T-Cell Receptors and Collagen Induced Arthritis in H-2^R Mice

References

• Stuart J M, Townes A S, Kang A H. Collagen autoimmune arthritis. Ann Rev Immunol 1984; 2: 199–218
   PubMed Web of Science ®Google Scholar
• Holmdahl R, Andersson M, Goldschmidt T J, Gustafsson K, Jansson L, Mo J A. Type II collagen autoimmunity in animals and provocations leading to arthritis. Immunol Rev 1990; 118: 193–232
   PubMed Web of Science ®Google Scholar
• Seki N, Sudo Y, Yoshioka T, Sugihara S, Fujitsu T, Sakurna S, Ogawa T, Hamaoka T, Senoh H, Fijiwara H. Type II collagen-induced murine arthritis. I. Induction and perpetuation of arthritis require synergy between humoral and cell-mediated immunity. J Immunol 1988; 140: 1477–1484
   PubMed Web of Science ®Google Scholar
• Wooley P H, Chapdelaine J M. Immunogenetics of collagen-induced arthritis. CRC Crit Rev Immunol 1987; 8: 1–22
   Google Scholar
• David C S. Genes for MHC. TCR, and MIS determine susceptibility to collagen-induced arthritis. APMIS 1990; 98: 575–584
   PubMed Web of Science ®Google Scholar
• Wooley P H, Luthra H S, La Fuse W P, Huse A, Stuart J M, David C S. Type II collagen-induced arthritis in mice. II. Suppression of arthritis by using monoclonal and polyclonal anti-Ia antisera. J Immunol 1985; 134: 2366–2374
   PubMed Web of Science ®Google Scholar
• Gustafsson K, Karlsson M, Andersson L, Holmdahl R. Structures on the I-A molecule predisposing for susceptibility to type II collagen-induced autoimmune arthritis. Eur J Immunol 1990; 20: 2127–2131
   PubMed Web of Science ®Google Scholar
• Moder K G, Luthra H S, Kubo R, Griffiths M M, David C S. Prevention of collagen-induced arthritis in mice by treatment with an antibody directed against the T cell receptor αβ framework. Autoimmun 1992; 11: 219–224
   PubMed Web of Science ®Google Scholar
• Banerjee S, Haqqi T M, Luthra H S, Stuart J M, David C S. Possible role of Vβ T cell receptor genes in susceptibility to collagen-induced arthritis in mice. J Exp Med 1988; 167: 832–839
   PubMed Web of Science ®Google Scholar
• Haqqi T M, Banerjee S, Anderson G D, David C S. RIII S/J (H-2′): an inbred mouse strain with a massive deletion of T cell receptor Vβ genes. J Exp Med 1989; 169: 1903–1909
   PubMed Web of Science ®Google Scholar
• Haqqi T M, David C S. T cell receptor Vβ genes repertoire in mice. Possible role in resistance and susceptibility to type II collagen-induced arthritis. J Autoimmun 1990; 3: 113–121
   PubMed Web of Science ®Google Scholar
• Anderson G D, Banerjee S, David C S. MHC class II Aα, Ea molecules determine the clonal deletion of Vβ6+ T cells: studies with recombinant and transgenic mice. J Immunol 1989; 143: 3757–3761
   PubMedGoogle Scholar
• MacDonald H R, Schneider R, Lee R K, Howe R C, Acha-Orbea H, Festenstein H, Zinkernagel R M, Hengartner H. T-cell receptor Vβ use predicts reactivity and tolerance to Mls-la-encoded antigens. Nature 1988; 332: 40–45
   PubMed Web of Science ®Google Scholar
• Kappler J W, Staerz U, White J, Marrack P C. Self-tolerance eliminates T cells specific for Mls-modified products of the major histocompatibility complex. Nature 1988; 332: 35–40
   PubMed Web of Science ®Google Scholar
• Griffiths M M, Eichwald U, Martin J M, Smith C B, DeWitt C W. Immunogenetic control of experimental type II collagen induced arthritis. I. Susceptibility and resistance among inbred strains of rats. Arthritis Rheum 1981; 24: 871–879
   Google Scholar
• Cole B C, Washburn L R. Evaluation of arthritogenic properties of mycoplasmas for small laboratory animals. Methods in Mycoplasmology. Academic Press, New York and London, Vol 11: 305–310
   Google Scholar
• Griffiths M M, DeWitt C W. Immunogenetic control of experimental collagen induced arthritis in rats. II. ECIA susceptibility and immune response to type II collagen (calf) are linked to RTI. J Immunogenet 1981; 8: 463–470
   PubMedGoogle Scholar
