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Cytokine patterns in a prospective cohort of HIV-infected patients with cryptococcal meningitis following initiation of antifungal and antiretroviral therapy

Cryptococcal meningitis (CM) is a life-threatening infection in HIV-infected patients, especially in resource-limited settings. Cytokine patterns in the cerebrospinal fluid (CSF) and sera may be related to clinical outcomes. This study aimed to evaluate cytokine patterns in the CSF and sera of HIV-i...

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Autores principales: Mora, Delio José, Ferreira-Paim, Kennio, Andrade-Silva, Leonardo Eurípedes, Bragine, Thatiane, Rocha, Ivonete Helena, Ribeiro, Barbara de Melo, Machado, Guilherme Henrique, Rodrigues Junior, Virmondes, Silva-Teixeira, David Nascimento, Meyer, Wieland, Silva-Vergara, Mario León
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423598/
https://www.ncbi.nlm.nih.gov/pubmed/28486489
http://dx.doi.org/10.1371/journal.pone.0176304
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author Mora, Delio José
Ferreira-Paim, Kennio
Andrade-Silva, Leonardo Eurípedes
Bragine, Thatiane
Rocha, Ivonete Helena
Ribeiro, Barbara de Melo
Machado, Guilherme Henrique
Rodrigues Junior, Virmondes
Silva-Teixeira, David Nascimento
Meyer, Wieland
Silva-Vergara, Mario León
author_facet Mora, Delio José
Ferreira-Paim, Kennio
Andrade-Silva, Leonardo Eurípedes
Bragine, Thatiane
Rocha, Ivonete Helena
Ribeiro, Barbara de Melo
Machado, Guilherme Henrique
Rodrigues Junior, Virmondes
Silva-Teixeira, David Nascimento
Meyer, Wieland
Silva-Vergara, Mario León
author_sort Mora, Delio José
collection PubMed
description Cryptococcal meningitis (CM) is a life-threatening infection in HIV-infected patients, especially in resource-limited settings. Cytokine patterns in the cerebrospinal fluid (CSF) and sera may be related to clinical outcomes. This study aimed to evaluate cytokine patterns in the CSF and sera of HIV-infected patients with CM as well as the cytokines produced by peripheral blood mononuclear cells (PBMCs) when stimulated with LPS and cryptococcal GXM. CSF and serum levels of IL-2, IL-4, IL-8, IL-10, IL-12p40, IL-17A, INF-γ, TNF-α and CXCL-10 were measured in HIV-infected patients with CM (CM(+) HIV(+)) at various time points. Cytokine levels were evaluated in the PBMC culture supernatants and the baseline values were compared to those of HIV-infected patients without CM (CM(-) HIV(+)) and healthy controls (CM(-) HIV(-)). CSF cytokine levels at admission (n = 33) were higher than levels among the 23 survivors at week 2, but statistically significant differences were observed for IL-8 and IFN-γ (p<0.05). CSF and serum levels of IL-4 and IL-17A at week 10 (n = 16) were lower than the baseline values, whereas IL-2 levels increased compared to week 2 (p<0.05). At week 16 (n = 15), CSF and serum levels of IL-4, IL-10 and CXCL-10 were decreased compared to the baseline values (p<0.05). PBMCs from CM(-) HIV(-) individuals produced significantly higher levels of proinflammatory cytokines in response to LPS, with the exception of TNF-α, which showed higher levels among CM(+) HIV(+) patients. The PBMCs of CM patients produced higher levels of IL-4 than those of CM(-) HIV(-) patients in response to GXM stimulation, and levels progressively decreased during treatment (p<0.05). Then, a progressive shift in cytokine expression favoring a Th1 pattern was observed, which is crucial in controlling cryptococcal infection. A better understanding of the protective immune response against Cryptococcus neoformans will help to develop novel strategies to improve the outcomes of patients with cryptococcosis.
