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...
- 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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|
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 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.coar.none.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.coarversion.none.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.driver.none.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.version.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
http://purl.org/coar/resource_type/c_6501 |
status_str |
publishedVersion |
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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1814246866389303296 |
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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