Lower numbers of natural killer T cells in HIV-1 and Mycobacterium leprae co-infected patients
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , , |
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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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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1818602489921929216 |