| Literature DB >> 22018471 |
Heather D Marshall1, Anmol Chandele, Yong Woo Jung, Hailong Meng, Amanda C Poholek, Ian A Parish, Rachel Rutishauser, Weiguo Cui, Steven H Kleinstein, Joe Craft, Susan M Kaech.
Abstract
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(lo)T-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.Entities:
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Year: 2011 PMID: 22018471 PMCID: PMC3444169 DOI: 10.1016/j.immuni.2011.08.016
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745