HIV Type 1 Infection Up-Regulates TLR2 and TLR4 Expression and Function in Vivo and in Vitro

ABSTRACT: Toll-like receptors (TLRs) play a critical role in innate immunity against pathogens. Their stimulation induces the activation of NF-κB, an important inducer of HIV-1 replication. In recent years, an increasing number of studies using several cells types from HIV-infected patients indicate...

Full description

Autores:
Hernández López, Juan Carlos
Urcuqui Inchima, Silvio
Stevenson, Mario
Latz, Eicke
Tipo de recurso:
Article of investigation
Fecha de publicación:
2012
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/42185
Acceso en línea:
https://hdl.handle.net/10495/42185
Palabra clave:
Síndrome de Inmunodeficiencia Adquirida
Acquired Immunodeficiency Syndrome
Células dendríticas
Dendritic Cells
Regulación viral de la expresión génetica
Gene Expression Regulation, Viral
Inmunidad innata
Immunity, Innate
ARN
RNA
Carga viral
Viral Load
VIH-1
HIV-1
Macrófagos
Macrophages
Recuento de linfocitos CD4
CD4 Lymphocyte Count
Citometría de flujo
Flow Cytometry
https://id.nlm.nih.gov/mesh/D000163
https://id.nlm.nih.gov/mesh/D018791
https://id.nlm.nih.gov/mesh/D003713
https://id.nlm.nih.gov/mesh/D005434
https://id.nlm.nih.gov/mesh/D015967
https://id.nlm.nih.gov/mesh/D007113
https://id.nlm.nih.gov/mesh/D008264
https://id.nlm.nih.gov/mesh/D012313
https://id.nlm.nih.gov/mesh/D019562
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc/2.5/co/
id UDEA2_a9e56ab03c6e1a80851e955535db41a1
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/42185
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv HIV Type 1 Infection Up-Regulates TLR2 and TLR4 Expression and Function in Vivo and in Vitro
title HIV Type 1 Infection Up-Regulates TLR2 and TLR4 Expression and Function in Vivo and in Vitro
spellingShingle HIV Type 1 Infection Up-Regulates TLR2 and TLR4 Expression and Function in Vivo and in Vitro
Síndrome de Inmunodeficiencia Adquirida
Acquired Immunodeficiency Syndrome
Células dendríticas
Dendritic Cells
Regulación viral de la expresión génetica
Gene Expression Regulation, Viral
Inmunidad innata
Immunity, Innate
ARN
RNA
Carga viral
Viral Load
VIH-1
HIV-1
Macrófagos
Macrophages
Recuento de linfocitos CD4
CD4 Lymphocyte Count
Citometría de flujo
Flow Cytometry
https://id.nlm.nih.gov/mesh/D000163
https://id.nlm.nih.gov/mesh/D018791
https://id.nlm.nih.gov/mesh/D003713
https://id.nlm.nih.gov/mesh/D005434
https://id.nlm.nih.gov/mesh/D015967
https://id.nlm.nih.gov/mesh/D007113
https://id.nlm.nih.gov/mesh/D008264
https://id.nlm.nih.gov/mesh/D012313
https://id.nlm.nih.gov/mesh/D019562
title_short HIV Type 1 Infection Up-Regulates TLR2 and TLR4 Expression and Function in Vivo and in Vitro
title_full HIV Type 1 Infection Up-Regulates TLR2 and TLR4 Expression and Function in Vivo and in Vitro
title_fullStr HIV Type 1 Infection Up-Regulates TLR2 and TLR4 Expression and Function in Vivo and in Vitro
title_full_unstemmed HIV Type 1 Infection Up-Regulates TLR2 and TLR4 Expression and Function in Vivo and in Vitro
title_sort HIV Type 1 Infection Up-Regulates TLR2 and TLR4 Expression and Function in Vivo and in Vitro
dc.creator.fl_str_mv Hernández López, Juan Carlos
Urcuqui Inchima, Silvio
Stevenson, Mario
Latz, Eicke
dc.contributor.author.none.fl_str_mv Hernández López, Juan Carlos
Urcuqui Inchima, Silvio
Stevenson, Mario
Latz, Eicke
dc.contributor.researchgroup.spa.fl_str_mv Inmunovirología
dc.subject.decs.none.fl_str_mv Síndrome de Inmunodeficiencia Adquirida
Acquired Immunodeficiency Syndrome
Células dendríticas
Dendritic Cells
Regulación viral de la expresión génetica
Gene Expression Regulation, Viral
Inmunidad innata
Immunity, Innate
ARN
RNA
Carga viral
Viral Load
VIH-1
HIV-1
Macrófagos
Macrophages
Recuento de linfocitos CD4
CD4 Lymphocyte Count
Citometría de flujo
Flow Cytometry
topic Síndrome de Inmunodeficiencia Adquirida
