Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients

Detalhes bibliográficos
Autor(a) principal: Carvalho, Karina I.
Data de Publicação: 2012
Outros Autores: Bruno, Fernanda R., Snyder-Cappione, Jennifer E., Maeda, Solange M. [UNIFESP], Tomimori, Jane [UNIFESP], Xavier, Marilia B., Haslett, Patrick A., Nixon, Douglas F., Kallas, Esper G. [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
dARK ID: ark:/48912/001300000nk6m
Texto Completo: http://dx.doi.org/10.1111/j.1365-2567.2012.03563.x
http://repositorio.unifesp.br/handle/11600/34819
Resumo: Natural killer T (NKT) cells are a heterogeneous population of lymphocytes that recognize antigens presented by CD1d and have attracted attention because of their potential role linking innate and adaptive immune responses. Peripheral NKT cells display a memory-activated phenotype and can rapidly secrete large amounts of pro-inflammatory cytokines upon antigenic activation. in this study, we evaluated NKT cells in the context of patients co-infected with HIV-1 and Mycobacterium leprae. the volunteers were enrolled into four groups: 22 healthy controls, 23 HIV-1-infected patients, 20 patients with leprosy and 17 patients with leprosy and HIV-1-infection. Flow cytometry and ELISPOT assays were performed on peripheral blood mononuclear cells. We demonstrated that patients co-infected with HIV-1 and M.leprae have significantly lower NKT cell frequencies [median 0.022%, interquartile range (IQR): 0.0070.051] in the peripheral blood when compared with healthy subjects (median 0.077%, IQR: 0.0320.405, P < 0.01) or HIV-1 mono-infected patients (median 0.072%, IQR: 0.0300.160, P < 0.05). Also, more NKT cells from co-infected patients secreted interferon-? after stimulation with DimerX, when compared with leprosy mono-infected patients (P = 0.05). These results suggest that NKT cells are decreased in frequency in HIV-1 and M.leprae co-infected patients compared with HIV-1 mono-infected patients alone, but are at a more activated state. Innate immunity in human subjects is strongly influenced by their spectrum of chronic infections, and in HIV-1-infected subjects, a concurrent mycobacterial infection probably hyper-activates and lowers circulating NKT cell numbers.
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spelling Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patientsco-infectionHIV-1interferon-leprosyMycobacterium lepraenatural killer T cellNatural killer T (NKT) cells are a heterogeneous population of lymphocytes that recognize antigens presented by CD1d and have attracted attention because of their potential role linking innate and adaptive immune responses. Peripheral NKT cells display a memory-activated phenotype and can rapidly secrete large amounts of pro-inflammatory cytokines upon antigenic activation. in this study, we evaluated NKT cells in the context of patients co-infected with HIV-1 and Mycobacterium leprae. the volunteers were enrolled into four groups: 22 healthy controls, 23 HIV-1-infected patients, 20 patients with leprosy and 17 patients with leprosy and HIV-1-infection. Flow cytometry and ELISPOT assays were performed on peripheral blood mononuclear cells. We demonstrated that patients co-infected with HIV-1 and M.leprae have significantly lower NKT cell frequencies [median 0.022%, interquartile range (IQR): 0.0070.051] in the peripheral blood when compared with healthy subjects (median 0.077%, IQR: 0.0320.405, P < 0.01) or HIV-1 mono-infected patients (median 0.072%, IQR: 0.0300.160, P < 0.05). Also, more NKT cells from co-infected patients secreted interferon-? after stimulation with DimerX, when compared with leprosy mono-infected patients (P = 0.05). These results suggest that NKT cells are decreased in frequency in HIV-1 and M.leprae co-infected patients compared with HIV-1 mono-infected patients alone, but are at a more activated state. Innate immunity in human subjects is strongly influenced by their spectrum of chronic infections, and in HIV-1-infected subjects, a concurrent mycobacterial infection probably hyper-activates and lowers circulating NKT cell numbers.Univ São Paulo, Lab Invest Med 60, Div Clin Immunol & Allergy, BR-01246903 São Paulo, BrazilUniv Calif San Francisco, San Francisco Gen Hosp, Dept Med, Div Expt Med, San Francisco, CA USAUniversidade Federal de São Paulo, São Paulo, BrazilFed Univ Para, BR-66059 Belem, Para, BrazilShire Human Genet Therapies, Lexington, MA USAUniversidade Federal de São Paulo, São Paulo, BrazilWeb of ScienceNational Institutes of HealthFogarty International CenterFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Brazilian Ministry of Science and TechnologyNew York Community TrustNational Institutes of Health: R01-AI52731National Institutes of Health: AI060379Fogarty International Center: D43 TW00003FAPESP: 04/15856-9/KallasFAPESP: 2010/05845-0/KallasBrazilian Ministry of Science and Technology: 484230/2011-5Wiley-BlackwellUniversidade de São Paulo (USP)Univ Calif San FranciscoUniversidade Federal de São Paulo (UNIFESP)Fed Univ ParaShire Human Genet TherapiesCarvalho, Karina I.Bruno, Fernanda R.Snyder-Cappione, Jennifer E.Maeda, Solange M. [UNIFESP]Tomimori, Jane [UNIFESP]Xavier, Marilia B.Haslett, Patrick A.Nixon, Douglas F.Kallas, Esper G. [UNIFESP]2016-01-24T14:27:08Z2016-01-24T14:27:08Z2012-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion96-102http://dx.doi.org/10.1111/j.1365-2567.2012.03563.xImmunology. Malden: Wiley-Blackwell, v. 136, n. 1, p. 96-102, 2012.10.1111/j.1365-2567.2012.03563.x0019-2805http://repositorio.unifesp.br/handle/11600/34819WOS:000302399200011ark:/48912/001300000nk6mengImmunologyinfo:eu-repo/semantics/openAccesshttp://olabout.wiley.com/WileyCDA/Section/id-406071.htmlreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T12:27:08Zoai:repositorio.unifesp.br/:11600/34819Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:27:21.144561Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients
title Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients
spellingShingle Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients
Carvalho, Karina I.
