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A new humanized antibody is effective against pathogenic fungi in vitro

Invasive fungal infections mainly affect patients undergoing transplantation, surgery, neoplastic disease, immunocompromised subjects and premature infants, and cause over 1.5 million deaths every year. The most common fungi isolated in invasive diseases are Candida spp., Cryptococcus spp., and Aspe...

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Autores principales: Di Mambro, Tomas, Vanzolini, Tania, Bruscolini, Pierpaolo, Perez-Gaviro, Sergio, Marra, Emanuele, Roscilli, Giuseppe, Bianchi, Marzia, Fraternale, Alessandra, Schiavano, Giuditta Fiorella, Canonico, Barbara, Magnani, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484667/
https://www.ncbi.nlm.nih.gov/pubmed/34593880
http://dx.doi.org/10.1038/s41598-021-98659-5
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author Di Mambro, Tomas
Vanzolini, Tania
Bruscolini, Pierpaolo
Perez-Gaviro, Sergio
Marra, Emanuele
Roscilli, Giuseppe
Bianchi, Marzia
Fraternale, Alessandra
Schiavano, Giuditta Fiorella
Canonico, Barbara
Magnani, Mauro
author_facet Di Mambro, Tomas
Vanzolini, Tania
Bruscolini, Pierpaolo
Perez-Gaviro, Sergio
Marra, Emanuele
Roscilli, Giuseppe
Bianchi, Marzia
Fraternale, Alessandra
Schiavano, Giuditta Fiorella
Canonico, Barbara
Magnani, Mauro
author_sort Di Mambro, Tomas
collection PubMed
description Invasive fungal infections mainly affect patients undergoing transplantation, surgery, neoplastic disease, immunocompromised subjects and premature infants, and cause over 1.5 million deaths every year. The most common fungi isolated in invasive diseases are Candida spp., Cryptococcus spp., and Aspergillus spp. and even if four classes of antifungals are available (Azoles, Echinocandins, Polyenes and Pyrimidine analogues), the side effects of drugs and fungal acquired and innate resistance represent the major hurdles to be overcome. Monoclonal antibodies are powerful tools currently used as diagnostic and therapeutic agents in different clinical contexts but not yet developed for the treatment of invasive fungal infections. In this paper we report the development of the first humanized monoclonal antibody specific for β-1,3 glucans, a vital component of several pathogenic fungi. H5K1 has been tested on C. auris, one of the most urgent threats and resulted efficient both alone and in combination with Caspofungin and Amphotericin B showing an enhancement effect. Our results support further preclinical and clinical developments for the use of H5K1 in the treatment of patients in need.
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spelling pubmed-84846672021-10-04 A new humanized antibody is effective against pathogenic fungi in vitro Di Mambro, Tomas Vanzolini, Tania Bruscolini, Pierpaolo Perez-Gaviro, Sergio Marra, Emanuele Roscilli, Giuseppe Bianchi, Marzia Fraternale, Alessandra Schiavano, Giuditta Fiorella Canonico, Barbara Magnani, Mauro Sci Rep Article Invasive fungal infections mainly affect patients undergoing transplantation, surgery, neoplastic disease, immunocompromised subjects and premature infants, and cause over 1.5 million deaths every year. The most common fungi isolated in invasive diseases are Candida spp., Cryptococcus spp., and Aspergillus spp. and even if four classes of antifungals are available (Azoles, Echinocandins, Polyenes and Pyrimidine analogues), the side effects of drugs and fungal acquired and innate resistance represent the major hurdles to be overcome. Monoclonal antibodies are powerful tools currently used as diagnostic and therapeutic agents in different clinical contexts but not yet developed for the treatment of invasive fungal infections. In this paper we report the development of the first humanized monoclonal antibody specific for β-1,3 glucans, a vital component of several pathogenic fungi. H5K1 has been tested on C. auris, one of the most urgent threats and resulted efficient both alone and in combination with Caspofungin and Amphotericin B showing an enhancement effect. Our results support further preclinical and clinical developments for the use of H5K1 in the treatment of patients in need. Nature Publishing Group UK 2021-09-30 /pmc/articles/PMC8484667/ /pubmed/34593880 http://dx.doi.org/10.1038/s41598-021-98659-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Di Mambro, Tomas
Vanzolini, Tania
Bruscolini, Pierpaolo
Perez-Gaviro, Sergio
Marra, Emanuele
Roscilli, Giuseppe
Bianchi, Marzia
Fraternale, Alessandra
Schiavano, Giuditta Fiorella
Canonico, Barbara
Magnani, Mauro
A new humanized antibody is effective against pathogenic fungi in vitro
title A new humanized antibody is effective against pathogenic fungi in vitro
title_full A new humanized antibody is effective against pathogenic fungi in vitro
title_fullStr A new humanized antibody is effective against pathogenic fungi in vitro
title_full_unstemmed A new humanized antibody is effective against pathogenic fungi in vitro
title_short A new humanized antibody is effective against pathogenic fungi in vitro
title_sort new humanized antibody is effective against pathogenic fungi in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484667/
https://www.ncbi.nlm.nih.gov/pubmed/34593880
http://dx.doi.org/10.1038/s41598-021-98659-5
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