Follicular helper t cell in immunity and autoimmunity
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo (review) |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
dARK ID: | ark:/48912/00130000022fs |
Texto Completo: | http://dx.doi.org/10.1590/1414-431X20165209 http://repositorio.unifesp.br/handle/11600/49499 |
Resumo: | The traditional concept that effector T helper (Th) responses are mediated by Th1/Th2 cell subtypes has been broadened by the recent demonstration of two new effector T helper cells, the IL-17 producing cells (Th17) and the follicular helper T cells (Tfh). These new subsets have many features in common, such as the ability to produce IL-21 and to express the IL-23 receptor (IL23R), the inducible costimulatory molecule ICOS, and the transcription factor c-Maf, all of them essential for expansion and establishment of the final pool of both subsets. Tfh cells differ from Th17 by their ability to home to B cell areas in secondary lymphoid tissue through interactions mediated by the chemokine receptor CXCR5 and its ligand CXCL13. These CXCR5(+) CD4(+) T cells are considered an effector T cell type specialized in B cell help, with a transcriptional profile distinct from Th1 and Th2 cells. The role of Tfh cells and its primary product, IL-21, on B-cell activation and differentiation is essential for humoral immunity against infectious agents. However, when deregulated, Tfh cells could represent an important mechanism contributing to exacerbated humoral response and autoantibody production in autoimmune diseases. This review highlights the importance of Tfh cells by focusing on their biology and differentiation processes in the context of normal immune response to infectious microorganisms and their role in the pathogenesis of autoimmune diseases. |
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Follicular helper t cell in immunity and autoimmunityAutoimmune DiseasesTfhLymphoid TissueHumoral ImmunitySystemic-Lupus-ErythematosusB-CellMyasthenia-GravisRheumatoid-ArthritisInducible CostimulatorCutting EdgePlasma-CellsInterleukin-21 ReceptorSjogrens-SyndromeHumoral ImmunityThe traditional concept that effector T helper (Th) responses are mediated by Th1/Th2 cell subtypes has been broadened by the recent demonstration of two new effector T helper cells, the IL-17 producing cells (Th17) and the follicular helper T cells (Tfh). These new subsets have many features in common, such as the ability to produce IL-21 and to express the IL-23 receptor (IL23R), the inducible costimulatory molecule ICOS, and the transcription factor c-Maf, all of them essential for expansion and establishment of the final pool of both subsets. Tfh cells differ from Th17 by their ability to home to B cell areas in secondary lymphoid tissue through interactions mediated by the chemokine receptor CXCR5 and its ligand CXCL13. These CXCR5(+) CD4(+) T cells are considered an effector T cell type specialized in B cell help, with a transcriptional profile distinct from Th1 and Th2 cells. The role of Tfh cells and its primary product, IL-21, on B-cell activation and differentiation is essential for humoral immunity against infectious agents. However, when deregulated, Tfh cells could represent an important mechanism contributing to exacerbated humoral response and autoantibody production in autoimmune diseases. This review highlights the importance of Tfh cells by focusing on their biology and differentiation processes in the context of normal immune response to infectious microorganisms and their role in the pathogenesis of autoimmune diseases.Divisão de Reumatologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, BrasilDivisão de Farmacologia, Instituto de Ciências Biológicas, Universidade de São Paulo, São Paulo, SP, BrasilDivisão de Imunologia, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, BrasilEscola de Ciências Médicas, Farmacêuticas e Biomédicas, Pontifícia Universidade Católica de Goiás, Goiânia, GO, BrasilDivisão de Reumatologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, BrasilWeb of ScienceAssoc bras divulg cientifica2019-01-21T10:29:57Z2019-01-21T10:29:57Z2016info:eu-repo/semantics/reviewinfo:eu-repo/semantics/publishedVersione5209http://dx.doi.org/10.1590/1414-431X20165209Brazilian Journal Of Medical And Biological Research. Sao paulo, v. 49, n. 5, p. e5209, 2016.10.1590/1414-431X20165209S0100-879X2016000500302.pdf0100-879XS0100-879X2016000500302http://repositorio.unifesp.br/handle/11600/49499WOS:000376684000007ark:/48912/00130000022fsengBrazilian Journal Of Medical And Biological Researchinfo:eu-repo/semantics/openAccessMesquita, D., Jr. [UNIFESP]Cruvinel, W. M. [UNIFESP]Resende, L. S.Mesquita, F. V. [UNIFESP]Silva, N. P. [UNIFESP]Camara, N. O. S.Andrade, L. E. C. [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2021-10-04T21:26:14Zoai:repositorio.unifesp.br/:11600/49499Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T19:51:53.332737Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Follicular helper t cell in immunity and autoimmunity |
