4.2 Article

Therapeutic potential of FOXP3+ regulatory T cells and their interactions with dendritic cells

期刊

HUMAN IMMUNOLOGY
卷 70, 期 5, 页码 294-299

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.humimm.2009.02.007

关键词

FOXP3; Tregs; Tolerance; Autoimmunity; Dendritic cells; LRRC32; GARP; TGFbeta; Latency associated peptide

向作者/读者索取更多资源

FOXP3(+) regulatory T cells, a unique subset of T cells, are critical for orchestrating an immune response and preventing Self-reactivity. With) the increasing prevalence and unsatisfactory treatment of autoimmunity, allergic diseases, cancer and chronic infections, much attention has been focused on understanding their mechanisms of action in order to manipulate their function. One goal is to develop drugs or biologics that can enhance or abrogate their functions. Another approach is to utilize Tregs in adoptive cell-based therapy to treat autoimmune diseases or transplant-related complications. This review will focus on their therapeutic potential and mechanisms of action, particularly their interaction with dendritic cells. Published by Elsevier Inc. on behalf of American Society for Histocompatibility and Immunogenetics.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据