Tracking KLRC2 (NKG2C)+ memory-like NK cells in SIV plus and rhCMV plus rhesus macaques

被引:36
作者
Ram, Daniel R. [1 ]
Manickam, Cordelia [1 ]
Hueber, Brady [1 ]
Itell, Hannah L. [2 ]
Permar, Sallie R. [2 ]
Varner, Valerie [1 ]
Reeves, R. Keith [1 ,3 ,4 ]
机构
[1] Harvard Med Sch, Beth Israel Deaconess Med Ctr, CVVR, Boston, MA 02115 USA
[2] Duke Univ, Med Ctr, Human Vaccine Inst, Durham, NC 27706 USA
[3] MIT, Gen Hosp, Ragon Inst Massachusetts, Cambridge, MA 02139 USA
[4] Harvard, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
NATURAL-KILLER-CELLS; HUMAN CYTOMEGALOVIRUS-INFECTION; ADAPTIVE IMMUNITY; T-CELL; ANTIGEN; VIRUS; TRANSPLANTATION; EXPRESSION; CD94/NKG2; RECEPTORS;
D O I
10.1371/journal.ppat.1007104
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Natural killer (NK) cells classically typify the nonspecific effector arm of the innate immune system, but have recently been shown to possess memory-like properties against multiple viral infections, most notably CMV. Expression of the activating receptor NKG2C is elevated on human NK cells in response to infection with CMV as well as HIV, and may delineate cells with memory and memory-like functions. A better understanding of how NKG2C+ NK cells specifically respond to these pathogens could be significantly advanced using nonhuman primate (NHP) models but, to date, it has not been possible to distinguish NKG2C from its inhibitory counterpart, NKG2A, in NHP because of unfaithful antibody cross-reactivity. Using novel RNA-based flow cytometry, we identify for the first time true memory NKG2C+ NK cells in NHP by gene expression (KLRC2), and show that these cells have elevated frequencies and diversify their functional repertoire specifically in response to rhCMV and SIV infections.
引用
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页数:14
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