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自然杀伤细胞肿瘤坏死因子相关凋亡诱导配体在体内清除未成熟树突状细胞并限制树突状细胞疫苗接种效果。

NK cell TRAIL eliminates immature dendritic cells in vivo and limits dendritic cell vaccination efficacy.

作者信息

Hayakawa Yoshihiro, Screpanti Valentina, Yagita Hideo, Grandien Alf, Ljunggren Hans-Gustaf, Smyth Mark J, Chambers Benedict J

机构信息

Cancer Immunology Program, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia.

出版信息

J Immunol. 2004 Jan 1;172(1):123-9. doi: 10.4049/jimmunol.172.1.123.

Abstract

Recent studies have implicated a possible role for NK cells in regulating dendritic cells (DC) in vitro. In the present study, we demonstrate that immature DC are rapidly eliminated by NK cells in vivo via a pathway dependent on the TNF-related apoptosis-inducing ligand (TRAIL). Elimination of NK cells and/or neutralization of TRAIL function during immunization with immature DC loaded with nonself or tumor Ags significantly enhanced T cell responses to these Ags and Ag-specific tumor immunity. These data suggested that NK cell TRAIL might regulate responses to vaccination by controlling the survival of Ag-loaded DC.

摘要

近期研究表明,自然杀伤细胞(NK细胞)在体外调节树突状细胞(DC)方面可能发挥作用。在本研究中,我们证明未成熟DC在体内会通过依赖肿瘤坏死因子相关凋亡诱导配体(TRAIL)的途径被NK细胞迅速清除。在用负载非自身或肿瘤抗原的未成熟DC进行免疫接种期间,清除NK细胞和/或中和TRAIL功能可显著增强T细胞对这些抗原的反应以及抗原特异性肿瘤免疫。这些数据表明,NK细胞TRAIL可能通过控制负载抗原的DC的存活来调节对疫苗接种的反应。

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