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. 2002 Dec 9;140(2):196–201. doi: 10.1016/0923-2494(89)90086-2

Sites of antigen presentation in T-cell mediated demyelinating diseases

PT Massa 1
PMCID: PMC7135488  PMID: 2662284

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References

  1. Clatch R.J., Melvold R.W., Dal Canto M.C., Miller S.D., Lipton H.L. The Theiler's murine encephalomyelitis virus (TMEV) model for multiple sclerosis shows a strong influence of the murine equivalents of HLA-A, B, and C. J. Neuroimmunol. 1987;15:121–135. doi: 10.1016/0165-5728(87)90087-7. [DOI] [PubMed] [Google Scholar]
  2. Crawford R.M., Finbloom D.S., O'Hara J., Paul W.E., Meltzer M.S. B-cell stimulatory factor-1 (interleukin 4) activates macrophages for increased tumoricidal activity and expression of Ia antigens. J. Immunol. 1987;139:135–141. [PubMed] [Google Scholar]
  3. Fontana A., Erb P., Pircher H., Zinkernagel R., Weber E., Fierz W. Astrocytes as antigen-presenting cells. Part II: unlike H-2K-dependent cytotoxic T cells, H-2 Ia-restricted T cells are only stimulated in the presence of interferon-gamma. J. Neuroimmunol. 1986;12:15–28. doi: 10.1016/0165-5728(86)90093-7. [DOI] [PubMed] [Google Scholar]
  4. Fontana A., Fierz W., Wekerle H. Astrocytes present myelin basic protein to encephalitogenic T-cell lines. Nature (Lond.) 1984;307:273–276. doi: 10.1038/307273a0. [DOI] [PubMed] [Google Scholar]
  5. Haase A.T. Pathogenesis of lentivirus infections. Nature (Lond.) 1986;322:130–136. doi: 10.1038/322130a0. [DOI] [PubMed] [Google Scholar]
  6. Johnson R.T., Griffin D.E., Hirsch R.L., Wolinsky J.S., Roedenbeck S., Lindo de Soriano I., Vaisberg A. Measles encephalomyelitis: clinical and immunological studies. New Engl. J. Med. 1984;310:137–141. doi: 10.1056/NEJM198401193100301. [DOI] [PubMed] [Google Scholar]
  7. Kim S.U., Moretto G., Shin D.H. Expression of Ia antigens on the surface of human oligodendrocytes and astrocytes in culture. J. Neuroimmunol. 1985;10:141–149. doi: 10.1016/0165-5728(85)90004-9. [DOI] [PubMed] [Google Scholar]
  8. Liebert U.G., 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. doi: 10.1016/0165-5728(88)90018-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lisak R., Hirayama M., Kuchmy D., Rosenzeig A., Kim S.U., Pleasure D., Silberberg D. Cultured human and rat oligodendrocytes and rat Schwann cells do not have immune response gene-associated antigen (Ia) on their surface. Brain Res. 1983;289:285–292. doi: 10.1016/0006-8993(83)90029-x. [DOI] [PubMed] [Google Scholar]
  10. Liu Y., King N., Kesson A., Blanden R.V., Mullbacher A. Flavivirus infection modulates cell surface MHC antigen expression on astrocytes. J. Neuroimmunol. 1987;16:109a. doi: 10.1016/0165-5728(89)90171-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Male D., Pryce G. Induction of Ia molecules on brain endothelium is related to susceptibility to experimental allergic encephalomyelitis. J. Neuroimmunol. 1989;21:87–90. doi: 10.1016/0165-5728(89)90163-x. [DOI] [PubMed] [Google Scholar]
  12. Massa P.T., Brinkmann R., ter Meulen V. Inducibility of Ia antigen on astrocytes by murine coronavirus JHM is rat-strain dependent. J. exp. Med. 1987;166:259–264. doi: 10.1084/jem.166.1.259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Massa P.T., Dorries R., ter Meulen V. Viral particles induce Ia antigen expression on astrocytes. Nature (Lond.) 1986;320:543–546. doi: 10.1038/320543a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Massa P.T., Schimpl A., Wecker E., ter Meulen V. Vol. 84. 1987. Tumor necrosis factor amplified measles-virus-mediated Ia induction on astrocytes; pp. 7242–7245. (Proc. nat. Acad. Sci. (Wash.)). [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Massa P.T., ter Meulen V., Fontana A. Vol. 84. 1987. Hyperinducibility of Ia antigen on astrocytes correlates with strain-specific susceptibility to experimental autoimmune encephalomyelitis; pp. 4219–4223. (Proc. nat. Acad. Sci. (Wash.)). [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Massa P.T., Wege H., ter Meulen V. Analysis of murine hepatitis virus (JHM strain) tropism toward Lewis rat glial cells in vitro: type I astrocytes and brain macrophages (microglia) as primary glial cell targets. Lab. Invest. 1986;55:318–327. [PubMed] [Google Scholar]
  17. McCarron R.M., Spatz M., Kempski O., Hogan R.N., Meuhl L., McFarlin D.E. Interaction between myelin-basic-protein-sensitized T lymphocytes and murine cerebral vascular endothelial cells. J. Immunol. 1986;137:3428–3435. [PubMed] [Google Scholar]
  18. McFarlin D.E., McFarland H.F. Multiple sclerosis. New Engl. J. Med. 1982;307:1183–1188. doi: 10.1056/NEJM198211043071905. [DOI] [PubMed] [Google Scholar]; McFarlin D.E., McFarland H.F. Multiple sclerosis. New Engl. J. Med. 1982;307:1246–1251. doi: 10.1056/NEJM198211113072005. [DOI] [PubMed] [Google Scholar]
