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The Role of Exogenous Stimulation in Pathogenesis of Autoimmune Diseases

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Autoimmune Reactions

Part of the book series: Contemporary Immunology ((CONTIM))

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Abstract

A properly operating immune system enables the body to maintain a healthy status quo by distinguishing between the antigens associated with the organism itself, which are allowed to persist, and the antigens borne by foreign molecules, which are disposed. Burnet (1). proposed that the ability of immune system to distinguish “self and nonself ‘antigens results from the elimination of self-reactive lymphocytes during ontogenic development. This concept is supported by recent data originating from studies carried out in transgenic mice demonstrating that self-reactive T- and B- lymphocytes are deleted from the repertoire. In the thymus, a process known as negative selection appears to result in deletion of T-cells bearing receptors with high affinity for self-antigens (2,3). In the fetal liver and bone marrow, a similar process deletes the emerging B-cells bearing an Ig receptor specific for cellular antigens (4).

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References

  1. Burnett M. (1959) The Clonal Selection Theory of Acquired Immunity, Vanderbilt University Press, Nashville, TN.

    Google Scholar 

  2. Jacobs, H., von Boehmer, H., Melief, C. J., and Berns, A. (1990) Mutations in the major histocompatibility complex class I antigen presenting groove affect both negative positive selection of T cells. Eur. J. Immunol. 20, 2333–2337.

    Article  PubMed  CAS  Google Scholar 

  3. Hogguist, K. A., Jameson, S. C., Heath, W. R., Howard, J. L., Bevan, M. J., and Carbone, F. R. (1994) T cell receptor antagonist peptides induce positive selection. Cell 76, 229, 230.

    Article  Google Scholar 

  4. Hartly, S. B., Croslic, R., Brink, R., Kantor, A. B., Basten, A., and Goodnow, C. C. (1991) Elimination from peripheral lymphoid tissues of self-reactive B lymphocytes recognizing membrane-bound antigens. Nature 353, 765–769.

    Article  Google Scholar 

  5. Welch, M. J., Fong, S., Vaugham, J. H., and Carson, D. A. (1983) Increased frequency of rheumatoid factor precursor B lymphocytes after immunization of normal adults with tetanus toxoid. Clin. Exp. Immunol. 51, 299.

    PubMed  CAS  Google Scholar 

  6. Inman, R. D., Hodge, M., and Johnston, M. E. A. (1986) Arthritis, vasculitis and cryoglobulinemia associated with relapsing hepatitis A virus infection. Ann. Intern. Med. 105, 700–703.

    PubMed  CAS  Google Scholar 

  7. Czaja, A. J., Carpenter, H. A., and Santrach, P. J. (1993) Evidence against hepatitis viruses as important causes of severe autoimmune hepatitis in the United States. J. Hepatol. 18, 342–352.

    Article  PubMed  CAS  Google Scholar 

  8. Munke, H. F., Stockmann, F., and Ramdori, G. (1995) Possible association between Bechet’s syndrome and chronic hepatitis C virus infection. N. Engl. J. Med. 332, 400–401.

    Article  PubMed  CAS  Google Scholar 

  9. Anonymous. (1988) Guillian—Barre syndrome. Lancet 2, 659–661.

    Google Scholar 

  10. Hart, I. K. and Kennedy, P. G. E. (1988) Guillain—Barre syndrome associated with cytomegalovirus infection. Quart. J. Med. 253, 425–430.

    Google Scholar 

  11. Marchiili, B. Dolcher, M. P., and Sabbatini, A. (1994) Immune response to different sequences of the EBNAI molecule in Epstein-Barr virus-related disorders and in autoimmune diseases. J. Autoimmun. 7, 179–191.

    Article  Google Scholar 

  12. Tosato, G., Steinber, A. D., and Blaesc, R. M. (1981) Defective EBV-specific suppressor T-cell function in rheumatoid arthritis. N. Engl. J. Med. 305, 1238–1243.

    Article  PubMed  CAS  Google Scholar 

  13. Silverman, S. L. and Schmacher, H. R. (1981) Antibodies to Epstein-Barr viral antigens in early rheumatoid arthritis. Arthritis Rheum. 24, 1465–1468.

    Article  Google Scholar 

  14. Tosato, G., Steinberg, D., and Yarchoan R. (1984) Abnormally elevated frequency of Epstein-Barr virus-infected B cells in the blood of patients with rheumatoid arthritis. J. Clin. Invest. 73, 1789–1795.

