Summary
The recovery from viral infections is a result of complex interactions between specific and nonspecific host immunoreactions and the infectious agent. A variety of immune mechanisms are important factors in this event and operate together in overcoming the infectious process. Although much is known about viral defense mechanisms, it has proved remarkably difficult to assign a determinative role in vivo to any single immunological antiviral mechanism in recovery from a viral disease. Furthermore, the immune response to the virus itself may contribute to disease pathology. If vims induced immune responses are also directed against normal host components, autoimmune disease may develop. In this context measles virus (MV), which still causes significant morbidity and mortality despite the availablility of a live vaccine, is of interest because a well known complication of many cases of acute measles is postinfectious encephalomyelitis (acute measles encephalomyelitis). A cell-mediated immune response against myelin basic protein (MBP) has been detected in this disease and such an autoimmune response can lead to allergic encephalitis (EAE) as was shown in our animal model of MV-induced encephalitis. Further evidence for its pathogenetic role is provided by observations that (1) MV can substitute for sequences from the encephalitogenic region of MBP in the induction of EAE, and (2) some animals enter a refractory state for EAE following infection with recombinant MV nucleocapsid protein. In the following pages virological and immunological findings of MV infections in a rat model in relation to autoimmune reactions will be presented and the mechanisms by which measles virus may alter host reactivity against self-antigens discussed.
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References
Mitchell CD, Balfour HH: Measles control: so near and yet so far. Progr Med Virol 1985: 31: 1–42.
Schneider-Schaulies S, ter Meulen V: Molecular aspects of measles virus-induced central nervous system diseases. in: Roos RP (ed): Molecular Neurovirology, Humana Press, Totowa, New Jersey, USA, 1992, 419–448.
ter Meulen V, Stephenson JR: The possible role of viral infections in MS and other related demyelinating diseases. in Hallpike JF, Adams CWM, Tourtellotte WW (eds): Multiple Sclerosis, Chapman and Hall, London, 1983, pp. 241–274.
Cosby SL, McQuaid S, Taylor MJ, Bailey M, Rima BK, Martin SJ, and Allen IV: Examination of eight cases of multiple sclerosis and 56 neurological and non-neurological controls for genomic sequences of measles virus. J Gen Virol 1989: 70: 2027–2036.
Haase AT, Ventura P, Gibbs CJ Jr, Tourtellotte WW: Measles virus nucleotide sequences: detection by hybridization in situ. Science 1981: 212: 672–675.
Basle MF, Fournier JG, Rozenblatt S, Rebel A, Bouteille M: Measles virus RNA detected in Paget’s disease bone tissue by in situ hybridization. J Gen Virol 1986: 67: 907–913.
McKenna MJ, Mills BG: Immunohistochemical evidence of measles virus antigens in active otosclerosis. Otolaryngol. Head Neck Surg 1989: 101: 415–421.
Andjaparidze OG, Chaplygina NM, Bogomolova NN, Koptyaeva IB, Nevryaeva EG, Filimova RG, Tareeva IE: Detection of measles virus genome in blood leucocytes of patients with certain autoimmune diseases. Arch Virol 1989: 105: 287–291.
Robertson DAF, Guy EC, Zhang SL, Wright R: Persistent measles virus genome in autoimmune chronic active hepatitis. Lancet 1987: ii: 9–11.
Black FL, Persistent measles virus genome in autoimmune chronic active hepatitis: cause or coincidence? Hepatology 1988: 8: 186–187.
Johnson RT, Griffin DE, Hirsch RL, Wolinsky JS, Roedenbeck S, de Soriano IL, Vaisberg A: Measles Encephalomyelitis-clinical and immunologic studies. N Engl J Med 1984: 310: 137–141.
Gendelman H, Wolinsky JS, Johnson RT, Pressman NJ, Pezeshkpour GH, Boisset GF: Measles encephalitis: Lack of evidence of viral invasion of the central nervous system and quantitative study of the nature of demyelination. Ann Neurol 1984: 15: 353–360.
Griffin DE, Ward BJ, Jauregui E, Johnson RT, Vaisberg A: Immune activation during measles. N Engl J Med 1989: 320: 1667–1672.
