CD94 functions as a natural killer cell inhibitory receptor for different HLA class I alleles: Identification of the inhibitory form of CD94 by the use of novel monoclonal antibodies

被引:140
作者
Sivori, S
Vitale, M
Bottino, C
Marcenaro, E
Sanseverino, L
Parolini, S
Moretta, L
Moretta, A
机构
[1] IST SCI STUDIO & CURA TUMORI, IMMUNOPATOL LAB, I-16132 GENOA, ITALY
[2] CTR BIOTECNOL AVANZATE, I-16132 GENOA, ITALY
[3] UNIV GENOA, IST ISTOL & EMBRIOL GEN, GENOA, ITALY
[4] UNIV GENOA, IST PATOL GEN, GENOA, ITALY
[5] UNIV BRESCIA, DIPARTIMENTO SCI BIOMED & BIOTECNOL, BRESCIA, ITALY
关键词
natural killer cell receptor; CD94; cytotoxicity;
D O I
10.1002/eji.1830261032
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD94 molecules have been suggested to function as inhibitory natural killer cell (NK) receptors involved in the recognition of HLA-B alleles sharing the Bw6 supertypic specificity. In this study, we show that CD94 molecules may play a more general role: they are also involved in the recognition of other HLA class I molecules, including HLA-C and at least some HLA-A alleles. The inhibitory effect mediated by CD94 molecules on NK cytolytic activity is lower in magnitude than that of bona fide inhibitory receptors such as p58 or p70. Distinct from the other human NK receptors involved in HLA class I recognition, CD94 is expressed on virtually all NK cells. In addition, it has been shown to be functionally heterogeneous since, in different clones, CD94 mediated either cell triggering or inhibition. Although NK cells expressing inhibitory CD94 molecules are usually characterized by a CD94(bright) phenotype, there is no precise correlation between fluorescence intensity and inhibitory or activating function. Here, we describe two novel monoclonal antibodies (mAb) which selectively recognize inhibitory CD94 molecules and bind to a subset (variable in size among different donors) of CD94(bright) cells. The use of these mAb allows the direct assessment of NK cells expressing inhibitory CD94 receptors both at the population and at the clonal level.
引用
收藏
页码:2487 / 2492
页数:6
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