Bystander CD8 T Cell-Mediated Demyelination After Viral Infection of the Central Nervous System
Author(s) -
Jodie S. Haring,
Lecia L. Pewe,
Stanley Perlman
Publication year - 2002
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.169.3.1550
Subject(s) - multiple sclerosis , bystander effect , immune system , immunology , cd8 , inflammation , biology , mouse hepatitis virus , t cell , virus , central nervous system , genetically modified mouse , cytotoxic t cell , virology , disease , medicine , transgene , gene , pathology , neuroscience , infectious disease (medical specialty) , genetics , covid-19 , in vitro
Multiple sclerosis, a chronic inflammatory disease of the CNS, is characterized by immune-mediated demyelination. Many patients have a remitting-relapsing course of disease with exacerbations often following unrelated microbial illnesses. The relationship between the two events remains obscure. One possibility is that T cells specific for the inciting microbial pathogen are able to effect demyelination at a site of ongoing inflammation within the CNS. This possibility was examined in mice infected with mouse hepatitis virus, a well-described model of virus-induced demyelination. Using transgenic TCR/recombination activation gene 2(-/-) mice with only non-mouse hepatitis virus-specific T cells, we show that CD8 T cells are able to cause demyelination in the absence of cognate Ag in the CNS, but only if specifically activated. These findings demonstrate a novel mechanism for immune-mediated neuropathology and show that activated CD8 T cells may serve as important mediators of bystander demyelination during times of infection, including in patients with multiple sclerosis.
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