MCMV glycoprotein gp40 confers virus resistance to CD8+ T cells and NK cells in vivo

A. Krmpotic, D.H. Busch, I. Bubic, F. Gebhardt, H. Hengel, M. Hasan, Tony Scalzo, U.H. Koszinowski, S. Jonjic

Research output: Contribution to journalArticle

161 Citations (Scopus)

Abstract

The susceptibility of certain inbred mouse strains to murine cytomegalovirus (MCMV) is related to their inability to generate a strong natural killer (NK) cell response. We addressed here whether the MCMV susceptibility of the BALB/c strain is due to viral functions that control NK cell activation in a strain-specific manner. MCMV expresses two proteins, gp48 and gp40, that are encoded by the genes m06 and m152, respectively; they down-regulate major histocompatibility complex (MHC) class I expression at the plasma membrane. Using MCMV deletion mutants and revertants, we found that gp40 but not gp48 controls NK cell activation. Absence of gp40 improved antiviral NK cell control in BALB/c, but not C57BL/6, mice. Down-regulation of H-60, the high-affinity ligand for the NKG2D receptor, was the mechanism by which gp40 modulates NK cell activation. Thus, a single herpesvirus protein has a dual function in inhibiting both the adaptive as well as the innate immune response.
Original languageEnglish
Pages (from-to)529-535
JournalNature Immunology
Volume3
DOIs
Publication statusPublished - 2002

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