利用自然杀伤细胞介导的先天免疫反应治疗癌症:进展和挑战

Anil Kumar, Adeleh Taghi Khani, S. Swaminathan
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引用次数: 2

摘要

抗原-1等)和来自异常细胞和微环境的抑制信号(NKG2A、杀伤细胞凝集素样受体G1、带有免疫球蛋白和ITIM结构域的t细胞免疫受体(TIGIT)等)。7除激活和抑制受体外,共刺激受体或粘附分子(2B4、CD27、CD28、CD226等)8-11也能诱导NK细胞功能。NK细胞通过肿瘤坏死因子(tumor necrosis factor, TNF)相关的凋亡诱导配体和Fas配体,直接释放穿孔素、颗粒酶- b等溶解颗粒,诱导靶细胞凋亡。12,13 nk介导的另一种杀伤机制是抗体依赖性的
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Harnessing Natural Killer Cell-Mediated Innate Immune Responses for Cancer Treatment: Advances and Challenges

Harnessing Natural Killer Cell-Mediated Innate Immune Responses for Cancer Treatment: Advances and Challenges
antigen-1, etc .) and inhibitory signals (NKG2A, killer cell lectin-like receptor G1, and T-cell immunoreceptor with immunoglobulin and ITIM domain (TIGIT), etc .) that originate from abnormal cells and the microenvironment. 7 In addition to activating and inhibitory receptors, co-stimulatory receptors or adhesion molecules (2B4, CD27, CD28, CD226 etc .) 8–11 can induce NK cell function. NK cells induce apoptosis of the target cell via tumor necrosis factor (TNF)- related apoptosis-inducing ligand and Fas ligand, and by directly releasing lytic granules such as perforin and granzyme-B. 12,13 Another mechanism of NK-mediated killing is antibody-dependent
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