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Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases

Using a comprehensive set of discovery and optimization tools, antibodies were produced with the ability to neutralize SARS coronavirus (SARS-CoV) infection in Vero E6 cells and in animal models. These anti-SARS antibodies were discovered using a novel DNA display method, which can identify new anti...

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Autores principales: Rogers, J., Schoepp, R.J., Schröder, O., Clements, T.L., Holland, T.F., Li, J.Q., Li, J., Lewis, L.M., Dirmeier, R.P., Frey, G.J., Tan, X., Wong, K., Woodnutt, G., Keller, M., Reed, D.S., Kimmel, B.E., Tozer, E.C.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2461042/
https://www.ncbi.nlm.nih.gov/pubmed/18480090
http://dx.doi.org/10.1093/protein/gzn027
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author Rogers, J.
Schoepp, R.J.
Schröder, O.
Clements, T.L.
Holland, T.F.
Li, J.Q.
Li, J.
Lewis, L.M.
Dirmeier, R.P.
Frey, G.J.
Tan, X.
Wong, K.
Woodnutt, G.
Keller, M.
Reed, D.S.
Kimmel, B.E.
Tozer, E.C.
author_facet Rogers, J.
Schoepp, R.J.
Schröder, O.
Clements, T.L.
Holland, T.F.
Li, J.Q.
Li, J.
Lewis, L.M.
Dirmeier, R.P.
Frey, G.J.
Tan, X.
Wong, K.
Woodnutt, G.
Keller, M.
Reed, D.S.
Kimmel, B.E.
Tozer, E.C.
author_sort Rogers, J.
collection PubMed
description Using a comprehensive set of discovery and optimization tools, antibodies were produced with the ability to neutralize SARS coronavirus (SARS-CoV) infection in Vero E6 cells and in animal models. These anti-SARS antibodies were discovered using a novel DNA display method, which can identify new antibodies within days. Once neutralizing antibodies were identified, a comprehensive and effective means of converting the mouse sequences to human frameworks was accomplished using HuFR™ (human framework reassembly) technology. The best variant (61G4) from this screen showed a 3.5–4-fold improvement in neutralization of SARS-CoV infection in vitro. Finally, using a complete site-saturation mutagenesis methodology focused on the CDR (complementarity determining regions), a single point mutation (51E7) was identified that improved the 80% plaque reduction neutralization of the virus by greater than 8-fold. These discovery and evolution strategies can be applied to any emerging pathogen or toxin where a causative agent is known.
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spelling pubmed-24610422009-02-25 Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases Rogers, J. Schoepp, R.J. Schröder, O. Clements, T.L. Holland, T.F. Li, J.Q. Li, J. Lewis, L.M. Dirmeier, R.P. Frey, G.J. Tan, X. Wong, K. Woodnutt, G. Keller, M. Reed, D.S. Kimmel, B.E. Tozer, E.C. Protein Eng Des Sel Original Articles Using a comprehensive set of discovery and optimization tools, antibodies were produced with the ability to neutralize SARS coronavirus (SARS-CoV) infection in Vero E6 cells and in animal models. These anti-SARS antibodies were discovered using a novel DNA display method, which can identify new antibodies within days. Once neutralizing antibodies were identified, a comprehensive and effective means of converting the mouse sequences to human frameworks was accomplished using HuFR™ (human framework reassembly) technology. The best variant (61G4) from this screen showed a 3.5–4-fold improvement in neutralization of SARS-CoV infection in vitro. Finally, using a complete site-saturation mutagenesis methodology focused on the CDR (complementarity determining regions), a single point mutation (51E7) was identified that improved the 80% plaque reduction neutralization of the virus by greater than 8-fold. These discovery and evolution strategies can be applied to any emerging pathogen or toxin where a causative agent is known. Oxford University Press 2008-08 2008-05-13 /pmc/articles/PMC2461042/ /pubmed/18480090 http://dx.doi.org/10.1093/protein/gzn027 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Rogers, J.
Schoepp, R.J.
Schröder, O.
Clements, T.L.
Holland, T.F.
Li, J.Q.
Li, J.
Lewis, L.M.
Dirmeier, R.P.
Frey, G.J.
Tan, X.
Wong, K.
Woodnutt, G.
Keller, M.
Reed, D.S.
Kimmel, B.E.
Tozer, E.C.
Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases
title Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases
title_full Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases
title_fullStr Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases
title_full_unstemmed Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases
title_short Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases
title_sort rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2461042/
https://www.ncbi.nlm.nih.gov/pubmed/18480090
http://dx.doi.org/10.1093/protein/gzn027
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