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The Role of Cryptococcus in the Immune System of Pulmonary Cryptococcosis Patients

OBJECTIVES: To investigate the role of Cryptococcus in the immune system of immunocompetent patients with pulmonary cryptococcosis (PC) by analysing the dynamic changes of patients’ immune status before and after antifungal therapy. METHODS: The level of the serum interferon-γ (IFN-γ) and interleuki...

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Autores principales: Wang, Jinlin, Zeng, Yunxiang, Luo, Weizhan, Xie, Xiaohong, Li, Shiyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670196/
https://www.ncbi.nlm.nih.gov/pubmed/26637129
http://dx.doi.org/10.1371/journal.pone.0144427
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author Wang, Jinlin
Zeng, Yunxiang
Luo, Weizhan
Xie, Xiaohong
Li, Shiyue
author_facet Wang, Jinlin
Zeng, Yunxiang
Luo, Weizhan
Xie, Xiaohong
Li, Shiyue
author_sort Wang, Jinlin
collection PubMed
description OBJECTIVES: To investigate the role of Cryptococcus in the immune system of immunocompetent patients with pulmonary cryptococcosis (PC) by analysing the dynamic changes of patients’ immune status before and after antifungal therapy. METHODS: The level of the serum interferon-γ (IFN-γ) and interleukin (IL)-2, -4, -10 and -12 was measured before and after 6-months of treatment. Peripheral blood samples were obtained from 30 immunocompetent PC patients and 30 age- and gender-matched healthy controls. Peripheral blood mononuclear cells (PBMCs) were isolated and incubated with recombinant human IL-12 (rhIL-12) for 48 h. Then the concentrations of IFN-γ and IL-4 in the supernatant were analysed. RESULTS: Baseline serum IFN-γ level was significantly lower in the PC patients as compared with the control group (P < 0.001). The serum IL-2 and IFN-γ of PC patients were significantly increased after appropriate treatments (P < 0.05 and P < 0.001 when compared to their baseline levels). The productions of IFN-γ in the culture supernatant of PBMCs showed no significant difference between the control and PC patients both before and after antifungal treatments. RhIL-12 is a potent stimulus for IFN-γ production. Culture PBMCs collected from PC patients before treatments had a smaller increase of IFN-γ production in the present of rhIL-12 than the control (P < 0.01); PBMCs from PC patients completing 6-months of treatment showed a comparable increase of IFN-γ production by rhIL-12 stimulation to the control group. CONCLUSIONS: In apparently immunocompetent patients with PC, a normalization of serum IFN-γ was achieved after recovery from infection. This suggests that Cryptococcus infection per se can suppress the immune system and its elimination contributes to the reestablishment of an immune equilibrium.
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spelling pubmed-46701962015-12-10 The Role of Cryptococcus in the Immune System of Pulmonary Cryptococcosis Patients Wang, Jinlin Zeng, Yunxiang Luo, Weizhan Xie, Xiaohong Li, Shiyue PLoS One Research Article OBJECTIVES: To investigate the role of Cryptococcus in the immune system of immunocompetent patients with pulmonary cryptococcosis (PC) by analysing the dynamic changes of patients’ immune status before and after antifungal therapy. METHODS: The level of the serum interferon-γ (IFN-γ) and interleukin (IL)-2, -4, -10 and -12 was measured before and after 6-months of treatment. Peripheral blood samples were obtained from 30 immunocompetent PC patients and 30 age- and gender-matched healthy controls. Peripheral blood mononuclear cells (PBMCs) were isolated and incubated with recombinant human IL-12 (rhIL-12) for 48 h. Then the concentrations of IFN-γ and IL-4 in the supernatant were analysed. RESULTS: Baseline serum IFN-γ level was significantly lower in the PC patients as compared with the control group (P < 0.001). The serum IL-2 and IFN-γ of PC patients were significantly increased after appropriate treatments (P < 0.05 and P < 0.001 when compared to their baseline levels). The productions of IFN-γ in the culture supernatant of PBMCs showed no significant difference between the control and PC patients both before and after antifungal treatments. RhIL-12 is a potent stimulus for IFN-γ production. Culture PBMCs collected from PC patients before treatments had a smaller increase of IFN-γ production in the present of rhIL-12 than the control (P < 0.01); PBMCs from PC patients completing 6-months of treatment showed a comparable increase of IFN-γ production by rhIL-12 stimulation to the control group. CONCLUSIONS: In apparently immunocompetent patients with PC, a normalization of serum IFN-γ was achieved after recovery from infection. This suggests that Cryptococcus infection per se can suppress the immune system and its elimination contributes to the reestablishment of an immune equilibrium. Public Library of Science 2015-12-04 /pmc/articles/PMC4670196/ /pubmed/26637129 http://dx.doi.org/10.1371/journal.pone.0144427 Text en © 2015 Wang 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wang, Jinlin
Zeng, Yunxiang
Luo, Weizhan
Xie, Xiaohong
Li, Shiyue
The Role of Cryptococcus in the Immune System of Pulmonary Cryptococcosis Patients
title The Role of Cryptococcus in the Immune System of Pulmonary Cryptococcosis Patients
title_full The Role of Cryptococcus in the Immune System of Pulmonary Cryptococcosis Patients
title_fullStr The Role of Cryptococcus in the Immune System of Pulmonary Cryptococcosis Patients
title_full_unstemmed The Role of Cryptococcus in the Immune System of Pulmonary Cryptococcosis Patients
title_short The Role of Cryptococcus in the Immune System of Pulmonary Cryptococcosis Patients
title_sort role of cryptococcus in the immune system of pulmonary cryptococcosis patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670196/
https://www.ncbi.nlm.nih.gov/pubmed/26637129
http://dx.doi.org/10.1371/journal.pone.0144427
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