Ibegbu Chris C, Xu Yong-Xian, Harris Wayne, Maggio David, Miller Joseph D, Kourtis Athena P
Center for AIDS Research, Immunology Core Laboratory, Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30329, USA.
J Immunol. 2005 May 15;174(10):6088-94. doi: 10.4049/jimmunol.174.10.6088.
Killer cell lectin-like receptor G1 (KLRG1) is one of several inhibitory killer cell lectin-like receptors expressed by NK cells and T lymphocytes, mainly CD8(+) effector/memory cells that can secrete cytokines but have poor proliferative capacity. Using multiparameter flow cytometry, we studied KLRG1 expression on CD8(+) T cells specific for epitopes of CMV, EBV, influenza, and HIV. Over 92% of CD8(+) cells specific for CMV or EBV expressed KLRG1 during the latent stage of these chronic infections. CD8(+) T cell cells specific for HIV epitopes were mostly (72-89%) KLRG1(+), even though not quite at the level of predominance noted with CMV or EBV. Lower frequency of KLRG1 expression was observed among CD8(+) cells specific for influenza (40-73%), a resolved infection without a latent stage. We further observed that CD8(+) cells expressing CD57, a marker of replicative senescence, also expressed KLRG1; however, a population of CD57(-)KLRG1(+) cells was also identified. This population may represent a "memory" phenotype, because they also expressed CD27, CD28, CCR7, and CD127. In contrast, CD57(+)KLRG1(+) cells did not express CD27, CD28, and CCR7, and expressed CD127 at a much lower frequency, indicating that they represent effector cells that are truly terminally differentiated. The combination of KLRG1 and CD57 expression might thus aid in refining functional characterization of CD8(+) T cell subsets.
杀伤细胞凝集素样受体G1(KLRG1)是自然杀伤细胞(NK细胞)和T淋巴细胞表达的几种抑制性杀伤细胞凝集素样受体之一,主要由CD8(+)效应/记忆细胞表达,这些细胞可分泌细胞因子,但增殖能力较差。我们使用多参数流式细胞术研究了KLRG1在针对巨细胞病毒(CMV)、EB病毒(EBV)、流感病毒和人类免疫缺陷病毒(HIV)表位的CD8(+) T细胞上的表达。在这些慢性感染的潜伏阶段,超过92%针对CMV或EBV的CD8(+)细胞表达KLRG1。针对HIV表位的CD8(+) T细胞大多(72 - 89%)表达KLRG1,尽管其优势程度不如CMV或EBV。在针对流感病毒(一种无潜伏阶段的已解决感染)的CD8(+)细胞中,观察到KLRG1表达频率较低(40 - 73%)。我们进一步观察到,表达复制性衰老标志物CD57的CD8(+)细胞也表达KLRG1;然而,也鉴定出了一群CD57(-)KLRG1(+)细胞。这群细胞可能代表一种“记忆”表型,因为它们也表达CD27、CD28、CCR7和CD127。相比之下,CD57(+)KLRG1(+)细胞不表达CD27、CD28和CCR7,且表达CD127的频率低得多,表明它们代表真正终末分化的效应细胞。因此,KLRG1和CD57表达的组合可能有助于细化CD8(+) T细胞亚群的功能特征。