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Development of a Mouse Monoclonal Antibody Cocktail for Post-exposure Rabies Prophylaxis in Humans

As the demand for rabies post-exposure prophylaxis (PEP) treatments has increased exponentially in recent years, the limited supply of human and equine rabies immunoglobulin (HRIG and ERIG) has failed to provide the required passive immune component in PEP in countries where canine rabies is endemic...

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Autores principales: Müller, Thomas, Dietzschold, Bernhard, Ertl, Hildegund, Fooks, Anthony R., Freuling, Conrad, Fehlner-Gardiner, Christine, Kliemt, Jeannette, Meslin, Francois X., Rupprecht, Charles E., Tordo, Noël, Wanderler, Alexander I., Kieny, Marie Paule
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765635/
https://www.ncbi.nlm.nih.gov/pubmed/19888334
http://dx.doi.org/10.1371/journal.pntd.0000542
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author Müller, Thomas
Dietzschold, Bernhard
Ertl, Hildegund
Fooks, Anthony R.
Freuling, Conrad
Fehlner-Gardiner, Christine
Kliemt, Jeannette
Meslin, Francois X.
Rupprecht, Charles E.
Tordo, Noël
Wanderler, Alexander I.
Kieny, Marie Paule
author_facet Müller, Thomas
Dietzschold, Bernhard
Ertl, Hildegund
Fooks, Anthony R.
Freuling, Conrad
Fehlner-Gardiner, Christine
Kliemt, Jeannette
Meslin, Francois X.
Rupprecht, Charles E.
Tordo, Noël
Wanderler, Alexander I.
Kieny, Marie Paule
author_sort Müller, Thomas
collection PubMed
description As the demand for rabies post-exposure prophylaxis (PEP) treatments has increased exponentially in recent years, the limited supply of human and equine rabies immunoglobulin (HRIG and ERIG) has failed to provide the required passive immune component in PEP in countries where canine rabies is endemic. Replacement of HRIG and ERIG with a potentially cheaper and efficacious alternative biological for treatment of rabies in humans, therefore, remains a high priority. In this study, we set out to assess a mouse monoclonal antibody (MoMAb) cocktail with the ultimate goal to develop a product at the lowest possible cost that can be used in developing countries as a replacement for RIG in PEP. Five MoMAbs, E559.9.14, 1112-1, 62-71-3, M727-5-1, and M777-16-3, were selected from available panels based on stringent criteria, such as biological activity, neutralizing potency, binding specificity, spectrum of neutralization of lyssaviruses, and history of each hybridoma. Four of these MoMAbs recognize epitopes in antigenic site II and one recognizes an epitope in antigenic site III on the rabies virus (RABV) glycoprotein, as determined by nucleotide sequence analysis of the glycoprotein gene of unique MoMAb neutralization-escape mutants. The MoMAbs were produced under Good Laboratory Practice (GLP) conditions. Unique combinations (cocktails) were prepared, using different concentrations of the MoMAbs that were capable of targeting non-overlapping epitopes of antigenic sites II and III. Blind in vitro efficacy studies showed the MoMab cocktails neutralized a broad spectrum of lyssaviruses except for lyssaviruses belonging to phylogroups II and III. In vivo, MoMAb cocktails resulted in protection as a component of PEP that was comparable to HRIG. In conclusion, all three novel combinations of MoMAbs were shown to have equal efficacy to HRIG and therefore could be considered a potentially less expensive alternative biological agent for use in PEP and prevention of rabies in humans.
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spelling pubmed-27656352009-11-04 Development of a Mouse Monoclonal Antibody Cocktail for Post-exposure Rabies Prophylaxis in Humans Müller, Thomas Dietzschold, Bernhard Ertl, Hildegund Fooks, Anthony R. Freuling, Conrad Fehlner-Gardiner, Christine Kliemt, Jeannette Meslin, Francois X. Rupprecht, Charles E. Tordo, Noël Wanderler, Alexander I. Kieny, Marie Paule PLoS Negl Trop Dis Research Article As the demand for rabies post-exposure prophylaxis (PEP) treatments has increased exponentially in recent years, the limited supply of human and equine rabies immunoglobulin (HRIG and ERIG) has failed to provide the required passive immune component in PEP in countries where canine rabies is endemic. Replacement of HRIG and ERIG with a potentially cheaper and efficacious alternative biological for treatment of rabies in humans, therefore, remains a high priority. In this study, we set out to assess a mouse monoclonal antibody (MoMAb) cocktail with the ultimate goal to develop a product at the lowest possible cost that can be used in developing countries as a replacement for RIG in PEP. Five MoMAbs, E559.9.14, 1112-1, 62-71-3, M727-5-1, and M777-16-3, were selected from available panels based on stringent criteria, such as biological activity, neutralizing potency, binding specificity, spectrum of neutralization of lyssaviruses, and history of each hybridoma. Four of these MoMAbs recognize epitopes in antigenic site II and one recognizes an epitope in antigenic site III on the rabies virus (RABV) glycoprotein, as determined by nucleotide sequence analysis of the glycoprotein gene of unique MoMAb neutralization-escape mutants. The MoMAbs were produced under Good Laboratory Practice (GLP) conditions. Unique combinations (cocktails) were prepared, using different concentrations of the MoMAbs that were capable of targeting non-overlapping epitopes of antigenic sites II and III. Blind in vitro efficacy studies showed the MoMab cocktails neutralized a broad spectrum of lyssaviruses except for lyssaviruses belonging to phylogroups II and III. In vivo, MoMAb cocktails resulted in protection as a component of PEP that was comparable to HRIG. In conclusion, all three novel combinations of MoMAbs were shown to have equal efficacy to HRIG and therefore could be considered a potentially less expensive alternative biological agent for use in PEP and prevention of rabies in humans. Public Library of Science 2009-11-03 /pmc/articles/PMC2765635/ /pubmed/19888334 http://dx.doi.org/10.1371/journal.pntd.0000542 Text en 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. 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
Müller, Thomas
Dietzschold, Bernhard
Ertl, Hildegund
Fooks, Anthony R.
Freuling, Conrad
Fehlner-Gardiner, Christine
Kliemt, Jeannette
Meslin, Francois X.
Rupprecht, Charles E.
Tordo, Noël
Wanderler, Alexander I.
Kieny, Marie Paule
Development of a Mouse Monoclonal Antibody Cocktail for Post-exposure Rabies Prophylaxis in Humans
title Development of a Mouse Monoclonal Antibody Cocktail for Post-exposure Rabies Prophylaxis in Humans
title_full Development of a Mouse Monoclonal Antibody Cocktail for Post-exposure Rabies Prophylaxis in Humans
title_fullStr Development of a Mouse Monoclonal Antibody Cocktail for Post-exposure Rabies Prophylaxis in Humans
title_full_unstemmed Development of a Mouse Monoclonal Antibody Cocktail for Post-exposure Rabies Prophylaxis in Humans
title_short Development of a Mouse Monoclonal Antibody Cocktail for Post-exposure Rabies Prophylaxis in Humans
title_sort development of a mouse monoclonal antibody cocktail for post-exposure rabies prophylaxis in humans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765635/
https://www.ncbi.nlm.nih.gov/pubmed/19888334
http://dx.doi.org/10.1371/journal.pntd.0000542
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