Document Detail


Signaling pathways in T follicular helper cells.
MedLine Citation:
PMID:  20525897     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Th cell functional subsets have unique transcriptional programs that form the molecular basis for T cell differentiation and functions. T follicular helper (TFH) cells have emerged as the main providers of T cell help to B cells during the germinal center (GC) reaction, where B cells undergo selection events through competition for Ag and for access to GC T cell-mediated prosurvival and differentiation signals. Because T cell help is one limiting factor for GC B cells, the molecular mechanisms controlling TFH cell abundance and functionality are central to the GC reaction and generation of long-term humoral immunity. Two signaling pathways are absolutely critical for TFH cells: phosphoinositide-3 kinase pathway and the signaling lymphocyte activation molecule-associated protein. In this review, the molecular mechanisms constituting the signaling network in TFH cells will be explored.
Authors:
Julia Rolf; Kirsten Fairfax; Martin Turner
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review    
Journal Detail:
Title:  Journal of immunology (Baltimore, Md. : 1950)     Volume:  184     ISSN:  1550-6606     ISO Abbreviation:  J. Immunol.     Publication Date:  2010 Jun 
Date Detail:
Created Date:  2010-06-07     Completed Date:  2010-06-18     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  2985117R     Medline TA:  J Immunol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  6563-8     Citation Subset:  AIM; IM    
Affiliation:
Laboratory of Lymphocyte Signalling and Development, Babraham Institute, Cambridge, United Kingdom.
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MeSH Terms
Descriptor/Qualifier:
Animals
Germinal Center / immunology*
Humans
Lymphocyte Activation / immunology
Signal Transduction / immunology*
T-Lymphocyte Subsets / immunology*
T-Lymphocytes, Helper-Inducer / immunology*
Grant Support
ID/Acronym/Agency:
//Biotechnology and Biological Sciences Research Council; //Medical Research Council

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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