Sim Malcolm J W, Li Beining, Long Eric O
Centre for Immuno-Oncology, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7DQ, United Kingdom.
Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, 20852, United States of America.
Oxf Open Immunol. 2025 Apr 17;6(1):iqaf003. doi: 10.1093/oxfimm/iqaf003. eCollection 2025.
Class I and II human leukocyte antigens (HLA-I and HLA-II) present peptide antigens for immunosurveillance by T cells. HLA molecules also form ligands for a plethora of innate, germline-encoded receptors. Many of these receptors engage HLA molecules in a peptide sequence independent manner, with binding sites outside the peptide binding groove. However, some receptors, typically expressed on natural killer (NK) cells, engage the HLA presented peptide directly. Remarkably, some of these receptors display exquisite specificity for peptide sequences, with the capacity to detect sequences conserved in pathogens. Here, we review evidence for peptide-specific NK cell receptors (PSNKRs) and discuss their potential roles in immunity.
I类和II类人类白细胞抗原(HLA-I和HLA-II)呈递肽抗原以供T细胞进行免疫监视。HLA分子还形成了众多先天的、种系编码受体的配体。这些受体中的许多以不依赖肽序列的方式与HLA分子结合,其结合位点位于肽结合槽之外。然而,一些通常在自然杀伤(NK)细胞上表达的受体则直接与HLA呈递的肽结合。值得注意的是,其中一些受体对肽序列表现出极高的特异性,能够检测病原体中保守的序列。在此,我们综述了肽特异性NK细胞受体(PSNKRs)的相关证据,并讨论它们在免疫中的潜在作用。