| Literature DB >> 23345329 |
Tianxiang Zhang1, Jeannine M Scott, Ilwoong Hwang, Sungjin Kim.
Abstract
Because NK cells lack gene-recombination machinery and are thought to be relatively short-lived, it is unclear whether NK cells can mount long-term effective recall responses to reinfections by diverse pathogens. In this article, we report that FcRγ-deficient NK cells, which we recently identified and termed g(-)NK cells, possess distinct memory features directed by FcR-mediated Ab-dependent target recognition. The presence of g(-)NK cells was associated with prior human CMV (HMCV) infection, yet g(-)NK cell responses were not restricted to HCMV-infected target cells. In the presence of virus-specific Abs, g(-)NK cells had greatly enhanced functional capabilities, superior to conventional NK cells, and were highly responsive to cells infected with either HCMV or HSV-1. Remarkably, the g(-)NK cell subset persisted long-term at nearly constant levels in healthy individuals. Therefore, FcRγ deficiency distinguishes an Ab-dependent memory-like NK cell subset with enhanced potential for broad antiviral responses.Entities:
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Year: 2013 PMID: 23345329 PMCID: PMC3623944 DOI: 10.4049/jimmunol.1203034
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422