Burster Timo, Gärtner Fabian, Bulach Christiane, Zhanapiya Anuar, Gihring Adrian, Knippschild Uwe
Department of Biology, School of Sciences and Humanities, Nazarbayev University, Kabanbay Batyr Ave. 53, 010000 Nur-Sultan, Kazakhstan.
Department of General and Visceral Surgery, Surgery Center, Ulm University Hospital, Albert-Einstein-Allee 23, 89081 Ulm, Germany.
Pharmaceuticals (Basel). 2021 Mar 8;14(3):236. doi: 10.3390/ph14030236.
Immunotherapy has been established as an important area in the therapy of malignant diseases. Immunogenicity sufficient for immune recognition and subsequent elimination can be bypassed by tumors through altered and/or reduced expression levels of major histocompatibility complex class I (MHC I) molecules. Natural killer (NK) cells can eliminate tumor cells in a MHC I antigen presentation-independent manner by an array of activating and inhibitory receptors, which are promising candidates for immunotherapy. Here we summarize the latest findings in recognizing and regulating MHC I molecules that affect NK cell surveillance of glioblastoma cells.
免疫疗法已成为恶性疾病治疗中的一个重要领域。肿瘤可通过改变和/或降低主要组织相容性复合体I类(MHC I)分子的表达水平,绕过足以进行免疫识别和后续清除的免疫原性。自然杀伤(NK)细胞可通过一系列激活和抑制性受体,以不依赖MHC I抗原呈递的方式消除肿瘤细胞,这些受体是免疫疗法很有前景的候选对象。在此,我们总结了在识别和调节影响NK细胞对胶质母细胞瘤细胞监测的MHC I分子方面的最新发现。