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Development of a humanized monoclonal antibody with therapeutic potential against West Nile virus
Neutralization of West Nile virus (WNV) in vivo correlates with the development of an antibody response against the viral envelope (E) protein. Using random mutagenesis and yeast surface display, we defined individual contact residues of 14 newly generated monoclonal antibodies against domain III of...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group US
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1458527/ https://www.ncbi.nlm.nih.gov/pubmed/15852016 http://dx.doi.org/10.1038/nm1240 |
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author | Oliphant, Theodore Engle, Michael Nybakken, Grant E Doane, Chris Johnson, Syd Huang, Ling Gorlatov, Sergey Mehlhop, Erin Marri, Anantha Chung, Kyung Min Ebel, Gregory D Kramer, Laura D Fremont, Daved H Diamond, Michael S |
author_facet | Oliphant, Theodore Engle, Michael Nybakken, Grant E Doane, Chris Johnson, Syd Huang, Ling Gorlatov, Sergey Mehlhop, Erin Marri, Anantha Chung, Kyung Min Ebel, Gregory D Kramer, Laura D Fremont, Daved H Diamond, Michael S |
author_sort | Oliphant, Theodore |
collection | PubMed |
description | Neutralization of West Nile virus (WNV) in vivo correlates with the development of an antibody response against the viral envelope (E) protein. Using random mutagenesis and yeast surface display, we defined individual contact residues of 14 newly generated monoclonal antibodies against domain III of the WNV E protein. Monoclonal antibodies that strongly neutralized WNV localized to a surface patch on the lateral face of domain III. Convalescent antibodies from individuals who had recovered from WNV infection also detected this epitope. One monoclonal antibody, E16, neutralized 10 different strains in vitro, and showed therapeutic efficacy in mice, even when administered as a single dose 5 d after infection. A humanized version of E16 was generated that retained antigen specificity, avidity and neutralizing activity. In postexposure therapeutic trials in mice, a single dose of humanized E16 protected mice against WNV-induced mortality, and may therefore be a viable treatment option against WNV infection in humans. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nm1240) contains supplementary material, which is available to authorized users. |
format | Text |
id | pubmed-1458527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-14585272006-05-09 Development of a humanized monoclonal antibody with therapeutic potential against West Nile virus Oliphant, Theodore Engle, Michael Nybakken, Grant E Doane, Chris Johnson, Syd Huang, Ling Gorlatov, Sergey Mehlhop, Erin Marri, Anantha Chung, Kyung Min Ebel, Gregory D Kramer, Laura D Fremont, Daved H Diamond, Michael S Nat Med Article Neutralization of West Nile virus (WNV) in vivo correlates with the development of an antibody response against the viral envelope (E) protein. Using random mutagenesis and yeast surface display, we defined individual contact residues of 14 newly generated monoclonal antibodies against domain III of the WNV E protein. Monoclonal antibodies that strongly neutralized WNV localized to a surface patch on the lateral face of domain III. Convalescent antibodies from individuals who had recovered from WNV infection also detected this epitope. One monoclonal antibody, E16, neutralized 10 different strains in vitro, and showed therapeutic efficacy in mice, even when administered as a single dose 5 d after infection. A humanized version of E16 was generated that retained antigen specificity, avidity and neutralizing activity. In postexposure therapeutic trials in mice, a single dose of humanized E16 protected mice against WNV-induced mortality, and may therefore be a viable treatment option against WNV infection in humans. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nm1240) contains supplementary material, which is available to authorized users. Nature Publishing Group US 2005-04-24 2005 /pmc/articles/PMC1458527/ /pubmed/15852016 http://dx.doi.org/10.1038/nm1240 Text en © Nature Publishing Group 2005 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 Oliphant, Theodore Engle, Michael Nybakken, Grant E Doane, Chris Johnson, Syd Huang, Ling Gorlatov, Sergey Mehlhop, Erin Marri, Anantha Chung, Kyung Min Ebel, Gregory D Kramer, Laura D Fremont, Daved H Diamond, Michael S Development of a humanized monoclonal antibody with therapeutic potential against West Nile virus |
title | Development of a humanized monoclonal antibody with therapeutic potential against West Nile virus |
title_full | Development of a humanized monoclonal antibody with therapeutic potential against West Nile virus |
title_fullStr | Development of a humanized monoclonal antibody with therapeutic potential against West Nile virus |
title_full_unstemmed | Development of a humanized monoclonal antibody with therapeutic potential against West Nile virus |
title_short | Development of a humanized monoclonal antibody with therapeutic potential against West Nile virus |
title_sort | development of a humanized monoclonal antibody with therapeutic potential against west nile virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1458527/ https://www.ncbi.nlm.nih.gov/pubmed/15852016 http://dx.doi.org/10.1038/nm1240 |
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