title |
Follicular helper t cell in immunity and autoimmunity |
spellingShingle |
Follicular helper t cell in immunity and autoimmunity Mesquita, D., Jr. [UNIFESP] Autoimmune Diseases Tfh Lymphoid Tissue Humoral ImmunitySystemic-Lupus-Erythematosus B-Cell Myasthenia-Gravis Rheumatoid-Arthritis Inducible Costimulator Cutting Edge Plasma-Cells Interleukin-21 Receptor Sjogrens-Syndrome Humoral Immunity |
title_short |
Follicular helper t cell in immunity and autoimmunity |
title_full |
Follicular helper t cell in immunity and autoimmunity |
title_fullStr |
Follicular helper t cell in immunity and autoimmunity |
title_full_unstemmed |
Follicular helper t cell in immunity and autoimmunity |
title_sort |
Follicular helper t cell in immunity and autoimmunity |
author |
Mesquita, D., Jr. [UNIFESP] |
author_facet |
Mesquita, D., Jr. [UNIFESP] Cruvinel, W. M. [UNIFESP] Resende, L. S. Mesquita, F. V. [UNIFESP] Silva, N. P. [UNIFESP] Camara, N. O. S. Andrade, L. E. C. [UNIFESP] |
author_role |
author |
author2 |
Cruvinel, W. M. [UNIFESP] Resende, L. S. Mesquita, F. V. [UNIFESP] Silva, N. P. [UNIFESP] Camara, N. O. S. Andrade, L. E. C. [UNIFESP] |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Mesquita, D., Jr. [UNIFESP] Cruvinel, W. M. [UNIFESP] Resende, L. S. Mesquita, F. V. [UNIFESP] Silva, N. P. [UNIFESP] Camara, N. O. S. Andrade, L. E. C. [UNIFESP] |
dc.subject.por.fl_str_mv |
Autoimmune Diseases Tfh Lymphoid Tissue Humoral ImmunitySystemic-Lupus-Erythematosus B-Cell Myasthenia-Gravis Rheumatoid-Arthritis Inducible Costimulator Cutting Edge Plasma-Cells Interleukin-21 Receptor Sjogrens-Syndrome Humoral Immunity |
topic |
Autoimmune Diseases Tfh Lymphoid Tissue Humoral ImmunitySystemic-Lupus-Erythematosus B-Cell Myasthenia-Gravis Rheumatoid-Arthritis Inducible Costimulator Cutting Edge Plasma-Cells Interleukin-21 Receptor Sjogrens-Syndrome Humoral Immunity |
description |
The traditional concept that effector T helper (Th) responses are mediated by Th1/Th2 cell subtypes has been broadened by the recent demonstration of two new effector T helper cells, the IL-17 producing cells (Th17) and the follicular helper T cells (Tfh). These new subsets have many features in common, such as the ability to produce IL-21 and to express the IL-23 receptor (IL23R), the inducible costimulatory molecule ICOS, and the transcription factor c-Maf, all of them essential for expansion and establishment of the final pool of both subsets. Tfh cells differ from Th17 by their ability to home to B cell areas in secondary lymphoid tissue through interactions mediated by the chemokine receptor CXCR5 and its ligand CXCL13. These CXCR5(+) CD4(+) T cells are considered an effector T cell type specialized in B cell help, with a transcriptional profile distinct from Th1 and Th2 cells. The role of Tfh cells and its primary product, IL-21, on B-cell activation and differentiation is essential for humoral immunity against infectious agents. However, when deregulated, Tfh cells could represent an important mechanism contributing to exacerbated humoral response and autoantibody production in autoimmune diseases. This review highlights the importance of Tfh cells by focusing on their biology and differentiation processes in the context of normal immune response to infectious microorganisms and their role in the pathogenesis of autoimmune diseases. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 2019-01-21T10:29:57Z 2019-01-21T10:29:57Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/review |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
review |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/1414-431X20165209 Brazilian Journal Of Medical And Biological Research. Sao paulo, v. 49, n. 5, p. e5209, 2016. 10.1590/1414-431X20165209 S0100-879X2016000500302.pdf 0100-879X S0100-879X2016000500302 http://repositorio.unifesp.br/handle/11600/49499 WOS:000376684000007 |
dc.identifier.dark.fl_str_mv |
ark:/48912/00130000022fs |
url |
http://dx.doi.org/10.1590/1414-431X20165209 http://repositorio.unifesp.br/handle/11600/49499 |
identifier_str_mv |
Brazilian Journal Of Medical And Biological Research. Sao paulo, v. 49, n. 5, p. e5209, 2016. 10.1590/1414-431X20165209 S0100-879X2016000500302.pdf 0100-879X S0100-879X2016000500302 WOS:000376684000007 ark:/48912/00130000022fs |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Brazilian Journal Of Medical And Biological Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
e5209 |
dc.publisher.none.fl_str_mv |
Assoc bras divulg cientifica |
publisher.none.fl_str_mv |
Assoc bras divulg cientifica |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1818602385958764544 |