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Drugs used for the treatment of cerebral and disseminated infections caused by free‐living amoebae

Free‐living amoebae (FLAs) are protozoa developing autonomously in diverse natural or artificial environments. The FLAs Acanthamoeba spp., Balamuthia mandrillaris, and Naegleria fowleri represent a risk for human health as they can become pathogenic and cause severe cerebral infections, named granul...

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Autores principales: Taravaud, Alexandre, Fechtali‐Moute, Zineb, Loiseau, Philippe M., Pomel, Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8212752/
https://www.ncbi.nlm.nih.gov/pubmed/33650319
http://dx.doi.org/10.1111/cts.12955
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author Taravaud, Alexandre
Fechtali‐Moute, Zineb
Loiseau, Philippe M.
Pomel, Sébastien
author_facet Taravaud, Alexandre
Fechtali‐Moute, Zineb
Loiseau, Philippe M.
Pomel, Sébastien
author_sort Taravaud, Alexandre
collection PubMed
description Free‐living amoebae (FLAs) are protozoa developing autonomously in diverse natural or artificial environments. The FLAs Acanthamoeba spp., Balamuthia mandrillaris, and Naegleria fowleri represent a risk for human health as they can become pathogenic and cause severe cerebral infections, named granulomatous amoebic encephalitis (GAE), Balamuthia amoebic encephalitis (BAE), and primary amoebic meningoencephalitis (PAM), respectively. Additionally, Acanthamoeba sp. can also rarely disseminate to diverse organs, such as the skin, sinuses, or bones, and cause extracerebral disseminated acanthamebiasis (EDA). No consensus treatment has been established for cerebral FLA infections or EDA. The therapy of cerebral and disseminated FLA infections often empirically associates a large diversity of drugs, all exhibiting a high toxicity. Nevertheless, these pathologies lead to a high mortality, above 90% of the cases, even in the presence of a treatment. In the present work, a total of 474 clinical cases of FLA infections gathered from the literature allowed to determine the frequency of usage, as well as the efficacy of the main drugs and drug combinations used in the treatment of these pathologies. The efficacy of drug usage was determined based on the survival rate after drug administration. The most efficient drugs, drug combinations, and their mechanism of action were discussed in regard to the present recommendations for the treatment of GAE, EDA, BAE, and PAM. At the end, this review aims to provide a useful tool for physicians in their choice to optimize the treatment of FLA infections.
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spelling pubmed-82127522021-06-25 Drugs used for the treatment of cerebral and disseminated infections caused by free‐living amoebae Taravaud, Alexandre Fechtali‐Moute, Zineb Loiseau, Philippe M. Pomel, Sébastien Clin Transl Sci Reviews Free‐living amoebae (FLAs) are protozoa developing autonomously in diverse natural or artificial environments. The FLAs Acanthamoeba spp., Balamuthia mandrillaris, and Naegleria fowleri represent a risk for human health as they can become pathogenic and cause severe cerebral infections, named granulomatous amoebic encephalitis (GAE), Balamuthia amoebic encephalitis (BAE), and primary amoebic meningoencephalitis (PAM), respectively. Additionally, Acanthamoeba sp. can also rarely disseminate to diverse organs, such as the skin, sinuses, or bones, and cause extracerebral disseminated acanthamebiasis (EDA). No consensus treatment has been established for cerebral FLA infections or EDA. The therapy of cerebral and disseminated FLA infections often empirically associates a large diversity of drugs, all exhibiting a high toxicity. Nevertheless, these pathologies lead to a high mortality, above 90% of the cases, even in the presence of a treatment. In the present work, a total of 474 clinical cases of FLA infections gathered from the literature allowed to determine the frequency of usage, as well as the efficacy of the main drugs and drug combinations used in the treatment of these pathologies. The efficacy of drug usage was determined based on the survival rate after drug administration. The most efficient drugs, drug combinations, and their mechanism of action were discussed in regard to the present recommendations for the treatment of GAE, EDA, BAE, and PAM. At the end, this review aims to provide a useful tool for physicians in their choice to optimize the treatment of FLA infections. John Wiley and Sons Inc. 2021-03-01 2021-05 /pmc/articles/PMC8212752/ /pubmed/33650319 http://dx.doi.org/10.1111/cts.12955 Text en © 2021 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of the American Society for Clinical Pharmacology and Therapeutics. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reviews
Taravaud, Alexandre
Fechtali‐Moute, Zineb
Loiseau, Philippe M.
Pomel, Sébastien
Drugs used for the treatment of cerebral and disseminated infections caused by free‐living amoebae
title Drugs used for the treatment of cerebral and disseminated infections caused by free‐living amoebae
title_full Drugs used for the treatment of cerebral and disseminated infections caused by free‐living amoebae
title_fullStr Drugs used for the treatment of cerebral and disseminated infections caused by free‐living amoebae
title_full_unstemmed Drugs used for the treatment of cerebral and disseminated infections caused by free‐living amoebae
title_short Drugs used for the treatment of cerebral and disseminated infections caused by free‐living amoebae
title_sort drugs used for the treatment of cerebral and disseminated infections caused by free‐living amoebae
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8212752/
https://www.ncbi.nlm.nih.gov/pubmed/33650319
http://dx.doi.org/10.1111/cts.12955
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