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Cell fate decision: T-helper 1 and 2 subsets in immune responses

After activation CD4(+) helper T cells differentiate into T-helper (Th) 1 or Th2 effector cells. These two subsets are characterized by their distinct cytokine expression pattern and the immune function they mediate. Over the past years, a number of factors have been identified to affect helper T ce...

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Detalles Bibliográficos
Autores principales: Dong, Chen, Flavell, Richard A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC130000/
https://www.ncbi.nlm.nih.gov/pubmed/11094427
http://dx.doi.org/10.1186/ar85
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author Dong, Chen
Flavell, Richard A
author_facet Dong, Chen
Flavell, Richard A
author_sort Dong, Chen
collection PubMed
description After activation CD4(+) helper T cells differentiate into T-helper (Th) 1 or Th2 effector cells. These two subsets are characterized by their distinct cytokine expression pattern and the immune function they mediate. Over the past years, a number of factors have been identified to affect helper T cell lineage determination, including antigen receptor, coreceptors and, most importantly, cytokine environment. In this review, we also summarize recent advancement in understanding of transcriptional and signaling regulation of the differentiation process. This knowledge will become important in the future to develop means in treating immune disorders.
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spelling pubmed-1300002002-10-28 Cell fate decision: T-helper 1 and 2 subsets in immune responses Dong, Chen Flavell, Richard A Arthritis Res Review After activation CD4(+) helper T cells differentiate into T-helper (Th) 1 or Th2 effector cells. These two subsets are characterized by their distinct cytokine expression pattern and the immune function they mediate. Over the past years, a number of factors have been identified to affect helper T cell lineage determination, including antigen receptor, coreceptors and, most importantly, cytokine environment. In this review, we also summarize recent advancement in understanding of transcriptional and signaling regulation of the differentiation process. This knowledge will become important in the future to develop means in treating immune disorders. BioMed Central 2000 2000-03-27 /pmc/articles/PMC130000/ /pubmed/11094427 http://dx.doi.org/10.1186/ar85 Text en Copyright © 2000 Current Science Ltd
spellingShingle Review
Dong, Chen
Flavell, Richard A
Cell fate decision: T-helper 1 and 2 subsets in immune responses
title Cell fate decision: T-helper 1 and 2 subsets in immune responses
title_full Cell fate decision: T-helper 1 and 2 subsets in immune responses
title_fullStr Cell fate decision: T-helper 1 and 2 subsets in immune responses
title_full_unstemmed Cell fate decision: T-helper 1 and 2 subsets in immune responses
title_short Cell fate decision: T-helper 1 and 2 subsets in immune responses
title_sort cell fate decision: t-helper 1 and 2 subsets in immune responses
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC130000/
https://www.ncbi.nlm.nih.gov/pubmed/11094427
http://dx.doi.org/10.1186/ar85
work_keys_str_mv AT dongchen cellfatedecisionthelper1and2subsetsinimmuneresponses
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