Differential Expression of Ly6C and T-bet Distinguish Effector and Memory Th1 CD4 + Cell Properties during Viral Infection
CD4 + T cells differentiate into multiple effector types, but it is unclear how they form memory T cells during infection in vivo. Profiling virus-specific CD4 + T cells revealed that effector cells with T helper 1 (Th1) or T follicular helper (Tfh) cell characteristics differentiated into memory ce...
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Published in | Immunity (Cambridge, Mass.) Vol. 35; no. 4; pp. 633 - 646 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
28.10.2011
Elsevier Limited |
Subjects | |
Online Access | Get full text |
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Summary: | CD4
+ T cells differentiate into multiple effector types, but it is unclear how they form memory T cells during infection in vivo. Profiling virus-specific CD4
+ T cells revealed that effector cells with T helper 1 (Th1) or T follicular helper (Tfh) cell characteristics differentiated into memory cells, although expression of Tfh cell markers declined over time. In contrast to virus-specific effector CD8
+ T cells, increased IL-7R expression was not a reliable marker of CD4
+ memory precursor cells. However, decreased Ly6C and T-bet (
Tbx21) expression distinguished a subset of Th1 cells that displayed greater longevity and proliferative responses to secondary infection. Moreover, the gene expression profile of Ly6C
loT-bet
int Th1 effector cells was virtually identical to mature memory CD4
+ T cells, indicating early maturation of memory CD4
+ T cell features in this subset during acute viral infection. This study provides a framework for memory CD4
+ T cell development after acute viral infection.
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► Increased IL-7R expression does not mark CD4
+ memory precursor cells ► T-bet acts in a graded manner to regulate formation of Th1 and Tfh cell subsets ► Ly6C
loT-bet
int Th1 effector CD4
+ cells have enhanced longevity and recall responses ► Ly6C
loT-bet
int Th1 effector and memory CD4
+ cells share similar gene expression |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors contributed equally to this work |
ISSN: | 1074-7613 1097-4180 |
DOI: | 10.1016/j.immuni.2011.08.016 |