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10.1099/0022-1317-71-11-2565

http://scihub22266oqcxt.onion/10.1099/0022-1317-71-11-2565
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1979346!ä!1979346

suck abstract from ncbi


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pmid1979346      J+Gen+Virol 1990 ; 71 ( Pt 11) (ä): 2565-73
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  • Borna disease virus-induced meningoencephalomyelitis caused by a virus-specific CD4+ T cell-mediated immune reaction #MMPMID1979346
  • Richt J; Stitz L; Deschl U; Frese K; Rott R
  • J Gen Virol 1990[Nov]; 71 ( Pt 11) (ä): 2565-73 PMID1979346show ga
  • After intracerebral inoculation of Borna disease virus (BDV). Lewis rats develop a persistent infection of the central nervous system which is pathohistologically represented by perivascular encephalitic lesions predominantly in the grey matter. In previous studies it has been shown that a cell-mediated immune response causes Borna disease (BD). In order to define further the immune cell responsible for this immunopathological disease, a BDV-specific T cell line, NM1, was established and cultured in vitro. Phenotypically this T cell line was characterized by cytofluorometry as CD4-positive (CD4+). Proliferation assays with syngeneic and allogeneic antigen-presenting cells, and blocking experiments with monoclonal antibodies, revealed major histocompatibility complex class II antigens to be restriction elements. After passive transfer of this virus-specific CD4+ T cell into immunosuppressed BDV-infected recipients, full-blown disease could be induced. Immunohistological examination of the cells involved in perivascular inflammatory infiltrates in BDV-infected rats and in recipients of the NM1 T cell line revealed a dominance of macrophages and CD4+ T cells. The presence of these cells in encephalitic lesions strongly suggests a delayed type of hypersensitivity reaction as the pathogenetic mechanism of BD.
  • |Animals[MESH]
  • |Antibodies, Monoclonal/immunology[MESH]
  • |Antigen-Presenting Cells/immunology/microbiology[MESH]
  • |Antigens, Viral/*analysis[MESH]
  • |Astrocytes/immunology/microbiology[MESH]
  • |Binding, Competitive[MESH]
  • |Borna disease virus/*immunology[MESH]
  • |CD4-Positive T-Lymphocytes/*immunology/microbiology[MESH]
  • |Cell Line[MESH]
  • |Histocompatibility Antigens Class II/analysis[MESH]
  • |Hypersensitivity, Delayed/immunology[MESH]
  • |Lymphocyte Activation[MESH]
  • |Meningoencephalitis/etiology/*immunology/microbiology[MESH]
  • |Rats[MESH]


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