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前沿:CD160 与其 HLA - C 生理配体结合可触发细胞毒性外周血自然杀伤细胞亚群分泌独特的细胞因子谱。

Cutting edge: engagement of CD160 by its HLA-C physiological ligand triggers a unique cytokine profile secretion in the cytotoxic peripheral blood NK cell subset.

作者信息

Barakonyi Aliz, Rabot Magali, Marie-Cardine Anne, Aguerre-Girr Maryse, Polgar Beata, Schiavon Valérie, Bensussan Armand, Le Bouteiller Philippe

机构信息

Institut National de la Santé et de la Recherche Médicale (INSERM) Unité 563, Centre de Physiopathologie Toulouse-Purpan, Toulouse, France.

出版信息

J Immunol. 2004 Nov 1;173(9):5349-54. doi: 10.4049/jimmunol.173.9.5349.

Abstract

CD160 is an Ig-like activating NK cell receptor expressed on the majority of circulating NK cells. This population corresponds to the nonproliferating, highly cytolytic, CD56dimCD16+ subset. CD160 engagement by HLA-C molecules mediates cytotoxic function. In this study, we report that upon specific activation by the physiological ligand HLA-C, or Ab cross-linking, CD160+ peripheral blood NK cells produce IFN-gamma, TNF-alpha, and IL-6. This unique CD160-mediated cytokine production differs from the one observed after CD16 engagement whose expression is also restricted to the CD56dim cytotoxic NK cell subset. As already reported for the CD160-mediated cytotoxic effector function, CD160-mediated cytokine production by peripheral blood-NK cells is negatively controlled by the killer Ig-like receptor CD158b. Thus, the CD160 receptor represents a unique triggering surface molecule expressed by cytotoxic NK cells that participates in the inflammatory response and determines the type of subsequent specific immunity.

摘要

CD160是一种在大多数循环NK细胞上表达的免疫球蛋白样激活型NK细胞受体。这一细胞群体对应于不增殖、高细胞毒性的CD56dimCD16+亚群。HLA-C分子与CD160结合介导细胞毒性功能。在本研究中,我们报告,在被生理性配体HLA-C特异性激活或抗体交联后,CD160+外周血NK细胞会产生γ干扰素、肿瘤坏死因子-α和白细胞介素-6。这种独特的由CD160介导的细胞因子产生不同于CD16结合后观察到的情况,CD16的表达也局限于CD56dim细胞毒性NK细胞亚群。正如已报道的CD160介导的细胞毒性效应功能一样,外周血NK细胞由CD160介导的细胞因子产生受到杀伤细胞免疫球蛋白样受体CD158b的负调控。因此,CD160受体是一种由细胞毒性NK细胞表达的独特触发表面分子,它参与炎症反应并决定后续特异性免疫的类型。

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