Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS

The spontaneous control of HIV replication in HIV-controllers underlines the importance of these subjects for exploring factors related to delayed progression. Several studies have revealed fewer immune alterations and effector mechanisms related to viral control, mainly in peripheral blood, in thes...

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Autores:
González, Sandra Milena
Taborda, Natalia Andrea
Correa, Luis A.
Castro, Gustavo A.
Hernández López, Juan Carlos
Montoya, Carlos Julio
Rugeles López, María Teresa
Tipo de recurso:
Article of journal
Fecha de publicación:
2016
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
Idioma:
OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/1178
Acceso en línea:
https://hdl.handle.net/20.500.12494/1178
Palabra clave:
Immune regulation
HIV-1 controllers
Rights
embargoedAccess
License
Licencia CC
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network_name_str Repositorio UCC
repository_id_str
dc.title.spa.fl_str_mv Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS
title Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS
spellingShingle Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS
Immune regulation
HIV-1 controllers
title_short Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS
title_full Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS
title_fullStr Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS
title_full_unstemmed Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS
title_sort Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS
dc.creator.fl_str_mv González, Sandra Milena
Taborda, Natalia Andrea
Correa, Luis A.
Castro, Gustavo A.
Hernández López, Juan Carlos
Montoya, Carlos Julio
Rugeles López, María Teresa
dc.contributor.author.none.fl_str_mv González, Sandra Milena
Taborda, Natalia Andrea
Correa, Luis A.
Castro, Gustavo A.
Hernández López, Juan Carlos
Montoya, Carlos Julio
Rugeles López, María Teresa
dc.subject.spa.fl_str_mv Immune regulation
HIV-1 controllers
topic Immune regulation
HIV-1 controllers
description The spontaneous control of HIV replication in HIV-controllers underlines the importance of these subjects for exploring factors related to delayed progression. Several studies have revealed fewer immune alterations and effector mechanisms related to viral control, mainly in peripheral blood, in these individuals compared to normal progressors. However, immune characterization of gut-associated lymphoid tissue (GALT), the major target of infection, has not been thoroughly explored in these subjects. We evaluated the following parameters in GALT samples from 11 HIV-controllers and 15 HIV-progressors: (i) frequency and activation phenotype of T cells; (ii) expression of transcription factors associated with immune response profiles; and (iii) frequency of apoptotic cells. Interestingly, HIV-controllers exhibited a particular activation phenotype, with predominance of T cells expressing HLA-DR but not CD38 in GALT. This phenotype, previously associated with better control of infection, was correlated with low viral load and higher CD4? T cell count. Furthermore, a positive correlation of this activation phenotype with higher expression of Foxp3 and RORcT transcription factors suggested a key role for Treg and Th17 cells in the control of the immune activation and in the maintenance of gut mucosal integrity. Although we evaluated apoptosis by measuring expression of cleaved caspase-3 in GALT, we did not find differences between HIV-controllers and HIV-progressors. Taken together, our findings suggest that predominance of HLA-DR+ T cells, along with lower immune activation and higher expression of transcription factors required for the development of Treg and Th17 cells, is associated with better viral control and delayed progression to AIDS.
publishDate 2016
dc.date.issued.none.fl_str_mv 2016-01
dc.date.accessioned.none.fl_str_mv 2017-08-18T20:41:37Z
dc.date.available.none.fl_str_mv 2017-01
2017-08-18T20:41:37Z
dc.type.none.fl_str_mv Artículo
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dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12494/1178
dc.identifier.bibliographicCitation.spa.fl_str_mv González S.M., Taborda, N. A., Correa, L. A.; Castro, G. A, Hernández J. C., Montoya, C. J. & Rugeles, M. T. (2016). Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS. Immunologic Research, 64(3), 765-774. doi: 10.1007/s12026-015-8775-5
url https://hdl.handle.net/20.500.12494/1178
identifier_str_mv González S.M., Taborda, N. A., Correa, L. A.; Castro, G. A, Hernández J. C., Montoya, C. J. & Rugeles, M. T. (2016). Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS. Immunologic Research, 64(3), 765-774. doi: 10.1007/s12026-015-8775-5
dc.relation.isversionof.spa.fl_str_mv https://link.springer.com/article/10.1007%2Fs12026-015-8775-5
dc.rights.cc.none.fl_str_mv Licencia CC
dc.rights.accessrights.none.fl_str_mv info:eu-repo/semantics/embargoedAccess
dc.rights.coar.none.fl_str_mv http://purl.org/coar/access_right/c_f1cf
rights_invalid_str_mv Licencia CC
http://purl.org/coar/access_right/c_f1cf
eu_rights_str_mv embargoedAccess
dc.publisher.spa.fl_str_mv Universidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Programa de Medicina, Medellín y Envigado, Colombia, 00000
dc.publisher.program.spa.fl_str_mv Medicina
dc.publisher.place.spa.fl_str_mv Medellín
institution Universidad Cooperativa de Colombia
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spelling González, Sandra MilenaTaborda, Natalia AndreaCorrea, Luis A.Castro, Gustavo A.Hernández López, Juan CarlosMontoya, Carlos JulioRugeles López, María Teresa2017-08-18T20:41:37Z2017-012017-08-18T20:41:37Z2016-01https://hdl.handle.net/20.500.12494/1178González S.M., Taborda, N. A., Correa, L. A.; Castro, G. A, Hernández J. C., Montoya, C. J. & Rugeles, M. T. (2016). Particular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDS. Immunologic Research, 64(3), 765-774. doi: 10.1007/s12026-015-8775-5The spontaneous control of HIV replication in HIV-controllers underlines the importance of these subjects for exploring factors related to delayed progression. Several studies have revealed fewer immune alterations and effector mechanisms related to viral control, mainly in peripheral blood, in these individuals compared to normal progressors. However, immune characterization of gut-associated lymphoid tissue (GALT), the major target of infection, has not been thoroughly explored in these subjects. We evaluated the following parameters in GALT samples from 11 HIV-controllers and 15 HIV-progressors: (i) frequency and activation phenotype of T cells; (ii) expression of transcription factors associated with immune response profiles; and (iii) frequency of apoptotic cells. Interestingly, HIV-controllers exhibited a particular activation phenotype, with predominance of T cells expressing HLA-DR but not CD38 in GALT. This phenotype, previously associated with better control of infection, was correlated with low viral load and higher CD4? T cell count. Furthermore, a positive correlation of this activation phenotype with higher expression of Foxp3 and RORcT transcription factors suggested a key role for Treg and Th17 cells in the control of the immune activation and in the maintenance of gut mucosal integrity. Although we evaluated apoptosis by measuring expression of cleaved caspase-3 in GALT, we did not find differences between HIV-controllers and HIV-progressors. Taken together, our findings suggest that predominance of HLA-DR+ T cells, along with lower immune activation and higher expression of transcription factors required for the development of Treg and Th17 cells, is associated with better viral control and delayed progression to AIDS.juanc.hernandezl@campusucc.edu.coUniversidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Programa de Medicina, Medellín y Envigado, Colombia, 00000MedicinaMedellínhttps://link.springer.com/article/10.1007%2Fs12026-015-8775-5Immune regulationHIV-1 controllersParticular activation phenotype of T cells expressing HLA-DR but not CD38 in GALT from HIV-controllers is associated with immune regulation and delayed progression to AIDSArtículohttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1http://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionLicencia 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