Author/Authors :
Cognet، نويسنده , , Céline and Farnarier، نويسنده , , Catherine and Gauthier، نويسنده , , Laurent and Frassati، نويسنده , , Coralie and André، نويسنده , , Pascale and Magérus-Chatinet، نويسنده , , Aude and Anfossi، نويسنده , , Nicolas and Rieux-Laucat، نويسنده , , Frederic and Vivier، نويسنده , , Eric and Schleinitz، نويسنده , , Nicolas، نويسنده ,
Abstract :
Killer Ig-like receptors (KIRs) are MHC class I-specific receptors expressed by Natural Killer (NK) and T cell subsets. KIRs either inhibit (KIR-L) or activate (KIR-S) lymphocyte functions. Inhibitory KIR2DL1 and activating KIR2DS1 share ligand specificity for the HLA-C2 group, consistent with their almost identical extracytoplasmic domain. This homology hampered the distinction between KIR2DL1 and KIR2DS1. We report here the characterization of the KIR2DS1+ subsets among primary human NK and T cells. Regardless of the host HLA-C genotype, around 10% of circulating NK cells expressed KIR2DS1 in absence of KIR2DL1. In HLA-C2 individuals, KIR2DS1 was not able to induce NK cell education (i.e., the acquisition of NK cell competence) nor to interfere with KIR2DL1-induced NK cell education. KIR2DS1 was also present on rare oligoclonal TCRαβ+CD8α+ and TCRαβ+CD4−CD8− subsets. As KIR2DS1 has been associated with autoimmunity and hematopoietic stem cell transplantation, these results pave the way to dissect the function of KIR2DS1 in these clinical conditions.
Keywords :
KIRs , NK cells , 2DS1 , KIR+T cells , 2DL1