co-infection
HIV-1
interferon-
leprosy
Mycobacterium leprae
natural killer T cell
title_short Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients
title_full Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients
title_fullStr Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients
title_full_unstemmed Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients
title_sort Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients
author Carvalho, Karina I.
author_facet Carvalho, Karina I.
Bruno, Fernanda R.
Snyder-Cappione, Jennifer E.
Maeda, Solange M. [UNIFESP]
Tomimori, Jane [UNIFESP]
Xavier, Marilia B.
Haslett, Patrick A.
Nixon, Douglas F.
Kallas, Esper G. [UNIFESP]
author_role author
author2 Bruno, Fernanda R.
Snyder-Cappione, Jennifer E.
Maeda, Solange M. [UNIFESP]
Tomimori, Jane [UNIFESP]
Xavier, Marilia B.
Haslett, Patrick A.
Nixon, Douglas F.
Kallas, Esper G. [UNIFESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Univ Calif San Francisco
Universidade Federal de São Paulo (UNIFESP)
Fed Univ Para
Shire Human Genet Therapies
dc.contributor.author.fl_str_mv Carvalho, Karina I.
Bruno, Fernanda R.
Snyder-Cappione, Jennifer E.
Maeda, Solange M. [UNIFESP]
Tomimori, Jane [UNIFESP]
Xavier, Marilia B.
Haslett, Patrick A.
Nixon, Douglas F.
Kallas, Esper G. [UNIFESP]
dc.subject.por.fl_str_mv co-infection
HIV-1
interferon-
leprosy
Mycobacterium leprae
natural killer T cell
topic co-infection
HIV-1
interferon-
leprosy
Mycobacterium leprae
natural killer T cell
description Natural killer T (NKT) cells are a heterogeneous population of lymphocytes that recognize antigens presented by CD1d and have attracted attention because of their potential role linking innate and adaptive immune responses. Peripheral NKT cells display a memory-activated phenotype and can rapidly secrete large amounts of pro-inflammatory cytokines upon antigenic activation. in this study, we evaluated NKT cells in the context of patients co-infected with HIV-1 and Mycobacterium leprae. the volunteers were enrolled into four groups: 22 healthy controls, 23 HIV-1-infected patients, 20 patients with leprosy and 17 patients with leprosy and HIV-1-infection. Flow cytometry and ELISPOT assays were performed on peripheral blood mononuclear cells. We demonstrated that patients co-infected with HIV-1 and M.leprae have significantly lower NKT cell frequencies [median 0.022%, interquartile range (IQR): 0.0070.051] in the peripheral blood when compared with healthy subjects (median 0.077%, IQR: 0.0320.405, P < 0.01) or HIV-1 mono-infected patients (median 0.072%, IQR: 0.0300.160, P < 0.05). Also, more NKT cells from co-infected patients secreted interferon-? after stimulation with DimerX, when compared with leprosy mono-infected patients (P = 0.05). These results suggest that NKT cells are decreased in frequency in HIV-1 and M.leprae co-infected patients compared with HIV-1 mono-infected patients alone, but are at a more activated state. Innate immunity in human subjects is strongly influenced by their spectrum of chronic infections, and in HIV-1-infected subjects, a concurrent mycobacterial infection probably hyper-activates and lowers circulating NKT cell numbers.
publishDate 2012
dc.date.none.fl_str_mv 2012-05-01
2016-01-24T14:27:08Z
2016-01-24T14:27:08Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1111/j.1365-2567.2012.03563.x
Immunology. Malden: Wiley-Blackwell, v. 136, n. 1, p. 96-102, 2012.
10.1111/j.1365-2567.2012.03563.x
0019-2805
http://repositorio.unifesp.br/handle/11600/34819
WOS:000302399200011
dc.identifier.dark.fl_str_mv ark:/48912/001300000nk6m
url http://dx.doi.org/10.1111/j.1365-2567.2012.03563.x
http://repositorio.unifesp.br/handle/11600/34819
identifier_str_mv Immunology. Malden: Wiley-Blackwell, v. 136, n. 1, p. 96-102, 2012.
10.1111/j.1365-2567.2012.03563.x
0019-2805
WOS:000302399200011
ark:/48912/001300000nk6m
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Immunology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://olabout.wiley.com/WileyCDA/Section/id-406071.html
eu_rights_str_mv openAccess
rights_invalid_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
dc.format.none.fl_str_mv 96-102
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 biblioteca.csp@unifesp.br
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