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Protective Response in Experimental Paracoccidioidomycosis Elicited by Extracellular Vesicles Containing Antigens of Paracoccidioides brasiliensis
Paracoccidioidomycosis (PCM) is a systemic disease caused by Paracoccidioides spp. PCM is endemic in Latin America and most cases are registered in Brazil. This mycosis affects mainly the lungs, but can also spread to other tissues and organs, including the liver. Several approaches have been invest...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304155/ https://www.ncbi.nlm.nih.gov/pubmed/34359982 http://dx.doi.org/10.3390/cells10071813 |
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author | Baltazar, Ludmila Matos Ribeiro, Gabriela Fior Freitas, Gustavo J. Queiroz-Junior, Celso Martins Fagundes, Caio Tavares Chaves-Olórtegui, Carlos Teixeira, Mauro Martins Souza, Daniele G. |
author_facet | Baltazar, Ludmila Matos Ribeiro, Gabriela Fior Freitas, Gustavo J. Queiroz-Junior, Celso Martins Fagundes, Caio Tavares Chaves-Olórtegui, Carlos Teixeira, Mauro Martins Souza, Daniele G. |
author_sort | Baltazar, Ludmila Matos |
collection | PubMed |
description | Paracoccidioidomycosis (PCM) is a systemic disease caused by Paracoccidioides spp. PCM is endemic in Latin America and most cases are registered in Brazil. This mycosis affects mainly the lungs, but can also spread to other tissues and organs, including the liver. Several approaches have been investigated to improve treatment effectiveness and protection against the disease. Extracellular vesicles (EVs) are good antigen delivery vehicles. The present work aims to investigate the use of EVs derived from Paracoccidioides brasiliensis as an immunization tool in a murine model of PCM. For this, male C57BL/6 were immunized with two doses of EVs plus adjuvant and then infected with P. brasiliensis. EV immunization induced IgM and IgG in vivo and cytokine production by splenocytes ex vivo. Further, immunization with EVs had a positive effect on mice infected with P. brasiliensis, as it induced activated T lymphocytes and NKT cell mobilization to the infected lungs, improved production of proinflammatory cytokines and the histopathological profile, and reduced fungal burden. Therefore, the present study shows a new role for P. brasiliensis EVs in the presence of adjuvant as modulators of the host immune system, suggesting their utility as immunizing agents. |
format | Online Article Text |
id | pubmed-8304155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83041552021-07-25 Protective Response in Experimental Paracoccidioidomycosis Elicited by Extracellular Vesicles Containing Antigens of Paracoccidioides brasiliensis Baltazar, Ludmila Matos Ribeiro, Gabriela Fior Freitas, Gustavo J. Queiroz-Junior, Celso Martins Fagundes, Caio Tavares Chaves-Olórtegui, Carlos Teixeira, Mauro Martins Souza, Daniele G. Cells Article Paracoccidioidomycosis (PCM) is a systemic disease caused by Paracoccidioides spp. PCM is endemic in Latin America and most cases are registered in Brazil. This mycosis affects mainly the lungs, but can also spread to other tissues and organs, including the liver. Several approaches have been investigated to improve treatment effectiveness and protection against the disease. Extracellular vesicles (EVs) are good antigen delivery vehicles. The present work aims to investigate the use of EVs derived from Paracoccidioides brasiliensis as an immunization tool in a murine model of PCM. For this, male C57BL/6 were immunized with two doses of EVs plus adjuvant and then infected with P. brasiliensis. EV immunization induced IgM and IgG in vivo and cytokine production by splenocytes ex vivo. Further, immunization with EVs had a positive effect on mice infected with P. brasiliensis, as it induced activated T lymphocytes and NKT cell mobilization to the infected lungs, improved production of proinflammatory cytokines and the histopathological profile, and reduced fungal burden. Therefore, the present study shows a new role for P. brasiliensis EVs in the presence of adjuvant as modulators of the host immune system, suggesting their utility as immunizing agents. MDPI 2021-07-17 /pmc/articles/PMC8304155/ /pubmed/34359982 http://dx.doi.org/10.3390/cells10071813 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Baltazar, Ludmila Matos Ribeiro, Gabriela Fior Freitas, Gustavo J. Queiroz-Junior, Celso Martins Fagundes, Caio Tavares Chaves-Olórtegui, Carlos Teixeira, Mauro Martins Souza, Daniele G. Protective Response in Experimental Paracoccidioidomycosis Elicited by Extracellular Vesicles Containing Antigens of Paracoccidioides brasiliensis |
title | Protective Response in Experimental Paracoccidioidomycosis Elicited by Extracellular Vesicles Containing Antigens of Paracoccidioides brasiliensis |
title_full | Protective Response in Experimental Paracoccidioidomycosis Elicited by Extracellular Vesicles Containing Antigens of Paracoccidioides brasiliensis |
title_fullStr | Protective Response in Experimental Paracoccidioidomycosis Elicited by Extracellular Vesicles Containing Antigens of Paracoccidioides brasiliensis |
title_full_unstemmed | Protective Response in Experimental Paracoccidioidomycosis Elicited by Extracellular Vesicles Containing Antigens of Paracoccidioides brasiliensis |
title_short | Protective Response in Experimental Paracoccidioidomycosis Elicited by Extracellular Vesicles Containing Antigens of Paracoccidioides brasiliensis |
title_sort | protective response in experimental paracoccidioidomycosis elicited by extracellular vesicles containing antigens of paracoccidioides brasiliensis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304155/ https://www.ncbi.nlm.nih.gov/pubmed/34359982 http://dx.doi.org/10.3390/cells10071813 |
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