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Antibody Therapy for Histoplasmosis
The endemic human pathogenic fungus Histoplasma capsulatum is a major fungal pathogen with a broad variety of clinical presentations, ranging from mild, focal pulmonary disease to life-threatening systemic infections. Although azoles, such as itraconazole and voriconazole, and amphotericin B have si...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3270318/ https://www.ncbi.nlm.nih.gov/pubmed/22347215 http://dx.doi.org/10.3389/fmicb.2012.00021 |
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author | Nosanchuk, Joshua D. Zancopé-Oliveira, Rosely M. Hamilton, Andrew J. Guimarães, Allan J. |
author_facet | Nosanchuk, Joshua D. Zancopé-Oliveira, Rosely M. Hamilton, Andrew J. Guimarães, Allan J. |
author_sort | Nosanchuk, Joshua D. |
collection | PubMed |
description | The endemic human pathogenic fungus Histoplasma capsulatum is a major fungal pathogen with a broad variety of clinical presentations, ranging from mild, focal pulmonary disease to life-threatening systemic infections. Although azoles, such as itraconazole and voriconazole, and amphotericin B have significant activity against H. capsulatum, about 1 in 10 patients hospitalized due to histoplasmosis die. Hence, new approaches for managing disease are being sought. Over the past 10 years, studies have demonstrated that monoclonal antibodies (mAbs) can modify the pathogenesis of histoplasmosis. Disease has been shown to be impacted by mAbs targeting either fungal cell surface proteins or host co-stimulatory molecules. This review will detail our current knowledge regarding the impact of antibody therapy on histoplasmosis. |
format | Online Article Text |
id | pubmed-3270318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32703182012-02-15 Antibody Therapy for Histoplasmosis Nosanchuk, Joshua D. Zancopé-Oliveira, Rosely M. Hamilton, Andrew J. Guimarães, Allan J. Front Microbiol Microbiology The endemic human pathogenic fungus Histoplasma capsulatum is a major fungal pathogen with a broad variety of clinical presentations, ranging from mild, focal pulmonary disease to life-threatening systemic infections. Although azoles, such as itraconazole and voriconazole, and amphotericin B have significant activity against H. capsulatum, about 1 in 10 patients hospitalized due to histoplasmosis die. Hence, new approaches for managing disease are being sought. Over the past 10 years, studies have demonstrated that monoclonal antibodies (mAbs) can modify the pathogenesis of histoplasmosis. Disease has been shown to be impacted by mAbs targeting either fungal cell surface proteins or host co-stimulatory molecules. This review will detail our current knowledge regarding the impact of antibody therapy on histoplasmosis. Frontiers Research Foundation 2012-02-02 /pmc/articles/PMC3270318/ /pubmed/22347215 http://dx.doi.org/10.3389/fmicb.2012.00021 Text en Copyright © 2012 Nosanchuk, Zancopé-Oliveira, Hamilton and Guimarães. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Microbiology Nosanchuk, Joshua D. Zancopé-Oliveira, Rosely M. Hamilton, Andrew J. Guimarães, Allan J. Antibody Therapy for Histoplasmosis |
title | Antibody Therapy for Histoplasmosis |
title_full | Antibody Therapy for Histoplasmosis |
title_fullStr | Antibody Therapy for Histoplasmosis |
title_full_unstemmed | Antibody Therapy for Histoplasmosis |
title_short | Antibody Therapy for Histoplasmosis |
title_sort | antibody therapy for histoplasmosis |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3270318/ https://www.ncbi.nlm.nih.gov/pubmed/22347215 http://dx.doi.org/10.3389/fmicb.2012.00021 |
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