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Antibody-based therapies for emerging infectious diseases.

In the 19th century, it was discovered that immune sera were useful in treating infectious diseases. Serum therapy was largely abandoned in the 1940s because of the toxicity associated with the administration of heterologous sera and the introduction of effective antimicrobial chemotherapy. Recent a...

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Autor principal: Casadevall, A
Formato: Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2626792/
https://www.ncbi.nlm.nih.gov/pubmed/8903230
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author Casadevall, A
author_facet Casadevall, A
author_sort Casadevall, A
collection PubMed
description In the 19th century, it was discovered that immune sera were useful in treating infectious diseases. Serum therapy was largely abandoned in the 1940s because of the toxicity associated with the administration of heterologous sera and the introduction of effective antimicrobial chemotherapy. Recent advances in the technology of monoclonal antibody production provide the means to generate human antibody reagents and reintroduce antibody therapies, while avoiding the toxicities associated with serum therapy. Because of the versatility of antibodies, antibody-based therapies could, in theory, be developed against any existing pathogen. The advantages of antibody-based therapies include versatility, low toxicity, pathogen specificity, enhancement of immune function, and favorable pharmacokinetics; the disadvantages include high cost, limited usefulness against mixed infections, and the need for early and precise microbiologic diagnosis. The potential of antibodies as antiinfective agents has not been fully tapped. Antibody-based therapies constitute a potentially useful option against newly emergent pathogens.
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spelling pubmed-26267922009-05-20 Antibody-based therapies for emerging infectious diseases. Casadevall, A Emerg Infect Dis Research Article In the 19th century, it was discovered that immune sera were useful in treating infectious diseases. Serum therapy was largely abandoned in the 1940s because of the toxicity associated with the administration of heterologous sera and the introduction of effective antimicrobial chemotherapy. Recent advances in the technology of monoclonal antibody production provide the means to generate human antibody reagents and reintroduce antibody therapies, while avoiding the toxicities associated with serum therapy. Because of the versatility of antibodies, antibody-based therapies could, in theory, be developed against any existing pathogen. The advantages of antibody-based therapies include versatility, low toxicity, pathogen specificity, enhancement of immune function, and favorable pharmacokinetics; the disadvantages include high cost, limited usefulness against mixed infections, and the need for early and precise microbiologic diagnosis. The potential of antibodies as antiinfective agents has not been fully tapped. Antibody-based therapies constitute a potentially useful option against newly emergent pathogens. Centers for Disease Control and Prevention 1996 /pmc/articles/PMC2626792/ /pubmed/8903230 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Research Article
Casadevall, A
Antibody-based therapies for emerging infectious diseases.
title Antibody-based therapies for emerging infectious diseases.
title_full Antibody-based therapies for emerging infectious diseases.
title_fullStr Antibody-based therapies for emerging infectious diseases.
title_full_unstemmed Antibody-based therapies for emerging infectious diseases.
title_short Antibody-based therapies for emerging infectious diseases.
title_sort antibody-based therapies for emerging infectious diseases.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2626792/
https://www.ncbi.nlm.nih.gov/pubmed/8903230
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