A TGF-? mediated regulatory mechanism modulates the T cell immune response to rotavirus in adults but not in children

Children with acute RV-gastroenteritis (GE) had low or undetectable levels of circulating IFN-?+, IL-13+, IL-2+, IL-10+ or IL-17+ RV-T cells. IFN-?+ T cells and low frequencies of IL-10+ and IL-2+ CD4+ T cells were found in adults with RV-GE during acute and convalescence phases, respectively. Circu...

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Tipo de recurso:
Fecha de publicación:
2010
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/27853
Acceso en línea:
https://doi.org/10.1016/j.virol.2009.12.016
https://repository.urosario.edu.co/handle/10336/27853
Palabra clave:
Rotavirus
Humans
Interferon-gamma
Interleukin 13
Interleukin-2
Interleukin-10
Interleukin-17
Transforming growth factor betaT-lymphocytes
T-lymphocytes
regulatory
Rights
License
Abierto (Texto Completo)
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spelling 288ba1b7-c490-4f52-852a-bba1aff3e44a-17b00af25-c0ab-48f7-bc3c-c32912c76197-123f75926-9ec4-4c06-8c16-aabefe1bb509-1ad2b2f75-6453-4b78-a59f-1db1a780a7db-1528960576002020-08-19T14:44:15Z2020-08-19T14:44:15Z2010-03-30Children with acute RV-gastroenteritis (GE) had low or undetectable levels of circulating IFN-?+, IL-13+, IL-2+, IL-10+ or IL-17+ RV-T cells. IFN-?+ T cells and low frequencies of IL-10+ and IL-2+ CD4+ T cells were found in adults with RV-GE during acute and convalescence phases, respectively. Circulating single IFN-?+ > double IFN-?+/IL-2+ > single IL-2+RV-CD4+T cells were observed in healthy adults. In this group, frequencies of IFN-?+ RV-T cells increased after removing CD25+cells, blocking TGF-? with its natural inhibitor, LAP, or inhibiting TGF-?RI signalling pathway with ALK5i. The frequencies of IFN-?+ RV-T cells were also incremented in PBMC depleted of CD25+cells and treated with ALK5i, suggesting that TGF? inhibition may be independent of Treg cells. The ALK5i effect was observed in adults but not in children with RV-GE, who had normal numbers of TGF-?+ Treg cells. Thus, a TGF-?-mediated regulatory mechanism that modulates RV-T cells in adults is not evident in children.application/pdfhttps://doi.org/10.1016/j.virol.2009.12.016ISSN: 0042-6822EISSN: 1096-0341https://repository.urosario.edu.co/handle/10336/27853engElsevier86No. 177VirologyVol. 399Virology, ISSN: 0042-6822;EISSN: 1096-0341, Vol.399, No.1 (2010); pp. 77-86https://www.sciencedirect.com/science/article/pii/S0042682209008010Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Virologyinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURRotavirusHumansInterferon-gammaInterleukin 13Interleukin-2Interleukin-10Interleukin-17Transforming growth factor betaT-lymphocytesT-lymphocytesregulatoryA TGF-? mediated regulatory mechanism modulates the T cell immune response to rotavirus in adults but not in childrenUn mecanismo regulador mediado por TGF-? modula la respuesta inmune de las células T al rotavirus en adultos pero no en niñosarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Mesa, Martha C.Gutiérrez, LinaAngel, JuanaFranco, Manuel A.Duarte-Rey, CarolinaORIGINALA_TGF__mediated_regulatory_mechanism_mo.pdfapplication/pdf872447https://repository.urosario.edu.co/bitstreams/66900d25-4435-4a8c-8dc4-9c0794223e25/download3926ad317a77a744fdb9c9237cedcb20MD51TEXTA_TGF__mediated_regulatory_mechanism_mo.pdf.txtA_TGF__mediated_regulatory_mechanism_mo.pdf.txtExtracted texttext/plain55981https://repository.urosario.edu.co/bitstreams/cbea4d5b-9e36-4f2b-82f0-1240a407ec2e/download4ad45a41d0b239598427a42608d0566eMD52THUMBNAILA_TGF__mediated_regulatory_mechanism_mo.pdf.jpgA_TGF__mediated_regulatory_mechanism_mo.pdf.jpgGenerated Thumbnailimage/jpeg4431https://repository.urosario.edu.co/bitstreams/d131f3f0-29d4-4d8d-9f62-acc1bbea820e/downloadb28b941de4410e596ef09d6969a6fdffMD5310336/27853oai:repository.urosario.edu.co:10336/278532021-06-03 00:51:04.868https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv A TGF-? mediated regulatory mechanism modulates the T cell immune response to rotavirus in adults but not in children
