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CD4(+)T Cells: Differentiation and Functions

CD4(+)T cells are crucial in achieving a regulated effective immune response to pathogens. Naive CD4(+)T cells are activated after interaction with antigen-MHC complex and differentiate into specific subtypes depending mainly on the cytokine milieu of the microenvironment. Besides the classical T-he...

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Detalles Bibliográficos
Autores principales: Luckheeram, Rishi Vishal, Zhou, Rui, Verma, Asha Devi, Xia, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312336/
https://www.ncbi.nlm.nih.gov/pubmed/22474485
http://dx.doi.org/10.1155/2012/925135
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author Luckheeram, Rishi Vishal
Zhou, Rui
Verma, Asha Devi
Xia, Bing
author_facet Luckheeram, Rishi Vishal
Zhou, Rui
Verma, Asha Devi
Xia, Bing
author_sort Luckheeram, Rishi Vishal
collection PubMed
description CD4(+)T cells are crucial in achieving a regulated effective immune response to pathogens. Naive CD4(+)T cells are activated after interaction with antigen-MHC complex and differentiate into specific subtypes depending mainly on the cytokine milieu of the microenvironment. Besides the classical T-helper 1 and T-helper 2, other subsets have been identified, including T-helper 17, regulatory T cell, follicular helper T cell, and T-helper 9, each with a characteristic cytokine profile. For a particular phenotype to be differentiated, a set of cytokine signaling pathways coupled with activation of lineage-specific transcription factors and epigenetic modifications at appropriate genes are required. The effector functions of these cells are mediated by the cytokines secreted by the differentiated cells. This paper will focus on the cytokine-signaling and the network of transcription factors responsible for the differentiation of naive CD4(+)T cells.
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spelling pubmed-33123362012-04-03 CD4(+)T Cells: Differentiation and Functions Luckheeram, Rishi Vishal Zhou, Rui Verma, Asha Devi Xia, Bing Clin Dev Immunol Review Article CD4(+)T cells are crucial in achieving a regulated effective immune response to pathogens. Naive CD4(+)T cells are activated after interaction with antigen-MHC complex and differentiate into specific subtypes depending mainly on the cytokine milieu of the microenvironment. Besides the classical T-helper 1 and T-helper 2, other subsets have been identified, including T-helper 17, regulatory T cell, follicular helper T cell, and T-helper 9, each with a characteristic cytokine profile. For a particular phenotype to be differentiated, a set of cytokine signaling pathways coupled with activation of lineage-specific transcription factors and epigenetic modifications at appropriate genes are required. The effector functions of these cells are mediated by the cytokines secreted by the differentiated cells. This paper will focus on the cytokine-signaling and the network of transcription factors responsible for the differentiation of naive CD4(+)T cells. Hindawi Publishing Corporation 2012 2012-03-14 /pmc/articles/PMC3312336/ /pubmed/22474485 http://dx.doi.org/10.1155/2012/925135 Text en Copyright © 2012 Rishi Vishal Luckheeram et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Luckheeram, Rishi Vishal
Zhou, Rui
Verma, Asha Devi
Xia, Bing
CD4(+)T Cells: Differentiation and Functions
title CD4(+)T Cells: Differentiation and Functions
title_full CD4(+)T Cells: Differentiation and Functions
title_fullStr CD4(+)T Cells: Differentiation and Functions
title_full_unstemmed CD4(+)T Cells: Differentiation and Functions
title_short CD4(+)T Cells: Differentiation and Functions
title_sort cd4(+)t cells: differentiation and functions
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312336/
https://www.ncbi.nlm.nih.gov/pubmed/22474485
http://dx.doi.org/10.1155/2012/925135
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