    Article  PubMed  CAS  Google Scholar 

  15. Roudier, J. G., Rhodes, J., Petersen, F., et. al. (1988) The Epstein-Barr virus glyco-protein gp110, a molecular between HLA DR4, HLA DR1 and rheumatoid arthritis. Scand. J. Immunol. 27, 367–371.

    Article  PubMed  CAS  Google Scholar 

  16. Wilder, R. L. (1994) Hypothesis for retorviral causation of rheumatoid arthritis. Curr. Opin. Rheumatol. 6, 295–299.

    Article  PubMed  CAS  Google Scholar 

  17. Baranski, B., Armstrong, G., and Truman, J. T. (1988) Epstein-Barr virus in the bone marrow of patients with aplastic anemia. Ann. Intern. Med. 109, 695–704.

    PubMed  CAS  Google Scholar 

  18. Whittingham, S. M., McNeilage, J., and Mackay, I. R. (1985) Primary Sjogren’s syndrome after infectious mononucleosis. Ann. Intern. Med. 102, 490–493.

    PubMed  CAS  Google Scholar 

  19. Fox, R. I., Luppi, M., Kang, H. I., and Pisa, P. (1991) Reactivation of Epstein-Barr virus in Sjögren’s syndrome. Springer Semin. Immunopathol. 13, 217–231.

    Article  PubMed  CAS  Google Scholar 

  20. Deacon, I. M., Shattles, W. G., and Mathews, J. B. (1992) Frequency of EBV DNA detection in Sjögren’s syndrome. Am. J. Med. 92, 453–454.

    Article  PubMed  CAS  Google Scholar 

  21. Fox, R. I., Luppi, M., and Pisa, P. (1992) Potential role of EBV in Sjögren’s syndrome and rheumatoid arthritis. J. Rheumatol. 19, 18–24.

    Google Scholar 

  22. Baboonian, C., Benables, P. J. W., and Maini, R. N. (1990) Antibodies to human herpesvirus-6 in Sjogren’s syndrome. Arthritis Rheum. 33, 1749,1750.

    Article  PubMed  CAS  Google Scholar 

  23. Huber, S. A. and Lodge, P. A. (1984) Coxsackie B-3 myocarditis in BALB/c mice. Am. J. Pathol. 116, 21–29.

    PubMed  CAS  Google Scholar 

  24. Wolfgram, L. J., Beisel, K. W., and Rose, N. R. (1985) Heart-specific auto-antibodies following murine coxsackievirus B3 myocarditis. J. Exp. Med. 161, 1112–1121.

    Article  PubMed  CAS  Google Scholar 

  25. Beisel, K. W., Srinivasappa, J., and Prabhakar, B. S. (1991) Identification of a putative shared epitope between Coxsackie virus B4 and alpha cardiac myosin heavy chain. Clin. Exp. Immunol. 86, 49–55.

    Article  PubMed  CAS  Google Scholar 

  26. Neumann, D. A., Rose, N. R., and Ansari, A. A. (1994) Induction of multiple heart autoantibodies in mice with coxsackievirus B3 and cardiac myosin-induced autoimmune myocarditis. J. Immunol. 152, 343–350.

    PubMed  CAS  Google Scholar 

  27. Reid, D. M., Reid, T. M., and Brown, T. (1985) Human parvovirus-associated arthritis: a clinical and laboratory description. Lancet 1, 422–425.

    Article  PubMed  CAS  Google Scholar 

  28. Corman, L. C. and Dolson, D. J. (1992) Polyarteritis nodosa and parvovirus B19 infection. Lancet 339, 491.

    Article  PubMed  CAS  Google Scholar 

  29. Secry, J. P. (1990) The link between viral infection and autoimmunity. Rev. Infect. Dis. 12, 1202.

    Article  Google Scholar 

  30. Bodansky, H. J., Liitlewood, J. M., Bottazzo, G. F. Dean, B. M., and Hambling, M. H. (1984) Which virus causes the initial islet lesion in type 1 diabetes? Lancet 1, 401, 4

    Article  PubMed  CAS  Google Scholar 

  31. Oldstone, M. B., Nerenberg, M., and Southern, P. (1991) Virus infection triggers insulin-dependent diabetes mellitus in a transgenic model: role of anti-self (virus) immune response. Cell 65, 319–331.

    Article  PubMed  CAS  Google Scholar 

  32. Taniguchi, A., Takenaka, Y., Noda, Y., Ueno, Y., Shichikawa, K., Sato, K., et al. (1988) Adult T cell leukemia presenting with proliferative synovitis. Arthritis Rheum. 31, 1076, 1077.