dc.title.TranslatedTitle.spa.fl_str_mv Un mecanismo regulador mediado por TGF-? modula la respuesta inmune de las células T al rotavirus en adultos pero no en niños
title A TGF-? mediated regulatory mechanism modulates the T cell immune response to rotavirus in adults but not in children
spellingShingle A TGF-? mediated regulatory mechanism modulates the T cell immune response to rotavirus in adults but not in children
Rotavirus
Humans
Interferon-gamma
Interleukin 13
Interleukin-2
Interleukin-10
Interleukin-17
Transforming growth factor betaT-lymphocytes
T-lymphocytes
regulatory
title_short A TGF-? mediated regulatory mechanism modulates the T cell immune response to rotavirus in adults but not in children
title_full A TGF-? mediated regulatory mechanism modulates the T cell immune response to rotavirus in adults but not in children
title_fullStr A TGF-? mediated regulatory mechanism modulates the T cell immune response to rotavirus in adults but not in children
title_full_unstemmed A TGF-? mediated regulatory mechanism modulates the T cell immune response to rotavirus in adults but not in children
title_sort A TGF-? mediated regulatory mechanism modulates the T cell immune response to rotavirus in adults but not in children
dc.subject.keyword.spa.fl_str_mv Rotavirus
Humans
Interferon-gamma
Interleukin 13
Interleukin-2
Interleukin-10
Interleukin-17
Transforming growth factor betaT-lymphocytes
T-lymphocytes
regulatory
topic Rotavirus
Humans
Interferon-gamma
Interleukin 13
Interleukin-2
Interleukin-10
Interleukin-17
Transforming growth factor betaT-lymphocytes
T-lymphocytes
regulatory
description Children with acute RV-gastroenteritis (GE) had low or undetectable levels of circulating IFN-?+, IL-13+, IL-2+, IL-10+ or IL-17+ RV-T cells. IFN-?+ T cells and low frequencies of IL-10+ and IL-2+ CD4+ T cells were found in adults with RV-GE during acute and convalescence phases, respectively. Circulating single IFN-?+ > double IFN-?+/IL-2+ > single IL-2+RV-CD4+T cells were observed in healthy adults. In this group, frequencies of IFN-?+ RV-T cells increased after removing CD25+cells, blocking TGF-? with its natural inhibitor, LAP, or inhibiting TGF-?RI signalling pathway with ALK5i. The frequencies of IFN-?+ RV-T cells were also incremented in PBMC depleted of CD25+cells and treated with ALK5i, suggesting that TGF? inhibition may be independent of Treg cells. The ALK5i effect was observed in adults but not in children with RV-GE, who had normal numbers of TGF-?+ Treg cells. Thus, a TGF-?-mediated regulatory mechanism that modulates RV-T cells in adults is not evident in children.
publishDate 2010
dc.date.created.spa.fl_str_mv 2010-03-30
dc.date.accessioned.none.fl_str_mv 2020-08-19T14:44:15Z
dc.date.available.none.fl_str_mv 2020-08-19T14:44:15Z
dc.type.eng.fl_str_mv article
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dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.virol.2009.12.016
dc.identifier.issn.none.fl_str_mv ISSN: 0042-6822
EISSN: 1096-0341
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/27853
url https://doi.org/10.1016/j.virol.2009.12.016
https://repository.urosario.edu.co/handle/10336/27853
identifier_str_mv ISSN: 0042-6822
EISSN: 1096-0341
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 86
dc.relation.citationIssue.none.fl_str_mv No. 1
dc.relation.citationStartPage.none.fl_str_mv 77
dc.relation.citationTitle.none.fl_str_mv Virology
dc.relation.citationVolume.none.fl_str_mv Vol. 399
dc.relation.ispartof.spa.fl_str_mv Virology, ISSN: 0042-6822;EISSN: 1096-0341, Vol.399, No.1 (2010); pp. 77-86
dc.relation.uri.spa.fl_str_mv https://www.sciencedirect.com/science/article/pii/S0042682209008010
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rights_invalid_str_mv Abierto (Texto Completo)
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dc.publisher.spa.fl_str_mv Elsevier
dc.source.spa.fl_str_mv Virology
institution Universidad del Rosario
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dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
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