Medical College of Wisconsin
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CNS cell populations are protected from virus-induced pathology by distinct arms of the immune system. Brain Pathol 1999 Jan;9(1):21-31

Date

02/16/1999

Pubmed ID

9989447

Pubmed Central ID

PMC8098348

DOI

10.1111/j.1750-3639.1999.tb00206.x

Scopus ID

2-s2.0-0032958517 (requires institutional sign-in at Scopus site)   23 Citations

Abstract

The basis for the distinct patterns of brain pathology in individuals experiencing virus-induced encephalitis may be related to either the tropism of the virus or the host's response to virus infection of the central nervous system (CNS). In these studies we used Theiler's murine encephalomyelitis virus (TMEV) and a series of mice deficient in various immune system components (alpha/beta T cells, antibody, Class I MHC, and Class II MHC) to examine the hypothesis that discrete populations of CNS cells are protected differentially from virus infection by distinct arms of the immune response. Here we demonstrate that the Class I-mediated immune response provided more protection from areas of the brain (brainstem, corpus callosum and cerebellum) with abundant white matter as there was significantly more disease in these areas in beta2m -/- (Class I-deficient) mice as compared to A beta(0) (Class II-deficient) mice. In contrast, the striatum, with an abundance of neurons, was protected from virus-induced pathology primarily by antibody. In addition, we determined that antibody and alpha/beta T cells provided protection from severe deficits and death during the acute phase of the disease. The data presented here support the hypothesis that distinct immune system components function to protect discrete areas of the CNS from virus-induced pathology.

Author List

Drescher KM, Murray PD, David CS, Pease LR, Rodriguez M

Author

Paul D. Harker-Murray MD, PhD Professor in the Pediatrics department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Animals
Antibodies, Viral
Brain Stem
Cardiovirus Infections
Central Nervous System
Cerebellum
Cerebral Cortex
Corpus Callosum
Corpus Striatum
Cytopathogenic Effect, Viral
Histocompatibility Antigens Class I
Immune System
Immunohistochemistry
Mice
Mice, Inbred C57BL
Mice, Knockout
T-Lymphocyte Subsets
Theilovirus