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 , 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 att...

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Veröffentlicht in:Science advances 2019-06, Vol.5 (6), p.eaaw1327-eaaw1327
Hauptverfasser: Gebremariam, Teclegiorgis, Alkhazraji, Sondus, Soliman, Sameh S M, Gu, Yiyou, Jeon, Heewon H, Zhang, Lina, French, Samuel W, Stevens, David A, Edwards, Jr, John E, Filler, Scott G, Uppuluri, Priya, Ibrahim, Ashraf S
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container_title Science advances
container_volume 5
creator Gebremariam, Teclegiorgis
Alkhazraji, Sondus
Soliman, Sameh S M
Gu, Yiyou
Jeon, Heewon H
Zhang, Lina
French, Samuel W
Stevens, David A
Edwards, Jr, John E
Filler, Scott G
Uppuluri, Priya
Ibrahim, Ashraf S
description Mucorales are fungal pathogens that cause mucormycosis, a lethal angioinvasive disease. Previously, we demonstrated that , 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 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 . Monoclonal antibodies raised against the CotH3 peptide also protected immunosuppressed mice from mucormycosis caused by and other Mucorales and acted synergistically with antifungal drugs in protecting DKA mice from infection. These data identify anti-CotH3 antibodies as a promising adjunctive immunotherapeutic option against a deadly disease that often poses a therapeutic challenge.
doi_str_mv 10.1126/sciadv.aaw1327
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subjects Animals
Antibodies, Fungal - biosynthesis
Antibodies, Fungal - pharmacology
Antibodies, Monoclonal - biosynthesis
Antibodies, Monoclonal - pharmacology
Antifungal Agents - pharmacology
Combined Modality Therapy
Diabetic Ketoacidosis - immunology
Diabetic Ketoacidosis - microbiology
Diabetic Ketoacidosis - mortality
Diabetic Ketoacidosis - therapy
Disease Models, Animal
Fungal Proteins - genetics
Fungal Proteins - immunology
Gene Expression
Health and Medicine
Heat-Shock Proteins - genetics
Heat-Shock Proteins - immunology
Host-Pathogen Interactions - immunology
Humans
Immunization, Passive - methods
Immunocompromised Host
Male
Mice
Mice, Inbred ICR
Mucormycosis - immunology
Mucormycosis - microbiology
Mucormycosis - mortality
Mucormycosis - therapy
Neutropenia - immunology
Neutropenia - microbiology
Neutropenia - mortality
Neutropenia - therapy
Neutrophils - drug effects
Neutrophils - immunology
Neutrophils - microbiology
Phagocytosis - drug effects
Receptors, Immunologic - genetics
Receptors, Immunologic - immunology
Rhizopus - drug effects
Rhizopus - pathogenicity
SciAdv r-articles
Survival Analysis
Virulence
title Anti-CotH3 antibodies protect mice from mucormycosis by prevention of invasion and augmenting opsonophagocytosis
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