| Literature DB >> 25567678 |
Susan Johnson1, Andreas Bergthaler2, Frederik Graw3, Lukas Flatz4, Weldy V Bonilla5, Claire-Anne Siegrist1, Paul-Henri Lambert1, Roland R Regoes6, Daniel D Pinschewer7.
Abstract
Specific CD8(+) T cells (CTLs) play an important role in resolving protracted infection with hepatitis B and C virus in humans and lymphocytic choriomeningitis virus (LCMV) in mice. The contribution of individual CTL specificities to chronic virus control, as well as epitope-specific patterns in timing and persistence of antiviral selection pressure, remain, however, incompletely defined. To monitor and characterize the antiviral efficacy of individual CTL specificities throughout the course of chronic infection, we coinoculated mice with a mixture of wild-type LCMV and genetically engineered CTL epitope-deficient mutant virus. A quantitative longitudinal assessment of viral competition revealed that mice continuously exerted CTL selection pressure on the persisting virus population. The timing of selection pressure characterized individual epitope specificities, and its magnitude varied considerably between individual mice. This longitudinal assessment of "antiviral efficacy" provides a novel parameter to characterize CTL responses in chronic viral infection. It demonstrates remarkable perseverance of all antiviral CTL specificities studied, thus raising hope for therapeutic vaccination in the treatment of persistent viral diseases.Entities:
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Year: 2015 PMID: 25567678 PMCID: PMC4323683 DOI: 10.4049/jimmunol.1401771
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422