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

被引:300
作者
Hale, J. Scott [1 ,2 ,3 ]
Youngblood, Ben [1 ,2 ,3 ]
Latner, Donald R. [1 ,2 ]
Mohammed, Ata Ur Rasheed [1 ,2 ]
Ye, Lilin [1 ,2 ]
Akondy, Rama S. [1 ,2 ]
Wu, Tuoqi [1 ,2 ]
Iyer, Smita S. [1 ,2 ]
Ahmed, Rafi [1 ,2 ,3 ]
机构
[1] Emory Univ, Sch Med, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Ctr HIV AIDS Vaccine Immunol & Immunogen Discover, Atlanta, GA 30322 USA
关键词
CXC CHEMOKINE RECEPTOR-5; EXPRESSION; BCL6; VACCINES; VACCINOLOGY; ACTIVATION; MECHANISMS; EFFECTOR; BLIMP-1; IL-21;
D O I
10.1016/j.immuni.2013.02.020
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
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.
引用
收藏
页码:805 / 817
页数:13
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