  CAS  Google Scholar 

  138. Weichman BM, Chau TT, Rona G (1987) Histopathologic evaluation of the effects of etodolac in established adjuvant arthritis in rats: evidence for reversal of joint damage. Arth Rheum 30: 466–470.

    Article  CAS  Google Scholar 

  139. Mohr W, Wild A, Wolf HP (1981) Role of polymorphs in inflammatory cartilage destruction in adjuvant arthritis in rats. Ann Rheum Dis 40: 171–176

    Article  CAS  PubMed  Google Scholar 

  140. Wilder RL, Case JP, Crofford LJ, Kumkumian GK, Lafyatis R, Remmers EF, Sano H, Sternberg EM, Yocum DE (1991) Endothelial cells and the pathogenesis of rheumatoid arthritis in humans and streptococcal cell wall arthritis in Lewis rats. J Cell Biochem 45: 162–166

    Google Scholar 

  141. Schrier DJ, Flory CM, Finkel M, Kuchera SL, Lesch ME, Jacobson PB (1996) The effects of the phospholipase A2 inhibitor, manoalide, on cartilage degradation, stromelysin expression, and synovial fluid cell count induced by intraarticular injection of human recombinant interleukin-1 alpha in the rabbit. Arth Rheum 39: 1292–1299

    Article  CAS  Google Scholar 

  142. Sano H, Forough R, Maier JA, Case JP, Jackson A, Engleka K, Maciag T, Wilder RL (1990) Detection of high levels of heparin binding growth factor-1 (acidic fibroblast growth factor) in inflammatory arthritic joints. J Cell Biol 110: 1417–1426

    Article  CAS  PubMed  Google Scholar 

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Carlson, R.P., Jacobson, P.B. (1999). Comparison of adjuvant and streptococcal cell wall-induced arthritis in the rat. In: Morgan, D.W., Marshall, L.A. (eds) In Vivo Models of Inflammation. Progress in Inflammation Research. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-7775-6_1

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