4.6 Article

CD4 T-cell Subsets and Tumor Immunity: The Helpful and the Not-so-Helpful

期刊

CANCER IMMUNOLOGY RESEARCH
卷 2, 期 2, 页码 91-98

出版社

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/2326-6066.CIR-13-0216

关键词

-

资金

  1. National Institutes of Health [AI37562, AI48125]
  2. LeRoy Schecter Research Foundation [CA70083]
  3. Arthritis National Research Foundation

向作者/读者索取更多资源

Research over the past decade has revealed the increasingly complex biologic features of the CD4(+) T-cell lineage. This T-cell subset, which was originally defined on the basis of helper activity in antibody responses, expresses receptors that recognize peptides that have been processed and presented by specialized antigen-presenting cells. At the core of the adaptive immune response, CD4 T cells display a large degree of plasticity and the ability to differentiate into multiple sublineages in response to developmental and environmental cues. These differentiated sublineages can orchestrate a broad range of effector activities during the initiation, expansion, and memory phase of an immune response. The contribution of CD4 cells to host defense against pathogenic invasion and regulation of autoimmunity is now well established. Emerging evidence suggests that CD4 cells also actively participate in shaping antitumor immunity. Here, we outline the biologic properties of CD4 T-cell subsets with an emphasis on their contribution to the antitumor response. (C) 2014 AACR.

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

4.6
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