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<https://www.ncbi.nlm.nih.gov/pmc/articles/PMC254260> dc:abstract "C57BL/6 (B6) mice infected with mouse hepatitis virus (MHV) strain JHM develop a clinically evident, demyelinating encephalomyelitis. Infectious virus can be isolated from the spinal cords of these mice and is invariably mutated in the immunodominant CD8 T-cell epitope recognized in this strain. We showed previously that these persistently infected mice did not mount a measurable serum anti-MHV neutralizing antibody response. Here we show that cytotoxic T-lymphocyte (CTL) escape was not detected in MHV-infected BALB/b mice (H-2(b) haplotype), even though the same CD8 T-cell epitopes were recognized as in B6 mice. BALB/b mice had 25-fold more MHV-specific antibody-secreting cells in the central nervous system, the site of infection, than B6 mice, suggesting that local production of anti-MHV antibody contributed to this absence of CTL escape. Additionally, administration of anti-MHV neutralizing antibody to infected B6 mice suppressed the development of CTL escape mutants. These findings indicate a key role for the anti-MHV antibody response in suppressing virus replication, thereby minimizing the emergence and competitive advantage of CTL escape mutants." ;
    dc:creator "['Dandekar, Ajai A.', 'Jacobsen, Gary', 'Waldschmidt, Thomas J.', 'Perlman, Stanley']" ;
    dc:identifier <http://dx.doi.org/10.1128/JVI.77.22.11867-11874.2003>,
        <https://www.ncbi.nlm.nih.gov/pmc/articles/PMC254260> ;
    dc:title "Antibody-Mediated Protection against Cytotoxic T-Cell Escape in Coronavirus-Induced Demyelination" ;
    sso:source_x "PMC" .

