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Development of a novel monoclonal antibody with reactivity to a wide range of Venezuelan equine encephalitis virus strains
BACKGROUND: There is currently a requirement for antiviral therapies capable of protecting against infection with Venezuelan equine encephalitis virus (VEEV), as a licensed vaccine is not available for general human use. Monoclonal antibodies are increasingly being developed as therapeutics and are...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2783036/ https://www.ncbi.nlm.nih.gov/pubmed/19925641 http://dx.doi.org/10.1186/1743-422X-6-206 |
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author | O'Brien, Lyn M Underwood-Fowler, Cindy D Goodchild, Sarah A Phelps, Amanda L Phillpotts, Robert J |
author_facet | O'Brien, Lyn M Underwood-Fowler, Cindy D Goodchild, Sarah A Phelps, Amanda L Phillpotts, Robert J |
author_sort | O'Brien, Lyn M |
collection | PubMed |
description | BACKGROUND: There is currently a requirement for antiviral therapies capable of protecting against infection with Venezuelan equine encephalitis virus (VEEV), as a licensed vaccine is not available for general human use. Monoclonal antibodies are increasingly being developed as therapeutics and are potential treatments for VEEV as they have been shown to be protective in the mouse model of disease. However, to be truly effective, the antibody should recognise multiple strains of VEEV and broadly reactive monoclonal antibodies are rarely and only coincidentally isolated using classical hybridoma technology. RESULTS: In this work, methods were developed to reliably derive broadly reactive murine antibodies. A phage library was created that expressed single chain variable fragments (scFv) isolated from mice immunised with multiple strains of VEEV. A broadly reactive scFv was identified and incorporated into a murine IgG2a framework. This novel antibody retained the broad reactivity exhibited by the scFv but did not possess virus neutralising activity. However, the antibody was still able to protect mice against VEEV disease induced by strain TrD when administered 24 h prior to challenge. CONCLUSION: A monoclonal antibody possessing reactivity to a wide range of VEEV strains may be of benefit as a generic antiviral therapy. However, humanisation of the murine antibody will be required before it can be tested in humans. Crown Copyright © 2009 |
format | Text |
id | pubmed-2783036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27830362009-11-26 Development of a novel monoclonal antibody with reactivity to a wide range of Venezuelan equine encephalitis virus strains O'Brien, Lyn M Underwood-Fowler, Cindy D Goodchild, Sarah A Phelps, Amanda L Phillpotts, Robert J Virol J Research BACKGROUND: There is currently a requirement for antiviral therapies capable of protecting against infection with Venezuelan equine encephalitis virus (VEEV), as a licensed vaccine is not available for general human use. Monoclonal antibodies are increasingly being developed as therapeutics and are potential treatments for VEEV as they have been shown to be protective in the mouse model of disease. However, to be truly effective, the antibody should recognise multiple strains of VEEV and broadly reactive monoclonal antibodies are rarely and only coincidentally isolated using classical hybridoma technology. RESULTS: In this work, methods were developed to reliably derive broadly reactive murine antibodies. A phage library was created that expressed single chain variable fragments (scFv) isolated from mice immunised with multiple strains of VEEV. A broadly reactive scFv was identified and incorporated into a murine IgG2a framework. This novel antibody retained the broad reactivity exhibited by the scFv but did not possess virus neutralising activity. However, the antibody was still able to protect mice against VEEV disease induced by strain TrD when administered 24 h prior to challenge. CONCLUSION: A monoclonal antibody possessing reactivity to a wide range of VEEV strains may be of benefit as a generic antiviral therapy. However, humanisation of the murine antibody will be required before it can be tested in humans. Crown Copyright © 2009 BioMed Central 2009-11-19 /pmc/articles/PMC2783036/ /pubmed/19925641 http://dx.doi.org/10.1186/1743-422X-6-206 Text en Copyright ©2009 O'Brien et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research O'Brien, Lyn M Underwood-Fowler, Cindy D Goodchild, Sarah A Phelps, Amanda L Phillpotts, Robert J Development of a novel monoclonal antibody with reactivity to a wide range of Venezuelan equine encephalitis virus strains |
title | Development of a novel monoclonal antibody with reactivity to a wide range of Venezuelan equine encephalitis virus strains |
title_full | Development of a novel monoclonal antibody with reactivity to a wide range of Venezuelan equine encephalitis virus strains |
title_fullStr | Development of a novel monoclonal antibody with reactivity to a wide range of Venezuelan equine encephalitis virus strains |
title_full_unstemmed | Development of a novel monoclonal antibody with reactivity to a wide range of Venezuelan equine encephalitis virus strains |
title_short | Development of a novel monoclonal antibody with reactivity to a wide range of Venezuelan equine encephalitis virus strains |
title_sort | development of a novel monoclonal antibody with reactivity to a wide range of venezuelan equine encephalitis virus strains |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2783036/ https://www.ncbi.nlm.nih.gov/pubmed/19925641 http://dx.doi.org/10.1186/1743-422X-6-206 |
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