Department of Medical Oncology, National Center for Tumor Diseasesm, University Hospital Heidelberg, Heidelberg, Germany.
Clinical Cooperation Unit Applied Tumor Immunity (D120), German Cancer Research Center, Heidelberg, Germany.
Front Immunol. 2018 Oct 17;9:2410. doi: 10.3389/fimmu.2018.02410. eCollection 2018.
Adaptive Natural Killer (NK) cells, a heterogenous subpopulation of human NK cells with a unique phenotypic and functional signature, became arguably one of the central areas of interest in the field. While their existence seems closely associated with prior exposure to human cytomegalovirus (HCMV), many questions regarding their origin and regulation remain unanswered. However, a common denominator for the majority of adaptive NK cells is the expression of the activating heterodimeric receptor CD94/NKG2C that binds to HLA-E, a non-classical HLA molecule, that displays a comparably restricted expression pattern, very limited polymorphism and presents a distinct set of peptides. Recent studies suggest that-in analogy to T cell responses-peptides presented on HLA-E could play an unexpectedly decisive role for the biology of adaptive NK cells. Here, we discuss how this perspective on the CD94/NKG2C-HLA-E axis aligns with the existing literature and speculate about possible translational implication.
适应性自然杀伤 (NK) 细胞是人类 NK 细胞的一个异质性亚群,具有独特的表型和功能特征,可说是该领域的关注重点之一。虽然它们的存在似乎与人类巨细胞病毒 (HCMV) 的先前暴露密切相关,但关于它们的起源和调节的许多问题仍未得到解答。然而,大多数适应性 NK 细胞的共同点是表达激活的异二聚体受体 CD94/NKG2C,该受体与 HLA-E 结合,HLA-E 是一种非经典 HLA 分子,具有相对受限的表达模式、非常有限的多态性,并呈现出独特的肽集合。最近的研究表明,与 T 细胞反应类似,HLA-E 上呈现的肽可能对适应性 NK 细胞的生物学起着出人意料的决定性作用。在这里,我们讨论了这种对 CD94/NKG2C-HLA-E 轴的看法如何与现有文献相一致,并推测了可能的转化意义。