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扩展杀伤性免疫球蛋白样受体功能:从 HLA Ⅰ类分子识别到微生物产物传感器。

Extending killer Ig-like receptor function: from HLA class I recognition to sensors of microbial products.

机构信息

Department of Experimental Medicine and Center of Excellence for Biomedical Research, University of Genova, Italy.

出版信息

Trends Immunol. 2010 Aug;31(8):289-94. doi: 10.1016/j.it.2010.05.007. Epub 2010 Jul 12.

Abstract

Killer Ig-like receptors (KIRs) are human natural killer (NK) receptors that recognize allotypic determinants of human leukocyte antigen (HLA) class I. Inhibitory KIRs discriminate normal cells from tumour or virus-infected cells that have lost or reduced HLA class I expression. Donor NK cell "alloeffector" responses are exploited in haploidentical haematopoietic stem cell transplantation to treat leukaemia. NK cells also express several toll-like receptors (TLRs) that increase NK cell cytotoxicity and cytokine release in response to ligands. Surprisingly, KIR3DL2 binds the TLR ligand CpG-oligodexynucleotides, and together, they are co-internalized and translocated to TLR9-rich early endosomes. This novel KIR-associated function offers clues to understanding the NK cell response to microbial infection, and extends the role played by KIRs in immune defence.

摘要

杀伤细胞免疫球蛋白样受体(KIRs)是人类自然杀伤(NK)细胞受体,可识别人类白细胞抗原(HLA)I 类的同种异型决定簇。抑制性 KIR 可区分正常细胞与失去或减少 HLA I 类表达的肿瘤或病毒感染细胞。在单倍体相合造血干细胞移植中利用供体 NK 细胞“同种异体效应物”反应来治疗白血病。NK 细胞还表达几种 Toll 样受体(TLRs),这些受体在配体的作用下增加 NK 细胞的细胞毒性和细胞因子释放。令人惊讶的是,KIR3DL2 结合 TLR 配体 CpG-寡脱氧核苷酸,它们一起被共内化并转运到富含 TLR9 的早期内体。这种新的 KIR 相关功能为理解 NK 细胞对微生物感染的反应提供了线索,并扩展了 KIR 在免疫防御中的作用。

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