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在针对恶性肿瘤的免疫治疗中利用树突状细胞和自然杀伤T细胞。

Exploiting dendritic cells and natural killer T cells in immunotherapy against malignancies.

作者信息

Fujii Shin-ichiro

机构信息

Research Unit for Cellular Immunotherapy, Research Center for Allergy and Immunology, The Institute of Physical and Chemical Research, Yokohama RIKEN, 1-7-22, Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, 230-0045 Japan.

出版信息

Trends Immunol. 2008 May;29(5):242-9. doi: 10.1016/j.it.2008.02.002. Epub 2008 Mar 26.

Abstract

A primary focus of tumor immunotherapy research is to change the immune system so that it becomes immunized and not tolerized to the presentation of antigens by or from tumor cells. Dendritic cells (DCs) are the logical target for the development of immunotherapies because DCs instruct the ensuing immune response. Upon activation, invariant natural killer T (iNKT) cells have direct antitumor effects and also induce in situ DC maturation, linking the innate and adaptive arms of the immune system in an immunogenic form. The characterization and manipulation of DC function in tumor-bearing hosts will provide new insights into mechanisms of tumor immunology and lead to the development of successful clinical strategies.

摘要

肿瘤免疫治疗研究的一个主要重点是改变免疫系统,使其对肿瘤细胞呈现的或来自肿瘤细胞的抗原产生免疫反应而非耐受。树突状细胞(DCs)是免疫治疗开发的合理靶点,因为DCs指导后续的免疫反应。激活后,不变自然杀伤T(iNKT)细胞具有直接的抗肿瘤作用,还能诱导原位DC成熟,以免疫原性形式连接免疫系统的固有和适应性分支。对荷瘤宿主中DC功能的表征和调控将为肿瘤免疫学机制提供新的见解,并推动成功临床策略的开发。

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