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In vitro lymphoproliferative response and cytokine production in mice with experimental disseminated candidiasis

OBJECTIVE(S): Systemic candidiasis is an infection of Candida albicans (C. albicans) causing disseminated disease and sepsis, invariably when host defenses are compromised. We investigated the histopathological changes as well as the lymphoproliferative responses and cytokine production of splenic c...

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Autores principales: Khosravi, Ali Reza, Shokri, Hojjatollah, Eshghi, Shahin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339661/
https://www.ncbi.nlm.nih.gov/pubmed/28293397
http://dx.doi.org/10.22038/ijbms.2017.8248
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author Khosravi, Ali Reza
Shokri, Hojjatollah
Eshghi, Shahin
author_facet Khosravi, Ali Reza
Shokri, Hojjatollah
Eshghi, Shahin
author_sort Khosravi, Ali Reza
collection PubMed
description OBJECTIVE(S): Systemic candidiasis is an infection of Candida albicans (C. albicans) causing disseminated disease and sepsis, invariably when host defenses are compromised. We investigated the histopathological changes as well as the lymphoproliferative responses and cytokine production of splenic cells after stimulation with Concanavalin A (Con A) and Pokeweed mitogen (PWM) in mice with disseminated candidiasis. MATERIALS AND METHODS: Lymphoproliferative responses were stimulated in vitro with Con A (1 µg/ml) and PWM (1 µg/ml) mitogens in Roswell Park Memorial Institute (RPMI) 1640 media, and the production of interferon (IFN)-γ and interleukin-4 (IL-4) in the supernatants was measured by enzyme-linked immunosorbent assay (ELISA). RESULTS: The results revealed that C. albicans organisms multiplied to a greater extent in the kidneys than in the liver and spleen of infected mice. The most predominant forms of C. albicans in different parts of the kidneys were yeast mixed with hyphal forms. Infected mice had a significantly increased proliferative response when splenocytes were stimulated with PWM (2.0±0.16) and Con A (1.9±0.19) (P<0.05). PWM and Con A-stimulated production of IFN-γ significantly tended to be higher in infected mice (PWM: 68.4±14.0 pg/ml; Con A: 53.7±17.3 pg/ml) when compared to controls (P<0.05). Stimulation with PWM and Con A showed no differences in IL-4 production between infected mice and controls. CONCLUSION: These findings demonstrated a significant increase in both cell proliferation and IFN-γ secretion in supernatants of PWM and Con A- stimulated splenocyte cultures obtained from mice with disseminated candidiasis.
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spelling pubmed-53396612017-03-14 In vitro lymphoproliferative response and cytokine production in mice with experimental disseminated candidiasis Khosravi, Ali Reza Shokri, Hojjatollah Eshghi, Shahin Iran J Basic Med Sci Original Article OBJECTIVE(S): Systemic candidiasis is an infection of Candida albicans (C. albicans) causing disseminated disease and sepsis, invariably when host defenses are compromised. We investigated the histopathological changes as well as the lymphoproliferative responses and cytokine production of splenic cells after stimulation with Concanavalin A (Con A) and Pokeweed mitogen (PWM) in mice with disseminated candidiasis. MATERIALS AND METHODS: Lymphoproliferative responses were stimulated in vitro with Con A (1 µg/ml) and PWM (1 µg/ml) mitogens in Roswell Park Memorial Institute (RPMI) 1640 media, and the production of interferon (IFN)-γ and interleukin-4 (IL-4) in the supernatants was measured by enzyme-linked immunosorbent assay (ELISA). RESULTS: The results revealed that C. albicans organisms multiplied to a greater extent in the kidneys than in the liver and spleen of infected mice. The most predominant forms of C. albicans in different parts of the kidneys were yeast mixed with hyphal forms. Infected mice had a significantly increased proliferative response when splenocytes were stimulated with PWM (2.0±0.16) and Con A (1.9±0.19) (P<0.05). PWM and Con A-stimulated production of IFN-γ significantly tended to be higher in infected mice (PWM: 68.4±14.0 pg/ml; Con A: 53.7±17.3 pg/ml) when compared to controls (P<0.05). Stimulation with PWM and Con A showed no differences in IL-4 production between infected mice and controls. CONCLUSION: These findings demonstrated a significant increase in both cell proliferation and IFN-γ secretion in supernatants of PWM and Con A- stimulated splenocyte cultures obtained from mice with disseminated candidiasis. Mashhad University of Medical Sciences 2017-02 /pmc/articles/PMC5339661/ /pubmed/28293397 http://dx.doi.org/10.22038/ijbms.2017.8248 Text en Copyright: © Iranian Journal of Basic Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Khosravi, Ali Reza
Shokri, Hojjatollah
Eshghi, Shahin
In vitro lymphoproliferative response and cytokine production in mice with experimental disseminated candidiasis
title In vitro lymphoproliferative response and cytokine production in mice with experimental disseminated candidiasis
title_full In vitro lymphoproliferative response and cytokine production in mice with experimental disseminated candidiasis
title_fullStr In vitro lymphoproliferative response and cytokine production in mice with experimental disseminated candidiasis
title_full_unstemmed In vitro lymphoproliferative response and cytokine production in mice with experimental disseminated candidiasis
title_short In vitro lymphoproliferative response and cytokine production in mice with experimental disseminated candidiasis
title_sort in vitro lymphoproliferative response and cytokine production in mice with experimental disseminated candidiasis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339661/
https://www.ncbi.nlm.nih.gov/pubmed/28293397
http://dx.doi.org/10.22038/ijbms.2017.8248
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