    Article  PubMed  CAS  Google Scholar 

  33. Banki, K., Maceda, J., Hurley, E., Ablonczy, E., Mattson, D. H., Szegedy, L., et al. (1992) HTLV-related endogenous sequence, HRES-1 encodes a 28KD protein: a possible autoantigen for HTLV-1 gag reactive autoantibodies. Proc. Natl. Acad. Sci. USA 89, 1939–1943.

    Article  PubMed  CAS  Google Scholar 

  34. Matsumoto, Y., Hibino, N., Kamimura, M., and Nishioka, K. (1990) Jpn. J. Int. Med. 79, 1589–1590.

    Article  CAS  Google Scholar 

  35. Sagawa, K., Moochizuki, M., Masuoka, K., Katagiri, K., Katayama, T., Maeda, T., et al. (1995) Immunopathological mechanisms of HTLV-1 uveilts. J. Clin. Invest. 95, 852–858.

    Article  PubMed  CAS  Google Scholar 

  36. Nemazee, D. A. and Sato, V. L. (1983) Induction of rheumatoid antibody in the mouse: regulated production of autoantibody in the secondary humoral response. J. Exp. Med. 158, 545.

    Article  Google Scholar 

  37. Manheimer, A. and Bona, C. (1985) Anti-immunoglobulin antibodies VI. Age-dependent isotype and autoimmunoglobulin variation during secondary immune response in 129 mice. Mech. Ageing Dev. 30, 187–199.

    Article  PubMed  CAS  Google Scholar 

  38. Bailey, N. C., Fidanza, V., Mayer, R., Mazza, G., Fougereau, M., and Bona, C. (1989) Activation of clones producing self-reactive antibodies by foreign antigen and antiidiotype antibody carrying the internal image of the antigen. J. Clin. Invest. 84, 744–756.

    Article  PubMed  CAS  Google Scholar 

  39. Coutelier, J. P., van der Logt, J. J. M., Hessen, F. W. A., Warmier, G., and van Snick, J. (1986) Rheumatoid factor production in 129/Sv mice: involvement of an intestinal infectious agent. J. Immunol. 137, 337.

    PubMed  CAS  Google Scholar 

  40. Theophilopoulos, A. N., Balderas, R. S., Hand, L., and Dixon, F. J. (1983) Monoclonal IgM Rheumatoid factors derived from arthritic MRL/MP-1pr/1pr mice. J. Exp. Med. 158, 901.

    Article  Google Scholar 

  41. Manheimer, A. J., Victor-Kobrin, C., Stein, K. E., and Bona, C. A. (1984) Antiimmunoglobulin antibodies V. Age-dependent variation of clones stimulated by polysaccharide T1-2 antigens in 129 and MRL mice spontaneously producing anti-γ globulin antibodies. J. Immunol. 133, 562.

    PubMed  CAS  Google Scholar 

  42. Cohen, A. D. and Shoenfeld, Y. (1995) The viral autoimmunity relationship. Viral Immunol. 8, 1–9.

    Article  PubMed  CAS  Google Scholar 

  43. Newmark, P. (1995) Multiple sclerosis and viruses. Nature 318, 101.

    Google Scholar 

  44. Futo, F., Saag, K. G., and Scharosch, L. L. (1993) Parvovirus B19-specific DVH in bone marrow from B19 arthropathy patients: evidence for B19 virus persistence. J. Infect. Dis. 167, 744–748.

    Article  Google Scholar 

  45. Sasaki, T., Murai, C., Muryoi, T. Takahashi, Y., Munakata, Y., Sugamura, M., et al. (1995) Persistent infection of human parvovirus B19 in a normal subject. Lancet 346, 851.

    Article  PubMed  CAS  Google Scholar 

  46. Murai, C., Munakata, Y., Takahashi, Y., Ishii, T., Muryoi, T., Abe, K., et al. Rheumatoid arthritis after humanparvovirus B19 infection (submitted).

    Google Scholar 

  47. Hasunuma, T., Sumida, T., and Nishioka, K. (1997) Human T cell leukemia virus type 1 and rheumatoid arthritis. Int. Rev. Immunol., in press.

    Google Scholar 

  48. Izui, S., Eisenberg, R. A., and Dixon, F. J. (1979) IgM rheumatoid factors in mice injected with bacterial lipopolysaccharides. J. Immunol. 122, 2096.

    PubMed  CAS  Google Scholar 

  49. Theophilpoulos, A. (1995) The basis of autoimmunity. Immunol. Today 16, 90–98.

    Google Scholar 

  50. Murakami, M., Tsubata, T., Okamoto, M., Shimizu, A., Kumagai, S., Imura, H., et al. (1992) Antigen-induced apoptotic death of Ly-1 B cells that are responsible for autoimmune disease in transgenic mice. Nature 357, 77–80.

