Cargando…

T Helper 1–Inducing Adjuvant Protects against Experimental Paracoccidioidomycosis

Immunostimulatory therapy is a promising approach to improving the treatment of systemic fungal infections such as paracoccidioidomycosis (PCM), whose drug therapy is usually prolonged and associated with toxic side effects and relapses. The current study was undertaken to determine if the injection...

Descripción completa

Detalles Bibliográficos
Autores principales: de Oliveira, Leandro Licursi, Coltri, Kely Cristine, Cardoso, Cristina Ribeiro Barros, Roque-Barreira, Maria-Cristina, Panunto-Castelo, Ademilson
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2263123/
https://www.ncbi.nlm.nih.gov/pubmed/18335066
http://dx.doi.org/10.1371/journal.pntd.0000183
_version_ 1782151444077477888
author de Oliveira, Leandro Licursi
Coltri, Kely Cristine
Cardoso, Cristina Ribeiro Barros
Roque-Barreira, Maria-Cristina
Panunto-Castelo, Ademilson
author_facet de Oliveira, Leandro Licursi
Coltri, Kely Cristine
Cardoso, Cristina Ribeiro Barros
Roque-Barreira, Maria-Cristina
Panunto-Castelo, Ademilson
author_sort de Oliveira, Leandro Licursi
collection PubMed
description Immunostimulatory therapy is a promising approach to improving the treatment of systemic fungal infections such as paracoccidioidomycosis (PCM), whose drug therapy is usually prolonged and associated with toxic side effects and relapses. The current study was undertaken to determine if the injection of a T helper (Th) 1–stimulating adjuvant in P. brasiliensis–infected mice could have a beneficial effect on the course of experimental PCM. For this purpose, mice were infected and treated with complete Freund's adjuvant (CFA), a well-established Th1 experimental inductor, or incomplete Freund's adjuvant (IFA - control group) on day 20 postinfection. Four weeks after treatment, the CFA-treated mice presented a mild infection in the lungs characterized by absence of epithelioid cell granulomas and yeast cells, whereas the control mice presented multiple sites of focal epithelioid granulomas with lymphomonocytic halos circumscribing a high number of viable and nonviable yeast cells. In addition, CFA administration induced a 2.4 log reduction (>99%) in the fungal burden when compared to the control group, and led to an improvement of immune response, reversing the immunosuppression observed in the control group. The immunotherapy with Th1-inducing adjuvant, approved to be used in humans, might be a valuable tool in the treatment of PCM and potentially useful to improve the clinical cure rate in humans.
format Text
id pubmed-2263123
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-22631232008-03-12 T Helper 1–Inducing Adjuvant Protects against Experimental Paracoccidioidomycosis de Oliveira, Leandro Licursi Coltri, Kely Cristine Cardoso, Cristina Ribeiro Barros Roque-Barreira, Maria-Cristina Panunto-Castelo, Ademilson PLoS Negl Trop Dis Research Article Immunostimulatory therapy is a promising approach to improving the treatment of systemic fungal infections such as paracoccidioidomycosis (PCM), whose drug therapy is usually prolonged and associated with toxic side effects and relapses. The current study was undertaken to determine if the injection of a T helper (Th) 1–stimulating adjuvant in P. brasiliensis–infected mice could have a beneficial effect on the course of experimental PCM. For this purpose, mice were infected and treated with complete Freund's adjuvant (CFA), a well-established Th1 experimental inductor, or incomplete Freund's adjuvant (IFA - control group) on day 20 postinfection. Four weeks after treatment, the CFA-treated mice presented a mild infection in the lungs characterized by absence of epithelioid cell granulomas and yeast cells, whereas the control mice presented multiple sites of focal epithelioid granulomas with lymphomonocytic halos circumscribing a high number of viable and nonviable yeast cells. In addition, CFA administration induced a 2.4 log reduction (>99%) in the fungal burden when compared to the control group, and led to an improvement of immune response, reversing the immunosuppression observed in the control group. The immunotherapy with Th1-inducing adjuvant, approved to be used in humans, might be a valuable tool in the treatment of PCM and potentially useful to improve the clinical cure rate in humans. Public Library of Science 2008-03-12 /pmc/articles/PMC2263123/ /pubmed/18335066 http://dx.doi.org/10.1371/journal.pntd.0000183 Text en de Oliveira 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
de Oliveira, Leandro Licursi
Coltri, Kely Cristine
Cardoso, Cristina Ribeiro Barros
Roque-Barreira, Maria-Cristina
Panunto-Castelo, Ademilson
T Helper 1–Inducing Adjuvant Protects against Experimental Paracoccidioidomycosis
title T Helper 1–Inducing Adjuvant Protects against Experimental Paracoccidioidomycosis
title_full T Helper 1–Inducing Adjuvant Protects against Experimental Paracoccidioidomycosis
title_fullStr T Helper 1–Inducing Adjuvant Protects against Experimental Paracoccidioidomycosis
title_full_unstemmed T Helper 1–Inducing Adjuvant Protects against Experimental Paracoccidioidomycosis
title_short T Helper 1–Inducing Adjuvant Protects against Experimental Paracoccidioidomycosis
title_sort t helper 1–inducing adjuvant protects against experimental paracoccidioidomycosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2263123/
https://www.ncbi.nlm.nih.gov/pubmed/18335066
http://dx.doi.org/10.1371/journal.pntd.0000183
work_keys_str_mv AT deoliveiraleandrolicursi thelper1inducingadjuvantprotectsagainstexperimentalparacoccidioidomycosis
AT coltrikelycristine thelper1inducingadjuvantprotectsagainstexperimentalparacoccidioidomycosis
AT cardosocristinaribeirobarros thelper1inducingadjuvantprotectsagainstexperimentalparacoccidioidomycosis
AT roquebarreiramariacristina thelper1inducingadjuvantprotectsagainstexperimentalparacoccidioidomycosis
AT panuntocasteloademilson thelper1inducingadjuvantprotectsagainstexperimentalparacoccidioidomycosis