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Anti-CotH3 antibodies protect mice from mucormycosis by prevention of invasion and augmenting opsonophagocytosis
Mucorales are fungal pathogens that cause mucormycosis, a lethal angioinvasive disease. Previously, we demonstrated that Rhizopus, the most common cause of mucormycosis, invades endothelial cells by binding of its CotH proteins to the host receptor GRP78. Loss of CotH3 renders the fungus noninvasive...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561750/ https://www.ncbi.nlm.nih.gov/pubmed/31206021 http://dx.doi.org/10.1126/sciadv.aaw1327 |
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author | Gebremariam, Teclegiorgis Alkhazraji, Sondus Soliman, Sameh S. M. Gu, Yiyou Jeon, Heewon H. Zhang, Lina French, Samuel W. Stevens, David A. Edwards, John E. Filler, Scott G. Uppuluri, Priya Ibrahim, Ashraf S. |
author_facet | Gebremariam, Teclegiorgis Alkhazraji, Sondus Soliman, Sameh S. M. Gu, Yiyou Jeon, Heewon H. Zhang, Lina French, Samuel W. Stevens, David A. Edwards, John E. Filler, Scott G. Uppuluri, Priya Ibrahim, Ashraf S. |
author_sort | Gebremariam, Teclegiorgis |
collection | PubMed |
description | Mucorales are fungal pathogens that cause mucormycosis, a lethal angioinvasive disease. Previously, we demonstrated that Rhizopus, the most common cause of mucormycosis, invades endothelial cells by binding of its CotH proteins to the host receptor GRP78. Loss of CotH3 renders the fungus noninvasive and attenuates Rhizopus virulence in mice. Here, we demonstrate that polyclonal antibodies raised against peptides of CotH3 protected diabetic ketoacidotic (DKA) and neutropenic mice from mucormycosis compared to mice treated with control preimmune serum. Passive immunization with anti-CotH3 antibodies enhanced neutrophil inlfux and triggered Fc receptor-mediated enhanced opsonophagocytosis killing of Rhizopus delemar. Monoclonal antibodies raised against the CotH3 peptide also protected immunosuppressed mice from mucormycosis caused by R. delemar and other Mucorales and acted synergistically with antifungal drugs in protecting DKA mice from R. delemar infection. These data identify anti-CotH3 antibodies as a promising adjunctive immunotherapeutic option against a deadly disease that often poses a therapeutic challenge. |
format | Online Article Text |
id | pubmed-6561750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-65617502019-06-14 Anti-CotH3 antibodies protect mice from mucormycosis by prevention of invasion and augmenting opsonophagocytosis Gebremariam, Teclegiorgis Alkhazraji, Sondus Soliman, Sameh S. M. Gu, Yiyou Jeon, Heewon H. Zhang, Lina French, Samuel W. Stevens, David A. Edwards, John E. Filler, Scott G. Uppuluri, Priya Ibrahim, Ashraf S. Sci Adv Research Articles Mucorales are fungal pathogens that cause mucormycosis, a lethal angioinvasive disease. Previously, we demonstrated that Rhizopus, the most common cause of mucormycosis, invades endothelial cells by binding of its CotH proteins to the host receptor GRP78. Loss of CotH3 renders the fungus noninvasive and attenuates Rhizopus virulence in mice. Here, we demonstrate that polyclonal antibodies raised against peptides of CotH3 protected diabetic ketoacidotic (DKA) and neutropenic mice from mucormycosis compared to mice treated with control preimmune serum. Passive immunization with anti-CotH3 antibodies enhanced neutrophil inlfux and triggered Fc receptor-mediated enhanced opsonophagocytosis killing of Rhizopus delemar. Monoclonal antibodies raised against the CotH3 peptide also protected immunosuppressed mice from mucormycosis caused by R. delemar and other Mucorales and acted synergistically with antifungal drugs in protecting DKA mice from R. delemar infection. These data identify anti-CotH3 antibodies as a promising adjunctive immunotherapeutic option against a deadly disease that often poses a therapeutic challenge. American Association for the Advancement of Science 2019-06-12 /pmc/articles/PMC6561750/ /pubmed/31206021 http://dx.doi.org/10.1126/sciadv.aaw1327 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Gebremariam, Teclegiorgis Alkhazraji, Sondus Soliman, Sameh S. M. Gu, Yiyou Jeon, Heewon H. Zhang, Lina French, Samuel W. Stevens, David A. Edwards, John E. Filler, Scott G. Uppuluri, Priya Ibrahim, Ashraf S. Anti-CotH3 antibodies protect mice from mucormycosis by prevention of invasion and augmenting opsonophagocytosis |
title | Anti-CotH3 antibodies protect mice from mucormycosis by prevention of invasion and augmenting opsonophagocytosis |
title_full | Anti-CotH3 antibodies protect mice from mucormycosis by prevention of invasion and augmenting opsonophagocytosis |
title_fullStr | Anti-CotH3 antibodies protect mice from mucormycosis by prevention of invasion and augmenting opsonophagocytosis |
title_full_unstemmed | Anti-CotH3 antibodies protect mice from mucormycosis by prevention of invasion and augmenting opsonophagocytosis |
title_short | Anti-CotH3 antibodies protect mice from mucormycosis by prevention of invasion and augmenting opsonophagocytosis |
title_sort | anti-coth3 antibodies protect mice from mucormycosis by prevention of invasion and augmenting opsonophagocytosis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561750/ https://www.ncbi.nlm.nih.gov/pubmed/31206021 http://dx.doi.org/10.1126/sciadv.aaw1327 |
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