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Chickens with humanized immunoglobulin genes generate antibodies with high affinity and broad epitope coverage to conserved targets
Transgenic animal platforms for the discovery of human monoclonal antibodies have been developed in mice, rats, rabbits and cows. The immune response to human proteins is limited in these animals by their tolerance to mammalian-conserved epitopes. To expand the range of epitopes that are accessible,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800366/ https://www.ncbi.nlm.nih.gov/pubmed/29035625 http://dx.doi.org/10.1080/19420862.2017.1386825 |
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author | Ching, Kathryn H. Collarini, Ellen J. Abdiche, Yasmina N. Bedinger, Daniel Pedersen, Darlene Izquierdo, Shelley Harriman, Rian Zhu, Lei Etches, Robert J. van de Lavoir, Marie-Cecile Harriman, William D. Leighton, Philip A. |
author_facet | Ching, Kathryn H. Collarini, Ellen J. Abdiche, Yasmina N. Bedinger, Daniel Pedersen, Darlene Izquierdo, Shelley Harriman, Rian Zhu, Lei Etches, Robert J. van de Lavoir, Marie-Cecile Harriman, William D. Leighton, Philip A. |
author_sort | Ching, Kathryn H. |
collection | PubMed |
description | Transgenic animal platforms for the discovery of human monoclonal antibodies have been developed in mice, rats, rabbits and cows. The immune response to human proteins is limited in these animals by their tolerance to mammalian-conserved epitopes. To expand the range of epitopes that are accessible, we have chosen an animal host that is less phylogenetically related to humans. Specifically, we generated transgenic chickens expressing antibodies from immunoglobulin heavy and light chain loci containing human variable regions and chicken constant regions. From these birds, paired human light and heavy chain variable regions are recovered and cloned as fully human recombinant antibodies. The human antibody-expressing chickens exhibit normal B cell development and raise immune responses to conserved human proteins that are not immunogenic in mice. Fully human monoclonal antibodies can be recovered with sub-nanomolar affinities. Binning data of antibodies to a human protein show epitope coverage similar to wild type chickens, which we previously showed is broader than that produced from rodent immunizations. |
format | Online Article Text |
id | pubmed-5800366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-58003662018-02-12 Chickens with humanized immunoglobulin genes generate antibodies with high affinity and broad epitope coverage to conserved targets Ching, Kathryn H. Collarini, Ellen J. Abdiche, Yasmina N. Bedinger, Daniel Pedersen, Darlene Izquierdo, Shelley Harriman, Rian Zhu, Lei Etches, Robert J. van de Lavoir, Marie-Cecile Harriman, William D. Leighton, Philip A. MAbs Report Transgenic animal platforms for the discovery of human monoclonal antibodies have been developed in mice, rats, rabbits and cows. The immune response to human proteins is limited in these animals by their tolerance to mammalian-conserved epitopes. To expand the range of epitopes that are accessible, we have chosen an animal host that is less phylogenetically related to humans. Specifically, we generated transgenic chickens expressing antibodies from immunoglobulin heavy and light chain loci containing human variable regions and chicken constant regions. From these birds, paired human light and heavy chain variable regions are recovered and cloned as fully human recombinant antibodies. The human antibody-expressing chickens exhibit normal B cell development and raise immune responses to conserved human proteins that are not immunogenic in mice. Fully human monoclonal antibodies can be recovered with sub-nanomolar affinities. Binning data of antibodies to a human protein show epitope coverage similar to wild type chickens, which we previously showed is broader than that produced from rodent immunizations. Taylor & Francis 2017-11-02 /pmc/articles/PMC5800366/ /pubmed/29035625 http://dx.doi.org/10.1080/19420862.2017.1386825 Text en © 2018 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Report Ching, Kathryn H. Collarini, Ellen J. Abdiche, Yasmina N. Bedinger, Daniel Pedersen, Darlene Izquierdo, Shelley Harriman, Rian Zhu, Lei Etches, Robert J. van de Lavoir, Marie-Cecile Harriman, William D. Leighton, Philip A. Chickens with humanized immunoglobulin genes generate antibodies with high affinity and broad epitope coverage to conserved targets |
title | Chickens with humanized immunoglobulin genes generate antibodies with high affinity and broad epitope coverage to conserved targets |
title_full | Chickens with humanized immunoglobulin genes generate antibodies with high affinity and broad epitope coverage to conserved targets |
title_fullStr | Chickens with humanized immunoglobulin genes generate antibodies with high affinity and broad epitope coverage to conserved targets |
title_full_unstemmed | Chickens with humanized immunoglobulin genes generate antibodies with high affinity and broad epitope coverage to conserved targets |
title_short | Chickens with humanized immunoglobulin genes generate antibodies with high affinity and broad epitope coverage to conserved targets |
title_sort | chickens with humanized immunoglobulin genes generate antibodies with high affinity and broad epitope coverage to conserved targets |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800366/ https://www.ncbi.nlm.nih.gov/pubmed/29035625 http://dx.doi.org/10.1080/19420862.2017.1386825 |
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