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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
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.
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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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