Griffin DE, Cooper SJ, Hirsch RL, Johnson RT, de Soriano IL, Roedenbeck S, Vaisberg A: Changes in plasma IgE levels during complicated and uncomplicated measles virus infections. J Allergy Clin Immunol 1985: 76: 206–213.
Johnson RT, Griffin D: Virus-induced autoimmune demyelinating disease of the CNS. in Notkins AL, Oldstone MBA (eds): Concepts in Viral Pathogenesis II, Springer Verlag, New York, 1986 pp. 203–209.
Liebert UG, Meulen ter V: Virological aspects of measles virus induced encephalomyelitis in Lewis and BN rats. J gen Virol 1987: 68: 1715–1722.
Schneider-Schaulies S, Liebert UG, Baczko K, Cattaneo R, Billeter M, Meulen ter V: Restriction of measles virus gene expression in acute and subacute encephalitis of Lewis rats. Virol 1989: 171: 525–534.
Raine CS: Biology of disease. Analysis of autoimmune demyelination: its impact upon Multiple Sclerosis. Lab Invest 1984: 50: 608–635.
Yamamura T, Namikawa T, Endoh M, Kunishita T, Tabira T: Experimental allergic encephalomyelitis induced by proteolipid apoprotein in Lewis rats. J Neuroimmunol 1986: 12: 143–153.
Itoyama Y, Webster H de F.: Immunocytochemical study of myelin-associated glycoprotein (MAG) and basic protein (BP) in acute experimental allergic encephalomyelitis (EAE). J Neuroimmunol 1982: 3: 351–364.
Vandenbark AA, Gill T, Offner H: A myelin basic protein-specific T cell line that mediates experimental allergic autoimmune encephalomyelitis. J Immunol 1985: 135: 223–228.
Liebert UG, Linington C, ter Meulen V: Induction of autoimmune reactions to myelin basic protein in measles virus encephalitis in Lewis rats. J Neuroimmunol 1988: 17: 103–118.
Massanari RM, Paterson PY, Lipton HL: Potentiation of experimental allergic encephalomyelitis in hamsters with persistent encephalitis due to measles virus. J Infect Dis 1978: 139: 297–303.
Liebert UG, Hashim GA, Meulen ter V: Characterization of measles virus-induced cellular autoimmune reactions against myelin basic protein in Lewis rats. J Neuroimmunol 1990: 29: 139–147.
Offner H, Hashim G, Vandenbark AA: Response of rat encephalitogenic T lymphocyte lines to synthetic peptides of myelin basic protein. J Neurosci Res 1987: 17: 344–348.
Hashim GA, Day ED: Role of antibodies in T cell-mediated experimental allergic encephalomyelitis. J Neurosci Res 1988: 21: 1–5.
Liebert UG, ter Meulcn V: Synergistic interaction between measles virus infection and MBP peptide-specific T cells in the induction of EAE in Lewis rats. J. Neuroimmunol. 1993: 46, 217–224.
Brinckmann UG, Bankamp B, Reich A, ter Meulen V, Liebert UG: Efficacy of single measles virus structural proteins in the protection of rats from measles encephalitis. J. gen. Virol. 1991: 72, 2491–2500.
Levine S, Sowinski R: Experimental allergic encephalomyelitis in inbred and outbred mice. J Immunol 1973: 110: 139–143.
Levine S, Sowinski R: Allergic encephalomyelitis in the reputedly resistant Brown Norway strain of rats. J Immunol 1975: 114: 597–601.
Hirsch MS, Proffitt MR: Autoimmunity in viral infection; in Notkins AL (ed): Viral Immunology and Immunopathology, Academic Press, New York, 1975, pp.419–434.
Notkins AL, Onodcra T, Prabhaker BS: Virus-induced autoimmunity; in Notkins AL, Oldstone MBA (eds): Concepts in Viral Pathogenesis, Springer Verlag, New York, 1984, pp. 210–215.
Schattner A, Rager-Zisman B: Virus-induced autoimmunity. Rev Infect Dis 1990: 12: No. 2, 204–222.
Rosen A, Gergely P, Jondal M, Klein G, Britton S: Polyclonal Ig production after Epstein-Barr virus infection of human lymphocytes in vitro. Nature 1977: 267: 52–54.
