HIV-1-Infected children on HAART: Immunologic features of three different levels of viral suppression

Detalhes bibliográficos
Autor(a) principal: Zaccarelli Filho, Carlos Alberto [UNIFESP]
Data de Publicação: 2007
Outros Autores: Ono, Erika [UNIFESP], Machado, Daisy Maria [UNIFESP], Brunialti, Milena Karina Coló [UNIFESP], Succi, Regina Célia de Menezes [UNIFESP], Salomão, Reinaldo [UNIFESP], Kallas, Esper Georges [UNIFESP], De Moraes-Pinto, Maria Isabel [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/29456
http://dx.doi.org/10.1002/cyto.b.20152
Resumo: Background: HIV-1-infected children show changes of blood lymphocyte subpopulations. We have, therefore, investigated how highly active anti-retroviral therapy (ART) alter these subsets. Blood samples were taken from 41 HIV-1-infected children on ART who were divided into groups showing good, partial and poor responses to ART on the basis of viral load (VL) measurement in blood. the observations were compared to those seen in 20 uninfected children.Methods: the samples were studied using 4-color flow cytometry for naive, central memory and effector memory cells as well as for CD38 expression as the sign of activation within both the CD4+ and the CD8+ T cell populations. HIV-1 infected children were also evaluated for the presence and the titers of antibodies induced by vaccination against childhood infections in our patients while on HAART.Results: Lymphocyte counts were lower in the poor viral load responding (VLR) group when compared with partial and good VLRs. Poor VLRs had lower total and naive CD4+ T cell counts. HIV-1-infected children from all three groups had high CD8+ T cell counts. Central memory CD4+ and CD8+ T cell percentages were particularly low in the poor VLR group while in the poor VLR group the percentages of effector memory CD4+ and CD8+ T cells were higher when compared with the control group. Higher cellular activation of CD8+ T cells was observed in HIV-1-infected children, particularly when analyzed for the intensity of CD38 expression in the poor VLR group. CD5 expression on B cells was higher among all HIV-1-infected children. Antibodies to tetanus, diphtheria, measles, rubella, and hepatitis B were present in a large proportion of children but the titers were similarly low for all three groups of HIV-infected children.Conclusions: Children with different levels of viral response to HAART present immune phenotype characteristics that tend to place the children with partial and good virological responses into the same group. These children are still moderately deficient in their immune responses but show better recovery than seen with children in the poor VLR group. These observations indicate that the proportions of central memory cells among the CD4+ T cells and the intensity of the expression of CD38 activation antigen on CD8+ T cells provide more informative parameters for monitoring children on HAART than the absolute numbers of CD4+ and CD8+ T cells alone. (c) 2006 Clinical Cytometry Society.
id UFSP_d5f005b2b93d23821c66e0e05608fb42
oai_identifier_str oai:repositorio.unifesp.br:11600/29456
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Zaccarelli Filho, Carlos Alberto [UNIFESP]Ono, Erika [UNIFESP]Machado, Daisy Maria [UNIFESP]Brunialti, Milena Karina Coló [UNIFESP]Succi, Regina Célia de Menezes [UNIFESP]Salomão, Reinaldo [UNIFESP]Kallas, Esper Georges [UNIFESP]De Moraes-Pinto, Maria Isabel [UNIFESP]Universidade Federal de São Paulo (UNIFESP)2016-01-24T12:41:49Z2016-01-24T12:41:49Z2007-01-15Cytometry Part B-clinical Cytometry. Hoboken: Wiley-liss, v. 72B, n. 1, p. 14-21, 2007.1552-4949http://repositorio.unifesp.br/handle/11600/29456http://dx.doi.org/10.1002/cyto.b.2015210.1002/cyto.b.20152WOS:000243322000004Background: HIV-1-infected children show changes of blood lymphocyte subpopulations. We have, therefore, investigated how highly active anti-retroviral therapy (ART) alter these subsets. Blood samples were taken from 41 HIV-1-infected children on ART who were divided into groups showing good, partial and poor responses to ART on the basis of viral load (VL) measurement in blood. the observations were compared to those seen in 20 uninfected children.Methods: the samples were studied using 4-color flow cytometry for naive, central memory and