4.8 Article

Distinct Memory CD4+ T Cells with Commitment to T Follicular Helper- and T Helper 1-Cell Lineages Are Generated after Acute Viral Infection

期刊

IMMUNITY
卷 38, 期 4, 页码 805-817

出版社

CELL PRESS
DOI: 10.1016/j.immuni.2013.02.020

关键词

-

资金

  1. NIH [P01 A1080192, RO1 AI030048]
  2. Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery [UM1AI100663]
  3. American Cancer Society (ACS) postdoctoral fellowship [PF-09-134-01-MPC]
  4. National Institute of Allergy and Infectious Diseases Training Grant [T32AI074492, F32 A1096709-01A1]

向作者/读者索取更多资源

CD4(+) T follicular helper (Tfh) cells provide the required signals to B cells for germinal center reactions that are necessary for long-lived antibody responses. However, it remains unclear whether there are CD4(+) memory T cells committed to the Tfh cell lineage after antigen clearance. By using adoptive transfer of antigen-specific memory CD4(+) T cell sub-populations in the lymphocytic choriomeningitis virus infection model, we found that there are distinct memory CD4(+) T cell populations with commitment to either Tfh- or Th1-cell lineages. Our conclusions are based on gene expression profiles, epigenetic studies, and phenotypic and functional analyses. Our findings indicate that CD4(+) memory T cells remember their previous effector lineage after antigen clearance, being poised to reacquire their lineage-specific effector functions upon antigen reencounter. These findings have important implications for rational vaccine design, where improving the generation and engagement of memory Tfh cells could be used to enhance vaccine-induced protective immunity.

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

4.8
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