Cherry JD: Viral infections: measles; in Feigin RD, Cherry JD (eds): Textbook of Pediatrie Infectious Diseases, Vol. 2, Saunders, Philadelphia, London, Toronto, Mexico City, Rio de Janeiro, Sydney, Tokyo, 1987, pp. 1607–1635.
Oldstone MBA, Notkins AL: Molecular mimicry; in Notkins AL, Oldstone MBA (eds): Concepts in Viral Pathogenesis, Springer Verlag, New York, 1986, pp. 195–202.
Jahnke U, Fischer EH, Alvord EC: Sequence homology between certain viral proteins and proteins related to encephalomyclilis and neuritis. Science 1985: 229: 282–284.
Weise MJ, Carnegie PR: An approach to searching protein sequences for superfamiliy relationships or chance similarities relevant to the molecular mimicry hypothesis: application to the basis proteins of myelin. J Neurochcm 1988: 51: 1267–1273.
Fujinami RS, Oldstone MBA: Amino acid homology and immune responses between the encephalitogenic site of myelin basic protein and virus: A mechanism for autoimmunity. Science 1985: 230: 1043–1045.
Wekerle H, Linington C, Lassmann H, Meyermann R: Cellular immune reactivity within the CNS. Trends Neurosci 1986: 9: 271–275.
Sedgwick JD, Dörrics R: The immune system response to viral infection of the CNS. Sem Neurosci 1991: 3: 93–100.
Wong GHW, Bartlett PF, Clark-Lewis I, McKimm-Breschkin JL, Schrader JW: Interferon-g induces the expression of H-2 and Ia antigens on brain cells. J Neuroimmunol 1985: 7: 255–278.
Hickey WF, Kimura H: Pcrivascular microglial cells of the CNS are bone marrow-derived and present antigen in vivo. Science 1988: 239: 290–292.
Hickey WF, Hsu BL, Kimura H: T-lymphocyte entry into the central nervous system. J Neurosci Res 1991: 28: 254–260.
Hart DNJ, Fahre JW: Demonstration and characterization of Ia-positive dendritic cells in the institial tissues of rat heart and oilier tissues, but not brain. J Exp Med 1981: 154: 347–361.
Traugott U, Scheinberg LC, Raine CS: On the presence of Ia-positive endothelial cells and astrocytes in multiple sclerosis lesions and its relevance to antigen presentation. J Neuroimmunol 1985: 8: 1–14.
Massa PT, Dörrics R, ter Mculcn V: Viral particles induce Ia antigen expression on astrocytes. Nature 1986: 320: 543–546.
Massa PT, Schimpl A, Wecker E, ter Meulen V: Tumor necrosis factor amplifies measles virus-mediated Ia induction on astrocytes. Proc Natl Acad Sci USA, 1987: 84: 7242–7245.
Fontana A, Fierz W, Wekerle H: Astrocytes present myelin basic protein to encephalitogenic T cell lines. Nature 1984: 307: 273–276.
Sedgwick JD, Mößner R, Schwender S, ter Meulen V: MHC-expressing non-hematopoietic astroglial cells prime only CD8+ T lymphocytes: Astroglial cells as perpetuators but not initiators of CD4+ T cell responses in the central nervous system. J Exp Med 1991: 173: 1235–1246.
Matsumoto Y, Ilara N, Tanaka R, Fujiwara M: Immunohistochemical analysis of the rat central nervous system during experimental allergic encephalomyelitis, with special reference to Ia-positive cells with dendritic morphology. J Immunol 1986: 136: 3668–3676.
Hayes GM, Woodroofe MN, Cuzner ML, Microglia are the major cell type expressing MHC class II in human white matter. J Neurol Sci 1987: 80: 25–37.
Sedgwick JD, Schwender S, Gregersen R, ter Meulen V: Constitutive MHC class II expression on ramified microglia from BN strain rats resistant to experimental autoimmune encephalomyelitis. J Exp Med 1993: in press.
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Liebert, U.G., ter Meulen, V. (1994). Measles Virus Induced Autoimmune Reactions against Brain Antigen. In: Salvati, S. (eds) A Multidisciplinary Approach to Myelin Diseases II. NATO ASI Series, vol 258. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-2435-9_13
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DOI: https://doi.org/10.1007/978-1-4615-2435-9_13
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