• Goldschmidt T J, Holmdahl R. Anti-T cell receptor treatment of rats with established autologous collagen induced arthritis: suppression of arthritis without reduction of anti-type II collagen autoantibody levels. Eur J Immunol 1991; 21: 1327–1330
   PubMed Web of Science ®Google Scholar
• Yoshino S, Cleland L G, Mayrhofer G. Treatment of collagen induced arthritis in rats with a monoclonal antibody against the alpha beta T cell antigen receptor. Arthritis Rheum 1991; 34: 1039–1047
   PubMedGoogle Scholar
• Banerjee S, Anderson G D, Luthra H S, David C S. Influence of complement C5 and Vβ T cell receptor mutations on susceptibility to collagen-induced arthritis in mice. J Immunol 1989; 142: 2237–2243
   PubMedGoogle Scholar
• Spinella D G, Jeffers J R, Reife R A, Stuart J M. The role of C5 and T-cell receptor Vβ genes in susceptibility to collagen-induced arthritis. Immunogen 1991; 34: 23–27
   PubMedGoogle Scholar
• Chiocchia G, Boissier M-C, Fournier C. Therapy against murine collagen-induced arthritis with T cell receptor Vβ-specific antibodies. Eur J Immunol 1991; 21: 2899–2905
   PubMed Web of Science ®Google Scholar
• Mori L, Loetscher H, Kakimoto K, Bluethmann H, Steinmetz M. Expression of a transgenic T cell receptor β chain enhances collagen-induced arthritis. J Exp Med 1992; 176: 381–388
   PubMedGoogle Scholar
• Andersson M, Goldschmidt T J, Michaelsson E, Larsson A, Holmdahl R. T cell receptor V beta haplotype and complement component C5 play no significant role for the resistance to collagen induced arthritis in the SWR mouse. Immunol 1991; 73: 191–196
   PubMedGoogle Scholar
• Moder K G, Luthra H S, Griffith M M, David C S. Prevention of collagen-induced arthritis in mice by deletion of T cell receptor Vβ8 bearing T cells with monoclonal antibodies. British Journal of Rheumatology 1992, (In Press)
   Google Scholar
• Anderson G D, Banerjee S, Luthra H S, David C D. Role of mls-Ia locus and clonal deletion of T cells in susceptibility to collagen induced arthritis in mice. J Immunol 1991; 147: 1189–93
   PubMed Web of Science ®Google Scholar
• Haqqi Y M, Anderson G D, Banerjee S, David C S. Restricted heterogeneity in T cell receptor VP gene usage in the lymph nodes and arthritic joints of mice. Proc Narl Acad Sci USA 1992; 89: 1253–1255
   PubMed Web of Science ®Google Scholar
• Behlke M A, Chou H S, Huppi K, Loh D Y. Murine T cell receptor mutants with deletions of β chain variable region genes. Proc Natl Acad Sci USA 1986; 83: 761–771
   Google Scholar
• Terato K, Seyer J M, Makino H, Crerner M A, Hasty D, Stuart J M, Kang A H. Identification of epitopes within the CB-11 region of type II collagen important for collagen induced arthritis. Arthritis Rheum 1991; 34(Suppl)S66
   Google Scholar
• Wooley P H, Luthra H S, Griffiths M M, Stuart J M, Huse A, David C S. Type II collagen-induced arthritis in mice. IV. variations in immunogenetic regulation provide evidence for multiple arthritogenic epitopes on the collagen molecule. J Immunol 1985; 135: 2443–2451
   PubMed Web of Science ®Google Scholar
• Griffiths M M, Cremer M A, Harper D S, McCall S, Cannon G W. Immunogenetics of collagen induced arthritis in rats. Both MHC and non-MHC gene products determine the epitope specificity of immune responses to bovine and chick type II collagens. J Immunol 1992; 149: 309–316
   PubMed Web of Science ®Google Scholar
• Burkhwdt H, Holmdahl R, Deutzmann R, Wiedemann H, von der Mark H. Identification of a major antigenic epitope on CNBr-fragment 11 of type II collagen recognized by murine autoreactive B cells. Eur J Immunol 1991; 21: 49–54
   PubMedGoogle Scholar
• Watson W C, Brown P S, Pitcock J A, Townes A S. Passive transfer studies with type II collagen antibody in B10.D2/old and new line C57BL/6 normal and beige (Chediack-Higadi) strains: evidence of important roles of C5 and multiple inflammation cell types in the development of erosive arthritis. Arthritis Rheum 1987; 30: 460–470
   PubMed Web of Science ®Google Scholar