effector memory cells as well as for CD38 expression as the sign of activation within both the CD4+ and the CD8+ T cell populations. HIV-1 infected children were also evaluated for the presence and the titers of antibodies induced by vaccination against childhood infections in our patients while on HAART.Results: Lymphocyte counts were lower in the poor viral load responding (VLR) group when compared with partial and good VLRs. Poor VLRs had lower total and naive CD4+ T cell counts. HIV-1-infected children from all three groups had high CD8+ T cell counts. Central memory CD4+ and CD8+ T cell percentages were particularly low in the poor VLR group while in the poor VLR group the percentages of effector memory CD4+ and CD8+ T cells were higher when compared with the control group. Higher cellular activation of CD8+ T cells was observed in HIV-1-infected children, particularly when analyzed for the intensity of CD38 expression in the poor VLR group. CD5 expression on B cells was higher among all HIV-1-infected children. Antibodies to tetanus, diphtheria, measles, rubella, and hepatitis B were present in a large proportion of children but the titers were similarly low for all three groups of HIV-infected children.Conclusions: Children with different levels of viral response to HAART present immune phenotype characteristics that tend to place the children with partial and good virological responses into the same group. These children are still moderately deficient in their immune responses but show better recovery than seen with children in the poor VLR group. These observations indicate that the proportions of central memory cells among the CD4+ T cells and the intensity of the expression of CD38 activation antigen on CD8+ T cells provide more informative parameters for monitoring children on HAART than the absolute numbers of CD4+ and CD8+ T cells alone. (c) 2006 Clinical Cytometry Society.Universidade Federal de São Paulo, Res Lab, Div Pediat Infect Dis, BR-04039032 São Paulo, SP, BrazilUniversidade Federal de São Paulo, Div Infect Dis, São Paulo, BrazilUniversidade Federal de São Paulo, Res Lab, Div Pediat Infect Dis, BR-04039032 São Paulo, SP, BrazilUniversidade Federal de São Paulo, Div Infect Dis, São Paulo, BrazilWeb of Science14-21engWiley-BlackwellCytometry Part B-clinical Cytometryhttp://olabout.wiley.com/WileyCDA/Section/id-406071.htmlinfo:eu-repo/semantics/openAccessHIV-infected childrenantiretroviral therapyimmune reconstitutionHIV-1-Infected children on HAART: Immunologic features of three different levels of viral suppressioninfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlereponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/294562022-09-27 09:48:38.485metadata only accessoai:repositorio.unifesp.br:11600/29456Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:23:46.350315Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv HIV-1-Infected children on HAART: Immunologic features of three different levels of viral suppression
title HIV-1-Infected children on HAART: Immunologic features of three different levels of viral suppression
spellingShingle HIV-1-Infected children on HAART: Immunologic features of three different levels of viral suppression
Zaccarelli Filho, Carlos Alberto [UNIFESP]
HIV-infected children
antiretroviral therapy
immune reconstitution
title_short HIV-1-Infected children on HAART: Immunologic features of three different levels of viral suppression
title_full HIV-1-Infected children on HAART: Immunologic features of three different levels of viral suppression
title_fullStr HIV-1-Infected children on HAART: Immunologic features of three different levels of viral suppression
title_full_unstemmed HIV-1-Infected children on HAART: Immunologic features of three different levels of viral suppression
title_sort HIV-1-Infected children on HAART: Immunologic features of three different levels of viral suppression
author Zaccarelli Filho, Carlos Alberto [UNIFESP]
author_facet Zaccarelli Filho, Carlos Alberto [UNIFESP]
Ono, Erika [UNIFESP]
Machado, Daisy Maria [UNIFESP]
Brunialti, Milena Karina Coló [UNIFESP]
Succi, Regina Célia de Menezes [UNIFESP]
Salomão, Reinaldo [UNIFESP]
Kallas, Esper Georges [UNIFESP]
De Moraes-Pinto, Maria Isabel [UNIFESP]
author_role author
author2 Ono, Erika [UNIFESP]
