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Vaccine-Mediated Immune Responses to Experimental Pulmonary Cryptococcus gattii Infection in Mice
Cryptococcus gattii is a fungal pathogen that can cause life-threatening respiratory and disseminated infections in immune-competent and immune-suppressed individuals. Currently, there are no standardized vaccines against cryptococcosis in humans, underlying an urgent need for effective therapies an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132117/ https://www.ncbi.nlm.nih.gov/pubmed/25119981 http://dx.doi.org/10.1371/journal.pone.0104316 |
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author | Chaturvedi, Ashok K. Hameed, Rumanasma S. Wozniak, Karen L. Hole, Camaron R. Leopold Wager, Chrissy M. Weintraub, Susan T. Lopez-Ribot, Jose L. Wormley, Floyd L. |
author_facet | Chaturvedi, Ashok K. Hameed, Rumanasma S. Wozniak, Karen L. Hole, Camaron R. Leopold Wager, Chrissy M. Weintraub, Susan T. Lopez-Ribot, Jose L. Wormley, Floyd L. |
author_sort | Chaturvedi, Ashok K. |
collection | PubMed |
description | Cryptococcus gattii is a fungal pathogen that can cause life-threatening respiratory and disseminated infections in immune-competent and immune-suppressed individuals. Currently, there are no standardized vaccines against cryptococcosis in humans, underlying an urgent need for effective therapies and/or vaccines. In this study, we evaluated the efficacy of intranasal immunization with C. gattii cell wall associated (CW) and/or cytoplasmic (CP) protein preparations to induce protection against experimental pulmonary C. gattii infection in mice. BALB/c mice immunized with C. gattii CW and/or CP protein preparations exhibited a significant reduction in pulmonary fungal burden and prolonged survival following pulmonary challenge with C. gattii. Protection was associated with significantly increased pro-inflammatory and Th1-type cytokine recall responses, in vitro and increased C. gattii-specific antibody production in immunized mice challenged with C. gattii. A number of immunodominant proteins were identified following immunoblot analysis of C. gattii CW and CP protein preparations using sera from immunized mice. Immunization with a combined CW and CP protein preparation resulted in an early increase in pulmonary T cell infiltrates following challenge with C. gattii. Overall, our studies show that C. gattii CW and CP protein preparations contain antigens that may be included in a subunit vaccine to induce prolonged protection against pulmonary C. gattii infection. |
format | Online Article Text |
id | pubmed-4132117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41321172014-08-19 Vaccine-Mediated Immune Responses to Experimental Pulmonary Cryptococcus gattii Infection in Mice Chaturvedi, Ashok K. Hameed, Rumanasma S. Wozniak, Karen L. Hole, Camaron R. Leopold Wager, Chrissy M. Weintraub, Susan T. Lopez-Ribot, Jose L. Wormley, Floyd L. PLoS One Research Article Cryptococcus gattii is a fungal pathogen that can cause life-threatening respiratory and disseminated infections in immune-competent and immune-suppressed individuals. Currently, there are no standardized vaccines against cryptococcosis in humans, underlying an urgent need for effective therapies and/or vaccines. In this study, we evaluated the efficacy of intranasal immunization with C. gattii cell wall associated (CW) and/or cytoplasmic (CP) protein preparations to induce protection against experimental pulmonary C. gattii infection in mice. BALB/c mice immunized with C. gattii CW and/or CP protein preparations exhibited a significant reduction in pulmonary fungal burden and prolonged survival following pulmonary challenge with C. gattii. Protection was associated with significantly increased pro-inflammatory and Th1-type cytokine recall responses, in vitro and increased C. gattii-specific antibody production in immunized mice challenged with C. gattii. A number of immunodominant proteins were identified following immunoblot analysis of C. gattii CW and CP protein preparations using sera from immunized mice. Immunization with a combined CW and CP protein preparation resulted in an early increase in pulmonary T cell infiltrates following challenge with C. gattii. Overall, our studies show that C. gattii CW and CP protein preparations contain antigens that may be included in a subunit vaccine to induce prolonged protection against pulmonary C. gattii infection. Public Library of Science 2014-08-13 /pmc/articles/PMC4132117/ /pubmed/25119981 http://dx.doi.org/10.1371/journal.pone.0104316 Text en © 2014 Chaturvedi 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 Chaturvedi, Ashok K. Hameed, Rumanasma S. Wozniak, Karen L. Hole, Camaron R. Leopold Wager, Chrissy M. Weintraub, Susan T. Lopez-Ribot, Jose L. Wormley, Floyd L. Vaccine-Mediated Immune Responses to Experimental Pulmonary Cryptococcus gattii Infection in Mice |
title | Vaccine-Mediated Immune Responses to Experimental Pulmonary Cryptococcus gattii Infection in Mice |
title_full | Vaccine-Mediated Immune Responses to Experimental Pulmonary Cryptococcus gattii Infection in Mice |
title_fullStr | Vaccine-Mediated Immune Responses to Experimental Pulmonary Cryptococcus gattii Infection in Mice |
title_full_unstemmed | Vaccine-Mediated Immune Responses to Experimental Pulmonary Cryptococcus gattii Infection in Mice |
title_short | Vaccine-Mediated Immune Responses to Experimental Pulmonary Cryptococcus gattii Infection in Mice |
title_sort | vaccine-mediated immune responses to experimental pulmonary cryptococcus gattii infection in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132117/ https://www.ncbi.nlm.nih.gov/pubmed/25119981 http://dx.doi.org/10.1371/journal.pone.0104316 |
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