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spelling pubmed-54235982017-05-15 Cytokine patterns in a prospective cohort of HIV-infected patients with cryptococcal meningitis following initiation of antifungal and antiretroviral therapy Mora, Delio José Ferreira-Paim, Kennio Andrade-Silva, Leonardo Eurípedes Bragine, Thatiane Rocha, Ivonete Helena Ribeiro, Barbara de Melo Machado, Guilherme Henrique Rodrigues Junior, Virmondes Silva-Teixeira, David Nascimento Meyer, Wieland Silva-Vergara, Mario León PLoS One Research Article Cryptococcal meningitis (CM) is a life-threatening infection in HIV-infected patients, especially in resource-limited settings. Cytokine patterns in the cerebrospinal fluid (CSF) and sera may be related to clinical outcomes. This study aimed to evaluate cytokine patterns in the CSF and sera of HIV-infected patients with CM as well as the cytokines produced by peripheral blood mononuclear cells (PBMCs) when stimulated with LPS and cryptococcal GXM. CSF and serum levels of IL-2, IL-4, IL-8, IL-10, IL-12p40, IL-17A, INF-γ, TNF-α and CXCL-10 were measured in HIV-infected patients with CM (CM(+) HIV(+)) at various time points. Cytokine levels were evaluated in the PBMC culture supernatants and the baseline values were compared to those of HIV-infected patients without CM (CM(-) HIV(+)) and healthy controls (CM(-) HIV(-)). CSF cytokine levels at admission (n = 33) were higher than levels among the 23 survivors at week 2, but statistically significant differences were observed for IL-8 and IFN-γ (p<0.05). CSF and serum levels of IL-4 and IL-17A at week 10 (n = 16) were lower than the baseline values, whereas IL-2 levels increased compared to week 2 (p<0.05). At week 16 (n = 15), CSF and serum levels of IL-4, IL-10 and CXCL-10 were decreased compared to the baseline values (p<0.05). PBMCs from CM(-) HIV(-) individuals produced significantly higher levels of proinflammatory cytokines in response to LPS, with the exception of TNF-α, which showed higher levels among CM(+) HIV(+) patients. The PBMCs of CM patients produced higher levels of IL-4 than those of CM(-) HIV(-) patients in response to GXM stimulation, and levels progressively decreased during treatment (p<0.05). Then, a progressive shift in cytokine expression favoring a Th1 pattern was observed, which is crucial in controlling cryptococcal infection. A better understanding of the protective immune response against Cryptococcus neoformans will help to develop novel strategies to improve the outcomes of patients with cryptococcosis. Public Library of Science 2017-05-09 /pmc/articles/PMC5423598/ /pubmed/28486489 http://dx.doi.org/10.1371/journal.pone.0176304 Text en © 2017 Mora et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Mora, Delio José
Ferreira-Paim, Kennio
Andrade-Silva, Leonardo Eurípedes
Bragine, Thatiane
Rocha, Ivonete Helena
Ribeiro, Barbara de Melo
Machado, Guilherme Henrique
Rodrigues Junior, Virmondes
Silva-Teixeira, David Nascimento
Meyer, Wieland
Silva-Vergara, Mario León
Cytokine patterns in a prospective cohort of HIV-infected patients with cryptococcal meningitis following initiation of antifungal and antiretroviral therapy
title Cytokine patterns in a prospective cohort of HIV-infected patients with cryptococcal meningitis following initiation of antifungal and antiretroviral therapy
title_full Cytokine patterns in a prospective cohort of HIV-infected patients with cryptococcal meningitis following initiation of antifungal and antiretroviral therapy
title_fullStr Cytokine patterns in a prospective cohort of HIV-infected patients with cryptococcal meningitis following initiation of antifungal and antiretroviral therapy
title_full_unstemmed Cytokine patterns in a prospective cohort of HIV-infected patients with cryptococcal meningitis following initiation of antifungal and antiretroviral therapy
title_short Cytokine patterns in a prospective cohort of HIV-infected patients with cryptococcal meningitis following initiation of antifungal and antiretroviral therapy
title_sort cytokine patterns in a prospective cohort of hiv-infected patients with cryptococcal meningitis following initiation of antifungal and antiretroviral therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423598/
https://www.ncbi.nlm.nih.gov/pubmed/28486489
http://dx.doi.org/10.1371/journal.pone.0176304
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