Acquired Immunodeficiency Syndrome
Células dendríticas
Dendritic Cells
Regulación viral de la expresión génetica
Gene Expression Regulation, Viral
Inmunidad innata
Immunity, Innate
ARN
RNA
Carga viral
Viral Load
VIH-1
HIV-1
Macrófagos
Macrophages
Recuento de linfocitos CD4
CD4 Lymphocyte Count
Citometría de flujo
Flow Cytometry
https://id.nlm.nih.gov/mesh/D000163
https://id.nlm.nih.gov/mesh/D018791
https://id.nlm.nih.gov/mesh/D003713
https://id.nlm.nih.gov/mesh/D005434
https://id.nlm.nih.gov/mesh/D015967
https://id.nlm.nih.gov/mesh/D007113
https://id.nlm.nih.gov/mesh/D008264
https://id.nlm.nih.gov/mesh/D012313
https://id.nlm.nih.gov/mesh/D019562
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D000163
https://id.nlm.nih.gov/mesh/D018791
https://id.nlm.nih.gov/mesh/D003713
https://id.nlm.nih.gov/mesh/D005434
https://id.nlm.nih.gov/mesh/D015967
https://id.nlm.nih.gov/mesh/D007113
https://id.nlm.nih.gov/mesh/D008264
https://id.nlm.nih.gov/mesh/D012313
https://id.nlm.nih.gov/mesh/D019562
description ABSTRACT: Toll-like receptors (TLRs) play a critical role in innate immunity against pathogens. Their stimulation induces the activation of NF-κB, an important inducer of HIV-1 replication. In recent years, an increasing number of studies using several cells types from HIV-infected patients indicate that TLRs play a key role in regulating the expression of proinflammatory cytokines and viral pathogenesis. In the present study, the effect of HIV-1 stimulation of monocyte-derived macrophage (MDM) and peripheral blood mononuclear cell (PBMC) subpopulations from healthy donors on the expression and functions of TLR2 and TLR4 was examined. In addition, and to complete the in vitro study, the expression pattern of TLR2 and TLR4 in 49 HIV-1-infected patients, classified according to viral load and the use of HAART, was determined and compared with 25 healthy subjects. An increase of TLR expression and production of proinflammatory cytokines were observed in MDMs and PBMCs infected with HIV-1 in vitro and in response to TLR stimulation, compared to the mock. In addition, an association between TLR expression and up-regulation of CD80 in plasmacytoid dendritic cells (pDCs) was observed. The ex vivo analysis indicated increased expression of TLR2 and TLR4 in myeloid dendritic cells (mDCs), but only of TLR2 in monocytes obtained from HIV-1-infected patients, compared to healthy subjects. Remarkably, the expression was higher in cells from patients who do not use HAART. In monocytes, there was a positive correlation between both TLRs and viral load, but not CD4(+) T cell numbers. Together, our in vitro and ex vivo results suggest that TLR expression and function can be up-regulated in response to HIV-1 infection and could affect the inflammatory response. We propose that modulation of TLRs represents a mechanism to promote HIV-1 replication or AIDS progression in HIV-1-infected patients.
publishDate 2012
dc.date.issued.none.fl_str_mv 2012
dc.date.accessioned.none.fl_str_mv 2024-09-16T21:41:31Z
dc.date.available.none.fl_str_mv 2024-09-16T21:41:31Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
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dc.identifier.citation.spa.fl_str_mv Hernández JC, Stevenson M, Latz E, Urcuqui-Inchima S. HIV type 1 infection up-regulates TLR2 and TLR4 expression and function in vivo and in vitro. AIDS Res Hum Retroviruses. 2012 Oct;28(10):1313-28. doi: 10.1089/aid.2011.0297.
dc.identifier.issn.none.fl_str_mv 0889-2229
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/42185
dc.identifier.doi.none.fl_str_mv 10.1089/aid.2011.0297
dc.identifier.eissn.none.fl_str_mv 1931-8405
identifier_str_mv Hernández JC, Stevenson M, Latz E, Urcuqui-Inchima S. HIV type 1 infection up-regulates TLR2 and TLR4 expression and function in vivo and in vitro. AIDS Res Hum Retroviruses. 2012 Oct;28(10):1313-28. doi: 10.1089/aid.2011.0297.