    Article  PubMed  CAS  Google Scholar 

  51. Zang, G.-X., Ma, C.-G., Xiao, B.-G., Bakhiet, M., Link, H. and Olson, T. (1995) Depletion of CD8+ T cells suppresses the development of myasthenia gravis in Lewis rats. Eur. J. Immunol. 25, 1191–1198.

    Article  Google Scholar 

  52. Moffatt, S., Tanaka, N., Tada, K., Nose, M., Nakamura, M., Muraoka, O., et al. (1996) A cytotoxic non structural protein, NS1, of human parvovirus B19. J. Virol 70, 8485–8491.

    PubMed  CAS  Google Scholar 

  53. Hirano, T. T., Matsuda, M., Turner, N., Miyasaka, G., Buchan, B., Tang, K., et al. (1988) Excessive production of interleukin 6/B cell stimulatory factor-2 in rheumatoid arthritis. Eur. J. Immunol. 18, 1797–1801.

    Article  PubMed  CAS  Google Scholar 

  54. Hirano, T., Akira, S., Taga, T., and Kishimoto, T. (1990) Biological and clinical aspects of interleukin 6. Immunol. Today 11, 443–449.

    CAS  Google Scholar 

  55. Jorgensen, C., Angel, J., and Fournier, C. (1991) Regulation of synovial cell proliferation and prostaglandin E2 production by combined action of cytokines. Eur. Cytokine Netw. 2, 207–215.

    PubMed  CAS  Google Scholar 

  56. Mihara, M., Moriya, Y., Kishimoto, T., and Ohsugi, Y. (1995) Interleukin-6 (IL-6) induces the proliferation of synovial fibroblastic cells in the presence of soluble IL-6 receptor. Br. J. Rheum. 34, 321–325.

    Article  CAS  Google Scholar 

  57. Nakajima, T., Aono, H., Hasunuma, T., Yamamoto, K., Maruyama, I., Nosaka, T., et al. (1993) Overgrowth of human synovial cells driven by HTLV-1 virus Tax gene. J. Clin. Invest. 92, 186–193.

    Article  PubMed  CAS  Google Scholar 

  58. Iwakura, Y., Saijo, S., Kioka, Y., Nakayama-Yamada, J., Itagaki, K., Tosu, M., et al. (1995) Autoimmunity induction by HTLV-1 virus in transgene mice that develop chronic flammatory arthropathy resembling rheumatoid arthritis in humans. J. Immunol. 155, 1588–1598.

    PubMed  CAS  Google Scholar 

  59. Gamow, G., Sercarz, E. E., and Benichou, G. (1991) The dominant self and the cryptic self: shaping the autoreactive T-cell repertoire. Immunol. Today 12, 193–195.

    Google Scholar 

  60. Witebsky, E., Rose, N. R., Terplan, K., Paine, J. R., and Egan, R. W. (1957) Chronic thyroiditis and autoimmunization. J. Am. Med. Assoc. 164, 1439–1447.

    Article  PubMed  CAS  Google Scholar 

  61. Kaplan, M. H. and Sevc, K. H. (1964) Immunologic relations of streptococcal and tissue antigens. III. Presence in human sera of streptococcal antibody crossreactive with heart tissue. Association with streptococcal infection, rheumatic fever and glomerulonephritis. J. Exp. Med. 119, 651–666.

    Article  PubMed  CAS  Google Scholar 

  62. Zabriskie, J. B., Hsu, K. C., and Seegal, B. C. (1970) Heart-reactive antibody associated with rheumatic fever: characterization and diagnostic significance. Clin. Exp. Immunol. 7, 147–159.

    PubMed  CAS  Google Scholar 

  63. Krisher, K. and Cunningham, M. W. (1985) Myosin: a link between streptococci and heart. Science 227, 413–415.

    Article  PubMed  CAS  Google Scholar 

  64. Cunningham, M. W., Hall, N. K., and Krisher, K. K. (1986) A study of anti-group A streptococcal monoclonal antibodies cross-reactive with myosin. J. Immunol. 136, 293–298.

    PubMed  CAS  Google Scholar 

  65. Dale, J. B. and Beachey, E. H. (1986) Epitopes of streptococcal M proteins shared with cardiac myosin. J. Exp. Med. 162, 583–591.

    Article  Google Scholar 

  66. Husby, G., van de Rijn, I., Zabriskie, J. B., Abdin, Z. H. and Williams, R. C., Jr. (1976) Antibodies reacting with cytoplasm of subthalamic and caudate nuclei neutrons in chorea and acute rheumatic fever. J. Exp. Med. 144, 1094–1110.