Machado, Daisy Maria [UNIFESP]
Brunialti, Milena Karina Coló [UNIFESP]
Succi, Regina Célia de Menezes [UNIFESP]
Salomão, Reinaldo [UNIFESP]
Kallas, Esper Georges [UNIFESP]
De Moraes-Pinto, Maria Isabel [UNIFESP]
author2_role author
author
author
author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Zaccarelli Filho, Carlos Alberto [UNIFESP]
Ono, Erika [UNIFESP]
Machado, Daisy Maria [UNIFESP]
Brunialti, Milena Karina Coló [UNIFESP]
Succi, Regina Célia de Menezes [UNIFESP]
Salomão, Reinaldo [UNIFESP]
Kallas, Esper Georges [UNIFESP]
De Moraes-Pinto, Maria Isabel [UNIFESP]
dc.subject.eng.fl_str_mv HIV-infected children
antiretroviral therapy
immune reconstitution
topic HIV-infected children
antiretroviral therapy
immune reconstitution
description Background: HIV-1-infected children show changes of blood lymphocyte subpopulations. We have, therefore, investigated how highly active anti-retroviral therapy (ART) alter these subsets. Blood samples were taken from 41 HIV-1-infected children on ART who were divided into groups showing good, partial and poor responses to ART on the basis of viral load (VL) measurement in blood. the observations were compared to those seen in 20 uninfected children.Methods: the samples were studied using 4-color flow cytometry for naive, central memory and effector memory cells as well as for CD38 expression as the sign of activation within both the CD4+ and the CD8+ T cell populations. HIV-1 infected children were also evaluated for the presence and the titers of antibodies induced by vaccination against childhood infections in our patients while on HAART.Results: Lymphocyte counts were lower in the poor viral load responding (VLR) group when compared with partial and good VLRs. Poor VLRs had lower total and naive CD4+ T cell counts. HIV-1-infected children from all three groups had high CD8+ T cell counts. Central memory CD4+ and CD8+ T cell percentages were particularly low in the poor VLR group while in the poor VLR group the percentages of effector memory CD4+ and CD8+ T cells were higher when compared with the control group. Higher cellular activation of CD8+ T cells was observed in HIV-1-infected children, particularly when analyzed for the intensity of CD38 expression in the poor VLR group. CD5 expression on B cells was higher among all HIV-1-infected children. Antibodies to tetanus, diphtheria, measles, rubella, and hepatitis B were present in a large proportion of children but the titers were similarly low for all three groups of HIV-infected children.Conclusions: Children with different levels of viral response to HAART present immune phenotype characteristics that tend to place the children with partial and good virological responses into the same group. These children are still moderately deficient in their immune responses but show better recovery than seen with children in the poor VLR group. These observations indicate that the proportions of central memory cells among the CD4+ T cells and the intensity of the expression of CD38 activation antigen on CD8+ T cells provide more informative parameters for monitoring children on HAART than the absolute numbers of CD4+ and CD8+ T cells alone. (c) 2006 Clinical Cytometry Society.
publishDate 2007
dc.date.issued.fl_str_mv 2007-01-15
dc.date.accessioned.fl_str_mv 2016-01-24T12:41:49Z
dc.date.available.fl_str_mv 2016-01-24T12:41:49Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Cytometry Part B-clinical Cytometry. Hoboken: Wiley-liss, v. 72B, n. 1, p. 14-21, 2007.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/29456
http://dx.doi.org/10.1002/cyto.b.20152
dc.identifier.issn.none.fl_str_mv 1552-4949
dc.identifier.doi.none.fl_str_mv 10.1002/cyto.b.20152
dc.identifier.wos.none.fl_str_mv WOS:000243322000004
identifier_str_mv Cytometry Part B-clinical Cytometry. Hoboken: Wiley-liss, v. 72B, n. 1, p. 14-21, 2007.
1552-4949
10.1002/cyto.b.20152
WOS:000243322000004
url http://repositorio.unifesp.br/handle/11600/29456
http://dx.doi.org/10.1002/cyto.b.20152
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Cytometry Part B-clinical Cytometry
dc.rights.driver.fl_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 14-21
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
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
_version_ 1783460285457104896