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Development of a Highly Protective Combination Monoclonal Antibody Therapy against Chikungunya Virus
Chikungunya virus (CHIKV) is a mosquito-transmitted alphavirus that causes global epidemics of a debilitating polyarthritis in humans. As there is a pressing need for the development of therapeutic agents, we screened 230 new mouse anti-CHIKV monoclonal antibodies (MAbs) for their ability to inhibit...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630103/ https://www.ncbi.nlm.nih.gov/pubmed/23637602 http://dx.doi.org/10.1371/journal.ppat.1003312 |
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author | Pal, Pankaj Dowd, Kimberly A. Brien, James D. Edeling, Melissa A. Gorlatov, Sergey Johnson, Syd Lee, Iris Akahata, Wataru Nabel, Gary J. Richter, Mareike K. S. Smit, Jolanda M. Fremont, Daved H. Pierson, Theodore C. Heise, Mark T. Diamond, Michael S. |
author_facet | Pal, Pankaj Dowd, Kimberly A. Brien, James D. Edeling, Melissa A. Gorlatov, Sergey Johnson, Syd Lee, Iris Akahata, Wataru Nabel, Gary J. Richter, Mareike K. S. Smit, Jolanda M. Fremont, Daved H. Pierson, Theodore C. Heise, Mark T. Diamond, Michael S. |
author_sort | Pal, Pankaj |
collection | PubMed |
description | Chikungunya virus (CHIKV) is a mosquito-transmitted alphavirus that causes global epidemics of a debilitating polyarthritis in humans. As there is a pressing need for the development of therapeutic agents, we screened 230 new mouse anti-CHIKV monoclonal antibodies (MAbs) for their ability to inhibit infection of all three CHIKV genotypes. Four of 36 neutralizing MAbs (CHK-102, CHK-152, CHK-166, and CHK-263) provided complete protection against lethality as prophylaxis in highly susceptible immunocompromised mice lacking the type I IFN receptor (Ifnar(−/−)) and mapped to distinct epitopes on the E1 and E2 structural proteins. CHK-152, the most protective MAb, was humanized, shown to block viral fusion, and require Fc effector function for optimal activity in vivo. In post-exposure therapeutic trials, administration of a single dose of a combination of two neutralizing MAbs (CHK-102+CHK-152 or CHK-166+CHK-152) limited the development of resistance and protected immunocompromised mice against disease when given 24 to 36 hours before CHIKV-induced death. Selected pairs of highly neutralizing MAbs may be a promising treatment option for CHIKV in humans. |
format | Online Article Text |
id | pubmed-3630103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36301032013-05-01 Development of a Highly Protective Combination Monoclonal Antibody Therapy against Chikungunya Virus Pal, Pankaj Dowd, Kimberly A. Brien, James D. Edeling, Melissa A. Gorlatov, Sergey Johnson, Syd Lee, Iris Akahata, Wataru Nabel, Gary J. Richter, Mareike K. S. Smit, Jolanda M. Fremont, Daved H. Pierson, Theodore C. Heise, Mark T. Diamond, Michael S. PLoS Pathog Research Article Chikungunya virus (CHIKV) is a mosquito-transmitted alphavirus that causes global epidemics of a debilitating polyarthritis in humans. As there is a pressing need for the development of therapeutic agents, we screened 230 new mouse anti-CHIKV monoclonal antibodies (MAbs) for their ability to inhibit infection of all three CHIKV genotypes. Four of 36 neutralizing MAbs (CHK-102, CHK-152, CHK-166, and CHK-263) provided complete protection against lethality as prophylaxis in highly susceptible immunocompromised mice lacking the type I IFN receptor (Ifnar(−/−)) and mapped to distinct epitopes on the E1 and E2 structural proteins. CHK-152, the most protective MAb, was humanized, shown to block viral fusion, and require Fc effector function for optimal activity in vivo. In post-exposure therapeutic trials, administration of a single dose of a combination of two neutralizing MAbs (CHK-102+CHK-152 or CHK-166+CHK-152) limited the development of resistance and protected immunocompromised mice against disease when given 24 to 36 hours before CHIKV-induced death. Selected pairs of highly neutralizing MAbs may be a promising treatment option for CHIKV in humans. Public Library of Science 2013-04-18 /pmc/articles/PMC3630103/ /pubmed/23637602 http://dx.doi.org/10.1371/journal.ppat.1003312 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Pal, Pankaj Dowd, Kimberly A. Brien, James D. Edeling, Melissa A. Gorlatov, Sergey Johnson, Syd Lee, Iris Akahata, Wataru Nabel, Gary J. Richter, Mareike K. S. Smit, Jolanda M. Fremont, Daved H. Pierson, Theodore C. Heise, Mark T. Diamond, Michael S. Development of a Highly Protective Combination Monoclonal Antibody Therapy against Chikungunya Virus |
title | Development of a Highly Protective Combination Monoclonal Antibody Therapy against Chikungunya Virus |
title_full | Development of a Highly Protective Combination Monoclonal Antibody Therapy against Chikungunya Virus |
title_fullStr | Development of a Highly Protective Combination Monoclonal Antibody Therapy against Chikungunya Virus |
title_full_unstemmed | Development of a Highly Protective Combination Monoclonal Antibody Therapy against Chikungunya Virus |
title_short | Development of a Highly Protective Combination Monoclonal Antibody Therapy against Chikungunya Virus |
title_sort | development of a highly protective combination monoclonal antibody therapy against chikungunya virus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630103/ https://www.ncbi.nlm.nih.gov/pubmed/23637602 http://dx.doi.org/10.1371/journal.ppat.1003312 |
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