Viruses and Autoimmunity
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Tài liệu tham khảo
Antigenic variation in infectious diseases, T H Birkbeck, C W Penn. IRL Press, OxfordUK 1986
Virus Persistence, B WJ Mahy, A C Minson, G K Darby. Cambridge Univ Press, CambridgeUK 1983, SGM symposium 33
Izui S, Hari I, Le Ming Hang, Elder J H, McConahey P J, Doxon R J. Association of elevated serum glycoprotein gp70 with increased gp70 immune complex formation and accelerated lupus nephritis in autoimmune male BXSB mice. Clin Exp Immunol 1984; 56: 272–280
Rhodes G D, Carson D A, Valbracht H, Houghton R, Vaughan J H. Human immune responses to synthetic peptides from the Epstein Barr nuclear antigen. J Immunol 1985; 134: 211–216
Depper J M, Blustein H G, Zvaifler N J. Impaired regulation of Epstein Barr virus-induced lymphocyte proliferation in rheumatoid arthritis is due to a T cell defect. J Immunol 1987; 127: 1899–1902
Fox R I, Chilton T, Rhodes G, Vaughan J H. Lack of reactivity of rheumatoid arthritis synovial membrane DNA with cloned Epstein Barr virus DNA probes. J Immunol 1986; 137: 498–501
Hamerman D, Gresser I, Smith C. Isolation of cytomegalovirus from synovial cells of a patient with rheumatoid arthritis. J Rheumatol 1982; 95: 658–663
Johannson P JH, Schroder A K, Nardella F A, Mannik M, Christensen P. Interaction between Herpes simplex type I and induced Fc receptor and rabbit immunoglobulin G (IgG) domain. Immunology 1986; 58: 251–255
Moore K W, Jardieu P, Mietz J A, Tounstine M L, Kuff E L, Ishizaka K, Martens C L. Rodent IgE-binding factor genes are members of an endogenous retrovirus-like gene family. J Immunol 1986; 136: 4283–4289
Mathews M B, Bernstein R M. Myositis autoantibody inhibits histidyl-tRNA synthetase: a model for autoimmunity. J Exp Med 1986; 163: 1281–1291
Woodruff J F. Viral myocarditis. A review. Amer J Pathol 1980; 101: 427–479
Rose N R, Biesel K W, Herskowitz A, Neu N, Wolfgram L J, Alvarez F L, Traystman M D, Craig S W. Cardiac myosin and autoimmune myocarditis. Autoimmunity and Autoimmune Disease. John Wiley and Sons, Chichester 1987; 3–24, (Ciba Foundation Symposium 129)
Lodge P A, Herzum M, Olszewiski J, Huber S A. Coxsackievirus B-3 myocarditis. Acute and chronic forms of the disease caused by different immunopathogenic mechanisms. Amer J Pathol 1987; 128: 455–463
Huber S A, Heintz N, Tracy R, Coxsackie B. Induced myocarditis: virus and actinomycin D treatment of myocytes induces novel antigens recognized by cytolytic T lymphocytes. J Immunol 1988; 141: 3214–3219
Maisch B, Trostel-Soeder R, Stechemesser E, Berg P A, Kochsiek K. Diagnostic relevance of humoral and cell-mediated immune reactions in patients with acute viral myocarditis. Clin Exp Immunol 1982; 48: 533–545
Neu N, Craig S W, Rose N R, Alvarez F, Beisel K W. Coxsackievirus induced myocarditis in mice: cardiac myosin autoantibodies do not cross-react with the virus. Clin Exp Immunol 1987; 69: 566–574
Craighead J E, Steinke J. Diabetes mellitus-like syndrome in mice infected with encephalomycarditis virus. Amer J Pathol 1971; 63: 119–134
Lipton H, Miller S, Melveld R, Fujinami R S. Theiler's murine encephalomyelitis virus (TMEV) infection in mice as a model for multiple sclerosis. Concepts in Viral Pathogenesis II, A L Notkins, M BA Oldstone. Springer-Verlag, New York 1986; 248–254
Miller S D, Clatch R J, Pevear D C, Trotter J L, Lipton H L. Class II-restricted T cell responses in Theiler's murine encephalomylitis virus (TMEV)-induced demyelinating disease. I. Cross-specifity among TMEV substrains and related picronaviruses but not myelin proteins. J Immunol 1987; 138: 3776–3184
Rodriguez M, Pierce M L, Howie E A. Immune response gene products (la antigens) on glial and endothelial cells in virus-induced demyelination. J Immunol 1987; 138: 3438–3442
Johnson R T, Griffin D E. Virus induced autoimmune demyelinating disease of the central nervous system. Concepts in Viral Pathogenesis II, A L Notkins, M BA Oldstone. Springer Verlag, New York 1986; 203–209
Mokhtarian F, Swoveland P. Predisposition to EAE induction in resistant mice by prior infection with Semliki forest virus. J Immunol 1987; 138: 3264–3268
Nathanson N, Panitch H, Palsson P A, Petursson G, Georgsson G. Pathogenesis of Visna. II Effect of immunosuppression upon early central nervous system lesions. Lab Invest 1976; 35: 444–451
Panitch H, Petursson G, Georgsson G, Palsson P A, Nathanson N. Pathogenesis of Visna. III Immune responses to central nervous system antigens in experimental alergic encephalomyelitis and Visna. Lab Invest 1976; 35: 452–460
Yoon J W, Rodrigues M M, Curries C, Notkins A L. Long-term complications of virus-induced diabetes in mice. Narure 1982; 296: 566–569
Leiter E H, Kuff E L. Intracisternal type A particles in murine pancreatic B cells. Immunocytochemi-cal demonstration of increased antigen (p73) in genetically diabetic mice. Amer J Path 1984; 114: 46–55
Debray-Sachs M, Sai P, Botard C, Assan R, Hamburger J. Anti-pancreatic immunity in genetically deficient diabetic mice. Clin Exp Immunol 1983; 51: 1–7
Leiter E H. Type C retrovirus production by pancreatic beta cells. Association with accelerated pathogenesis in C3H-db/db (“diabetes”) mice. Amer J Pathol 1985; 119: 22–32
Yale J-F, Marliss E B. Review. Altered immunity and diabetes in the BB rat. Clin Exp Immunol 1984; 57: 1–11
Weetman A P, Smallridge R C, Nutman T B, Burman K D. Persistent thyroid autoimmunity after subacute thyroiditis. J Clin Lab Immunol 1987; 23: 1–6
Pflatz M, Hedinger C E. Abnormal basement membrane structures in autoimmune thyroid disease. Lab Invest 1986; 55: 531–539
Robertson D AF, Guy E C, Zhang S L, Wright R. Persistent measles virus genome in autoimmune chronic active hepatitis. Lancet, ii: 9–11