0889-2229
10.1089/aid.2011.0297
1931-8405
url https://hdl.handle.net/10495/42185
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv AIDS Res. Hum. Retroviruses.
dc.relation.citationendpage.spa.fl_str_mv 1328
dc.relation.citationissue.spa.fl_str_mv 10
dc.relation.citationstartpage.spa.fl_str_mv 1313
dc.relation.citationvolume.spa.fl_str_mv 28
dc.relation.ispartofjournal.spa.fl_str_mv AIDS Research and Human Retroviruses
dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by-nc/2.5/co/
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dc.format.extent.spa.fl_str_mv 16 páginas
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Mary Ann Liebert
dc.publisher.place.spa.fl_str_mv Nueva York, Estados Unidos
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spelling Hernández López, Juan CarlosUrcuqui Inchima, SilvioStevenson, MarioLatz, EickeInmunovirología2024-09-16T21:41:31Z2024-09-16T21:41:31Z2012Hernández JC, Stevenson M, Latz E, Urcuqui-Inchima S. HIV type 1 infection up-regulates TLR2 and TLR4 expression and function in vivo and in vitro. AIDS Res Hum Retroviruses. 2012 Oct;28(10):1313-28. doi: 10.1089/aid.2011.0297.0889-2229https://hdl.handle.net/10495/4218510.1089/aid.2011.02971931-8405ABSTRACT: Toll-like receptors (TLRs) play a critical role in innate immunity against pathogens. Their stimulation induces the activation of NF-κB, an important inducer of HIV-1 replication. In recent years, an increasing number of studies using several cells types from HIV-infected patients indicate that TLRs play a key role in regulating the expression of proinflammatory cytokines and viral pathogenesis. In the present study, the effect of HIV-1 stimulation of monocyte-derived macrophage (MDM) and peripheral blood mononuclear cell (PBMC) subpopulations from healthy donors on the expression and functions of TLR2 and TLR4 was examined. In addition, and to complete the in vitro study, the expression pattern of TLR2 and TLR4 in 49 HIV-1-infected patients, classified according to viral load and the use of HAART, was determined and compared with 25 healthy subjects. An increase of TLR expression and production of proinflammatory cytokines were observed in MDMs and PBMCs infected with HIV-1 in vitro and in response to TLR stimulation, compared to the mock. In addition, an association between TLR expression and up-regulation of CD80 in plasmacytoid dendritic cells (pDCs) was observed. The ex vivo analysis indicated increased expression of TLR2 and TLR4 in myeloid dendritic cells (mDCs), but only of TLR2 in monocytes obtained from HIV-1-infected patients, compared to healthy subjects. Remarkably, the expression was higher in cells from patients who do not use HAART. In monocytes, there was a positive correlation between both TLRs and viral load, but not CD4(+) T cell numbers. Together, our in vitro and ex vivo results suggest that TLR expression and function can be up-regulated in response to HIV-1 infection and could affect the inflammatory response. We propose that modulation of TLRs represents a mechanism to promote HIV-1 replication or AIDS progression in HIV-1-infected patients.Colombia. Ministerio de Ciencia, Tecnología e Innovación - MinCienciasNational Institutes of HealthCOL001244416 páginasapplication/pdfengMary Ann LiebertNueva York, Estados Unidoshttp://creativecommons.org/licenses/by-nc/2.5/co/https://creativecommons.org/licenses/by-nc/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2HIV Type 1 Infection Up-Regulates TLR2 and TLR4 Expression and Function in Vivo and in VitroArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionSíndrome de Inmunodeficiencia AdquiridaAcquired Immunodeficiency SyndromeCélulas dendríticasDendritic CellsRegulación viral de la expresión géneticaGene Expression Regulation, ViralInmunidad innataImmunity, InnateARNRNACarga viralViral LoadVIH-1HIV-1MacrófagosMacrophagesRecuento de linfocitos CD4CD4 Lymphocyte CountCitometría de flujoFlow Cytometryhttps://id.nlm.nih.gov/mesh/D000163https://id.nlm.nih.gov/mesh/D018791https://id.nlm.nih.gov/mesh/D003713https://id.nlm.nih.gov/mesh/D005434https://id.nlm.nih.gov/mesh/D015967https://id.nlm.nih.gov/mesh/D007113https://id.nlm.nih.gov/mesh/D008264https://id.nlm.nih.gov/mesh/D012313https://id.nlm.nih.gov/mesh/D019562AIDS Res. 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