• Watson W C, Townes A S. Genetic susceptibility to murine collagen II autoimmune arthritis: proposed relationship to the IgG2 autoantibody subclass response, complement C5, major histocompatibility complex (MHC), and non-MHC loci. J Exp Med 1985; 162: 1878–1891
   PubMed Web of Science ®Google Scholar
• Holmdahl R, Jansson L, Andersson M. Female sex hormones suppress development of collagen-induced arthritis in mice. Arthritis Rheum 1986; 29: 1501–1509
   PubMed Web of Science ®Google Scholar
• Bossier M C, Feng X Z, Carlioz A, Roudier R, Fournier C. Experimental autoimmune arthritis in mice. I. Homologous type II collagen is responsible for self-perpctuating chronic arthritis. Ann Rheum Dis 1987; 46: 691–700
   PubMedGoogle Scholar
• Sternberg E M, Hill J M, Chrousos G P, Kamilaris T, Listwak S J, Gold P W, Wilder R L. Inflammatory mediator-induced hypo-thalamic-pituitary-adrenal axis activation is defective in strep-tococcal cell wall arthritis-susceptible Lewis rats. Proc Natl AcadSci USA 1989; 86: 2374–2378
   PubMed Web of Science ®Google Scholar
• Erickson R P, Tachibana D K, Herzenberg A, Rosenberg L T. A single gene controlling hemolytic complement and a serum antigen in the mouse. J Immunol 1963; 92: 611–622
   Google Scholar
• Cinader B, Dubiski S, Wardlaw A C. Distribution, inheritance, and properties of an antigen. MUBI, and its relation to hemolytic complement. J Exp Med 1964; 120: 897–905
   PubMedGoogle Scholar
• Pfeiffer C, Murray J, Madri J, Bottomly K. Selective activation of Th-l and Th2-like cells in vivo. Response to human collagen IV. Immunological Rev 1991; 123: 65–84
   PubMedGoogle Scholar
• Herman A, Kappler J W, Marrack P, Pullen A M. Superantigens: mechanisms of T-cell stimulation and role in immune responses. Ann Rev Immunol 1991; 9: 745–772
   PubMed Web of Science ®Google Scholar
• Friedman S M, Posnett D N, Tumang J R, Cole B C, Crow M K. A potential role for microbial superantigens in the pathogenesis of systemic autoimmune disease. Arthritis Rheum 1991; 34: 468–480
   PubMed Web of Science ®Google Scholar
• Paliard X, West S G, Lafferty J A, Clements J R, Kappler J W, Marrack P, Kotzin B L. Evidence for the effects of a super-antigen in rheumatoid arthritis. Science 1991; 253: 325–329
   PubMed Web of Science ®Google Scholar
• Frankel W N, Rudy C, Coffin J M, Huber B. Linkage of Mls genes to endogenous mammary tumor viruses of inbred mice. Nature 1991; 349: 526–528
   PubMed Web of Science ®Google Scholar
• Wooley P H, Whalen J D, Karvonen R L, David C S. Mls pheno-type influences susceptibility to proteoglycan-induced arthritis in mice. Arthritis Rheum 1991; 34(Suppl)S67
   Google Scholar
• Wooley P H, Whalen J D, David C S. The Mls gene locus regulates susceptibility to pristane-induced arthritis in mice. Arthritis Rheum 1991; 34(Suppl)S66
   Google Scholar
• Woodland D L, Happ M P, Gollob K J, Palmer E. An endogenous retrovirus mediating deletion of aβ T cells. Nature 1991; 349: 529–530
   PubMed Web of Science ®Google Scholar
• Cole B C, Atkin C L. The Mycoplosma arthritidis T cell mitogen, MAM: A model superantigen. Immunol Today 1991; 12: 271–276
   PubMedGoogle Scholar
• Cole B C. The immunobiology of Mycoplasma arthritidis and its superantigen MAM. Current contents in Microbiology and Immunology 1992; 164: 107–119
   Google Scholar
• Cole B C, Griffiths M M, Sullivan G J, Ward J T. Role of non-RT1 genes in the response of rat lymphocytes to Mycoplosmo arthritidis T cell mitogen, concanavalin A, and phytohemag-glutinin. J Immunol 1986; 136: 2364–2369
   PubMedGoogle Scholar
• Baccala L, Smith L R, Vestberg M, Peterson P A, Cole B C, Theofilopoulos A N. Mycoplasma arthritidis mitogen: Vβ engaged in mice, rats and humans, and requirement for HLA-DRa for presentation. Arthritis Rheum 1992; 35: 434–442
   PubMedGoogle Scholar
• Howell M D, Diveley J P, Lundeen K A, Esty A, Winters S T, Carlo D J, Brostoff S M. Limited T cell receptor B-chain heterogeneity among IL-2R synovial T cells suggests a role for superantigen in rheumatoid arthritis. PNAS 1991; 88: 10921–10925
   PubMed Web of Science ®Google Scholar