    Article  PubMed  CAS  Google Scholar 

  67. Fillit, H., Damle, S. P., and Gregory, J. D. (1985) Sera from patients with poststreptococcal glomerulonephritis contain antibodies to glomerular heparan sulfate proteoglycan J. Exp. Med. 161, 277–2

    Article  PubMed  CAS  Google Scholar 

  68. Fujinami, R. S. and Oldstone, M. B. A. (1985) Amino acid homology between the encephalitogenic site of myelin basic protein and virus: mechanism for autoimmunity. Science 230, 1043–1045.

    Article  PubMed  CAS  Google Scholar 

  69. Jahnke, U., Fischer, E. H., and Alvord, E. C., Jr. (1985) Sequence homology between certain viral proteins and proteins related to encephalomyelitis and neuritis. Science 229, 282–284.

    Article  PubMed  CAS  Google Scholar 

  70. Johnson, R. T., Griffin, D. E., Hirsch, R. L., Wolinsky, J. W., Roedenbeck, S., Lindo de Sorian, I., et al. (1984) Measles encephalomyelitis: clinical and immunological studies. N. Engl. J. Med. 310, 137–141.

    Article  PubMed  CAS  Google Scholar 

  71. Johnson, R. I. and Griffin, E. D. (1996) Virus-induced autoimmune demyelinating disease of the central nervous system, in Concepts in Viral Pathogenesis, Vol. II (Notkins, A.L. and Oldstone, M.B.A., eds), Springer-Verlag, New York, pp. 203–209.

    Google Scholar 

  72. Oldstone, M. B. A. (1987) Molecular mimicry and autoimmune disease. Cell 50, 819–820.

    Article  PubMed  CAS  Google Scholar 

  73. Dyrberg, T. and Oldstone, M. B. A. (1986) Peptides as probes to study molecular mimicry and virus induced autoimmunity. Curr. Top. Microbiol. Immunol. 130, 25–37.

    Article  PubMed  CAS  Google Scholar 

  74. Singh, V. K., Yamaki, K., Abe, T., and Shinohara, T. (1989) Molecular mimicry between uveitopathogenic site of retinal S-antigen and Escherichia coli protein: induction of experimental autoimmune Uveitis and lymphocyte Cross-reaction. Cell. Immunol. 122, 262–273.

    Article  PubMed  Google Scholar 

  75. Maul, G. G., Jimenez, S. A., Riggs, E., and Ziemnicka-Kotula, D. (1989) Determination of an epitope of the diffuse systemic sclerosis marker antigen DNA topoisomerase I: sequence similarity with retroviral p30gag protein suggest a possible cause for autoimmunity in systemic sclerosis. Proc. Natl. Acad. Sci. USA 86, 8492–8496.

    Article  PubMed  CAS  Google Scholar 

  76. Muryoi, T., Kasturi, K., Kafina, M. J., Cram, D. S., Harrison, L. C., Sasaki, T., et al. (1993) Antitoposiomerase I monoclonal autoantibodies from scleroderma patients and tight skin mouse interact with similar epitopes. J. Exp. Med. 175, 1103–1109.

    Article  Google Scholar 

  77. Kasturi, K., Hatakeyama, A., Spiera, H., and Bona, C. (1985) Antifibrillarin autoantibodies present in systemic sclerosis and other connective tissue diseases interact with similar epitopes. J. Exp. Med. 181, 1027–1036.

    Article  Google Scholar 

  78. Douvas, A. and Sobelman, S. (1991) Multiple overlapping homologies between two rheumatoid antigens and immunosuppressive viruses. Proc. Natl. Acad. Sci. USA 88, 6328–6332.

    Article  PubMed  CAS  Google Scholar 

  79. Hemachudha, T., Griffin, D. E., and Giffels, J. J. (1987) Myelin basic protein as an encephalitogen in encephalomyelitis and polyneuritis following rabies vaccination. N. Engl. J. Med. 316, 369–374.

    Article  PubMed  CAS  Google Scholar 

  80. Bona, C. (1991) Postulates defining pathogenic autoantibodies and T-cells. Autoimmunity 10, 169–172.

    Article  PubMed  CAS  Google Scholar 

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Bona, C., Murai, C., Sasaki, T. (1999). The Role of Exogenous Stimulation in Pathogenesis of Autoimmune Diseases. In: Paul, S. (eds) Autoimmune Reactions. Contemporary Immunology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-4612-1610-0_10

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  • DOI: https://doi.org/10.1007/978-1-4612-1610-0_10

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