  19. Narayan O., Wolinski J.S., Clements J.E., Strandberg J.D., Griffin D.E., Cork L.C. Slow virus replication: the role of macrophages in the persistence and expression of visna virus of sheep and goats. J. gen. Virol. 1982;59:345–356. doi: 10.1099/0022-1317-59-2-345. [DOI] [PubMed] [Google Scholar]
  20. Oldstone M.B.A., Blount P., Southern P.J., Lampert P.W. Cytoimmunotherapy for persistent virus infection reveals a unique clearance pattern from the central nervous system. Nature (Lond.) 1986;321:239–243. doi: 10.1038/321239a0. [DOI] [PubMed] [Google Scholar]
  21. Paterson P.Y. Experimental autoimmune (allergic) encephalomyelitis. In: Miescher P.A., Mueller-Eberhard H.J., editors. Textbook of Immunopathology. Grune and Stratton; New York: 1976. pp. 179–213. [Google Scholar]
  22. Prineas J.W., Kwon E.E., Cho E.-S., Sharer L.R. In: Multiple Sclerosis: experimental and clinical aspects. Scheinberg L.C., Raine C.S., editors. Annals of the New York Academy of Sciences; New York: 1984. pp. 11–33. [Google Scholar]
  23. Rammohan K.W., McFarlin D.E., McFarland H.F. Chronic measles encephalitis in mice. J. infect. Dis. 1980;142:608–613. doi: 10.1093/infdis/142.4.608. [DOI] [PubMed] [Google Scholar]
  24. Rodriguez M., Leibowitz J., David C.S. Susceptibility to Theiler's-virus-induced demyelination. Mapping of the gene within the H-2D region. J. exp. Med. 1986;163:620–631. doi: 10.1084/jem.163.3.620. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Schnitzer J., Schachner M. Expression of Thy-1, H-2 and NS-4 cell surface antigens and tetanus toxin receptors in early postnatal and adult mouse cerebellum. J. Neuroimmunol. 1981;1:429–456. doi: 10.1016/0165-5728(81)90022-9. [DOI] [PubMed] [Google Scholar]
  26. Springer T.A., Dustin M.L., Kishimoto T.K., Marlin S.D. The lymphocyte function-associated LFA-1, CD-2, and LFA-3 molecules: cell adhesion receptors of the immune system. Ann. Rev. Immunol. 1987;5:223–252. doi: 10.1146/annurev.iy.05.040187.001255. [DOI] [PubMed] [Google Scholar]
  27. Sun D., Wekerle H. Ia-restricted encephalitogenic T lymphocytes mediating EAE lyse autoantigen-presenting astrocytes. Nature (Lond.) 1986;320:70–72. doi: 10.1038/320070a0. [DOI] [PubMed] [Google Scholar]
  28. Suzumura A., Lavi E., Weiss S.R., Silberberg D.H. Coronavirus infection induces H-2 antigen expression on oligodendrocytes and astrocytes. Science. 1986;232:991–993. doi: 10.1126/science.3010460. [DOI] [PubMed] [Google Scholar]
  29. Traugott U., Reinherz E.L., Raine C.S. Multiple sclerosis: distribution of T cells, T-cell subsets and Ia-positive macrophages in lesions of different ages. J. Neuroimmunol. 1983;4:201–221. doi: 10.1016/0165-5728(83)90036-x. [DOI] [PubMed] [Google Scholar]
  30. Traugott U. Multiple sclerosis: relevance of class I and class II MHC-expressing cells to lesion development. J. Neuroimmunol. 1987;16:283–302. doi: 10.1016/0165-5728(87)90082-8. [DOI] [PubMed] [Google Scholar]
  31. Watanabe R., Wege H., ter Meulen V. Adoptive transfer of EAE-like lesions from rats with coronavirus-induced demyelinating encephalomyelitis. Nature (Lond.) 1983;305:150–153. doi: 10.1038/305150a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Wege H., Watanabe R., ter Meulen V. Relapsing subacute demyelinating encephalomyelitis in rats during the course of coronavirus JHM infection. J. Neuroimmunol. 1984;6:325–336. doi: 10.1016/0165-5728(84)90022-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Williams K.A., Hart D.N.J., Fabre J.W., Morris P.J. Distribution and quantitation of HLA-ABC and DR (Ia) antigens on human kidney and other tissues. Transplantation. 1980;29:274–279. doi: 10.1097/00007890-198004000-00002. [DOI] [PubMed] [Google Scholar]
  34. Williams R.M., Lees M.B., Cambi F., Macklin W.B. Chronic experimental allergic encephalomyelitis induced in rabbits with bovine white matter proteolipid apoprotein. J. Neuropath. Exp. Neurol. 1982;41:508–521. doi: 10.1097/00005072-198209000-00004. [DOI] [PubMed] [Google Scholar]
  35. Wong G.H.W., Bartlett P.F., Clark-Lewis I., McKimm-Breshkin J.L., Schrader J.W. Interferon-gamma induces the expression of H-2 and Ia antigens on brain cells. J. Neuroimmunol. 1985;7:255–278. doi: 10.1016/s0165-5728(84)80026-0. [DOI] [PubMed] [Google Scholar]
  36. Yoshimura T., Kunishiha T., Sakai K., Endoh M., Namikowa T., Tabira T. Chronic experimental allergic encephalomyelitis in guinea pigs induced by proteolipid protein. J. Neurol. Sci. 1985;69:47–58. doi: 10.1016/0022-510x(85)90006-1. [DOI] [PubMed] [Google Scholar]

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