AI Article Synopsis

  • * This study reveals that the viral gene m138 is responsible for causing the rapid loss of the costimulatory molecule B7-1 (CD80) from the surface of DC, impacting their ability to activate CD8+ T cells.
  • * The research findings indicate that m138 interferes with the secretory pathway of B7-1 by redirecting it to specific compartments, marking the first time a viral protein has been shown to target B7-1 in MCMV infections.

Article Abstract

Murine CMV (MCMV), a beta-herpesvirus, infects dendritic cells (DC) and impairs their function. The underlying events are poorly described. In this study, we identify MCMV m138 as the viral gene responsible for promoting the rapid disappearance of the costimulatory molecule B7-1 (CD80) from the cell surface of DC. This was unexpected, as m138 was previously identified as fcr-1, a putative virus-encoded FcR. m138 impaired the ability of DC to activate CD8+ T cells. Biochemical analysis and immunocytochemistry showed that m138 targets B7-1 in the secretory pathway and reroutes it to lysosomal associated membrane glycoprotein-1+ compartments. These results show a novel function for m138 in MCMV infection and identify the first viral protein to target B7-1.

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http://dx.doi.org/10.4049/jimmunol.177.12.8422DOI Listing

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