Peptide antagonism as a mechanism for NK cell activation

被引:130
作者
Fadda, Lena [1 ]
Borhis, Gwenoline [1 ]
Ahmed, Parvin [1 ]
Cheent, Kuldeep [1 ]
Pageon, Sophie V. [2 ]
Cazaly, Angelica [3 ]
Stathopoulos, Stavros [1 ]
Middleton, Derek [4 ,5 ]
Mulder, Arend [6 ]
Claas, Frans H. J. [6 ]
Elliott, Tim [3 ]
Davis, Daniel M. [2 ]
Purbhoo, Marco A. [1 ]
Khakoo, Salim I. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Div Med, London W2 1PG, England
[2] Univ London Imperial Coll Sci Technol & Med, Div Cell & Mol Med, London W2 1PG, England
[3] Univ Southampton, Southampton Gen Hosp, Canc Sci Div, Southampton SO16 6YD, Hants, England
[4] Royal Liverpool Univ Hosp, Liverpool L7 8XP, Merseyside, England
[5] Univ Liverpool, Sch Infect & Immun, Liverpool L7 8XP, Merseyside, England
[6] Leiden Univ, Med Ctr, Dept Immunohaematol & Blood Transfus, NL-2300 RC Leiden, Netherlands
基金
英国医学研究理事会; 英国惠康基金;
关键词
killer cell immunoglobulin-like receptors; MHC class I; MHC CLASS-I; INHIBITORY RECEPTOR GENES; IMMUNOGLOBULIN-LIKE RECEPTOR; C VIRUS-INFECTION; COMPLEX CLASS-I; HLA CLASS-I; MEDIATED LYSIS; DIRECT BINDING; CUTTING EDGE; RECOGNITION;
D O I
10.1073/pnas.0913745107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Inhibition of natural killer (NK) cells is mediated by MHC class I receptors including the killer cell Ig-like receptor (KIR). We demonstrate that HLA-C binding peptides can function as altered peptide ligands for KIR and antagonize the inhibition mediated by KIR2DL2/KIR2DL3. Antagonistic peptides promote clustering of KIR at the interface of effector and target cells, but do not result in inhibition of NK cells. Our data show that, as for T cells, small changes in the peptide content of MHC class I can regulate NK cell activity.
引用
收藏
页码:10160 / 10165
页数:6
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