Artigo Revisado por pares

Down-regulation of the NKG2D ligand MICA by the human cytomegalovirus glycoprotein UL142

2006; Elsevier BV; Volume: 346; Issue: 1 Linguagem: Inglês

10.1016/j.bbrc.2006.05.092

ISSN

1090-2104

Autores

N. Jan Chalupny, Annie Rein‐Weston, Stephanie Dosch, David Cosman,

Tópico(s)

T-cell and B-cell Immunology

Resumo

Human cytomegalovirus (HCMV) employs a variety of strategies to modify or evade the host immune response, and natural killer (NK) cells play a crucial role in controlling cytomegalovirus infections in mice and humans. Activation of NK cells through the receptor NKG2D/DAP10 leads to killing of NKG2D ligand-expressing cells. We have previously shown that HCMV is able to down-regulate the surface expression of some NKG2D ligands, ULBP1, ULBP2, and MICB via the viral glycoprotein UL16. Here, we show that the viral gene product UL142 is able to down-regulate another NKG2D ligand, MICA, leading to protection from NK cytotoxicity. UL142 is not able to affect surface expression of all MICA alleles, however, which may reflect selective pressure on the host to thwart viral immune evasion, further supporting an important role for the MICA–NKG2D interaction in immune surveillance.

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