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Exploring the Native Human Antibody Repertoire to Create Antiviral Therapeutics

Native human antibodies are defined as those that arise naturally as the result of the functioning of an intact human immune system. The utility of native antibodies for the treatment of human viral diseases has been established through experience with hyperimmune human globulins. Native antibodies,...

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Detalles Bibliográficos
Autores principales: Dessain, Scott K., Adekar, S. P., Berry, J. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121815/
https://www.ncbi.nlm.nih.gov/pubmed/17990793
http://dx.doi.org/10.1007/978-3-540-72146-8_6
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author Dessain, Scott K.
Adekar, S. P.
Berry, J. D.
author_facet Dessain, Scott K.
Adekar, S. P.
Berry, J. D.
author_sort Dessain, Scott K.
collection PubMed
description Native human antibodies are defined as those that arise naturally as the result of the functioning of an intact human immune system. The utility of native antibodies for the treatment of human viral diseases has been established through experience with hyperimmune human globulins. Native antibodies, as a class, differ in some respects from those obtained by recombinant library methods (phage or transgenic mouse) and possess distinct properties that may make them ideal therapeutics for human viral diseases. Methods for cloning native human antibodies have been beset by technical problems, yet many antibodies specific for viral antigens have been cloned. In the present review, we discuss native human antibodies and ongoing improvements in cloning methods that should facilitate the creation of novel, potent antiviral therapeutics obtained from the native human antibody repertoire.
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spelling pubmed-71218152020-04-06 Exploring the Native Human Antibody Repertoire to Create Antiviral Therapeutics Dessain, Scott K. Adekar, S. P. Berry, J. D. Human Antibody Therapeutics for Viral Disease Article Native human antibodies are defined as those that arise naturally as the result of the functioning of an intact human immune system. The utility of native antibodies for the treatment of human viral diseases has been established through experience with hyperimmune human globulins. Native antibodies, as a class, differ in some respects from those obtained by recombinant library methods (phage or transgenic mouse) and possess distinct properties that may make them ideal therapeutics for human viral diseases. Methods for cloning native human antibodies have been beset by technical problems, yet many antibodies specific for viral antigens have been cloned. In the present review, we discuss native human antibodies and ongoing improvements in cloning methods that should facilitate the creation of novel, potent antiviral therapeutics obtained from the native human antibody repertoire. 2008 /pmc/articles/PMC7121815/ /pubmed/17990793 http://dx.doi.org/10.1007/978-3-540-72146-8_6 Text en © Springer-Verlag Berlin Heidelberg 2008 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Dessain, Scott K.
Adekar, S. P.
Berry, J. D.
Exploring the Native Human Antibody Repertoire to Create Antiviral Therapeutics
title Exploring the Native Human Antibody Repertoire to Create Antiviral Therapeutics
title_full Exploring the Native Human Antibody Repertoire to Create Antiviral Therapeutics
title_fullStr Exploring the Native Human Antibody Repertoire to Create Antiviral Therapeutics
title_full_unstemmed Exploring the Native Human Antibody Repertoire to Create Antiviral Therapeutics
title_short Exploring the Native Human Antibody Repertoire to Create Antiviral Therapeutics
title_sort exploring the native human antibody repertoire to create antiviral therapeutics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121815/
https://www.ncbi.nlm.nih.gov/pubmed/17990793
http://dx.doi.org/10.1007/978-3-540-72146-8_6
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