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IL-21-producer CD4+ T cell kinetics during primary simian immunodeficiency virus infection.

Abstract
IL-21 signaling is important for T cell and B cell-mediated clearance of chronic viral infections. While non-cognate follicular helper CD4+ T cells (TFH) are indicated to be pivotal in providing IL-21-mediated help to activated B cells within germinal centers, how this signaling may be disrupted in early AIDS virus infection is not clear. In this study, we assessed the lineage and kinetics of peripheral blood IL-21-producing CD4+ T cells in primary simian immunodeficiency virus (SIV) infection of rhesus macaques. After SIV challenge, antigen-nonspecific IL-21 production was observed in Th1, Th2 and Th17 cells with Th1 dominance. While IL-21+ Th2 and IL-21+ Th17 showed variable kinetics, an increase in total IL-21+ CD4+ T cells and IL-21+ Th1 from week 3 to week 8 was observed, preceding plasma SIV-specific IgG development from week 5 to week 12. SIV Gag-specific IL-21+ CD4+ T cells detectable at week 2 were decreased in frequencies at week 5. Results imply that kinetics of IL-21+ CD4+ T cells comprised of multiple lineages, potentially targeted by SIV with a bias of existing frequencies during their precursor stage, associate with availability of cooperative B-cell help provided through a proportionate precursor pool developing into TFH and subsequent anti-SIV antibody responses.
AuthorsShoi Shi, Sayuri Seki, Tetsuro Matano, Hiroyuki Yamamoto
JournalMicrobes and infection (Microbes Infect) 2013 Sep-Oct Vol. 15 Issue 10-11 Pg. 697-707 ISSN: 1769-714X [Electronic] France
PMID23791954 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2013 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.
Chemical References
  • Interleukins
  • interleukin-21
Topics
  • Animals
  • CD4-Positive T-Lymphocytes (immunology)
  • Interleukins (metabolism)
  • Macaca mulatta
  • Simian Acquired Immunodeficiency Syndrome (immunology)
  • Simian Immunodeficiency Virus (immunology)
  • T-Lymphocyte Subsets (immunology)
  • Time Factors

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