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Engineering monoclonal antibody-based contraception and multipurpose prevention technologies(†)

Sexually transmitted infections are highly prevalent, and over 40% of pregnancies are unplanned. We are producing new antibody-based multipurpose prevention technology products to address these problems and fill an unmet need in female reproductive health. We used a Nicotiana platform to manufacture...

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Autores principales: Anderson, Deborah J, Politch, Joseph A, Cone, Richard A, Zeitlin, Larry, Lai, Samuel K, Santangelo, Philip J, Moench, Thomas R, Whaley, Kevin J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401387/
https://www.ncbi.nlm.nih.gov/pubmed/32607584
http://dx.doi.org/10.1093/biolre/ioaa096
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author Anderson, Deborah J
Politch, Joseph A
Cone, Richard A
Zeitlin, Larry
Lai, Samuel K
Santangelo, Philip J
Moench, Thomas R
Whaley, Kevin J
author_facet Anderson, Deborah J
Politch, Joseph A
Cone, Richard A
Zeitlin, Larry
Lai, Samuel K
Santangelo, Philip J
Moench, Thomas R
Whaley, Kevin J
author_sort Anderson, Deborah J
collection PubMed
description Sexually transmitted infections are highly prevalent, and over 40% of pregnancies are unplanned. We are producing new antibody-based multipurpose prevention technology products to address these problems and fill an unmet need in female reproductive health. We used a Nicotiana platform to manufacture monoclonal antibodies against two prevalent sexually transmitted pathogens, HIV-1 and HSV-2, and incorporated them into a vaginal film (MB66) for preclinical and Phase 1 clinical testing. These tests are now complete and indicate that MB66 is effective and safe in women. We are now developing an antisperm monoclonal antibody to add contraceptive efficacy to this product. The antisperm antibody, H6-3C4, originally isolated by Shinzo Isojima from the blood of an infertile woman, recognizes a carbohydrate epitope on CD52g, a glycosylphosphatidylinositol-anchored glycoprotein found in abundance on the surface of human sperm. We engineered the antibody for production in Nicotiana; the new antibody which we call “human contraception antibody,” effectively agglutinates sperm at concentrations >10 μg/ml and maintains activity under a variety of physiological conditions. We are currently seeking regulatory approval for a Phase 1 clinical trial, which will include safety and “proof of principle” efficacy endpoints. Concurrently, we are working with new antibody production platforms to bring the costs down, innovative antibody designs that may produce more effective second-generation antibodies, and delivery systems to provide extended protection.
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spelling pubmed-74013872020-09-30 Engineering monoclonal antibody-based contraception and multipurpose prevention technologies(†) Anderson, Deborah J Politch, Joseph A Cone, Richard A Zeitlin, Larry Lai, Samuel K Santangelo, Philip J Moench, Thomas R Whaley, Kevin J Biol Reprod Contraceptive Special Issue Sexually transmitted infections are highly prevalent, and over 40% of pregnancies are unplanned. We are producing new antibody-based multipurpose prevention technology products to address these problems and fill an unmet need in female reproductive health. We used a Nicotiana platform to manufacture monoclonal antibodies against two prevalent sexually transmitted pathogens, HIV-1 and HSV-2, and incorporated them into a vaginal film (MB66) for preclinical and Phase 1 clinical testing. These tests are now complete and indicate that MB66 is effective and safe in women. We are now developing an antisperm monoclonal antibody to add contraceptive efficacy to this product. The antisperm antibody, H6-3C4, originally isolated by Shinzo Isojima from the blood of an infertile woman, recognizes a carbohydrate epitope on CD52g, a glycosylphosphatidylinositol-anchored glycoprotein found in abundance on the surface of human sperm. We engineered the antibody for production in Nicotiana; the new antibody which we call “human contraception antibody,” effectively agglutinates sperm at concentrations >10 μg/ml and maintains activity under a variety of physiological conditions. We are currently seeking regulatory approval for a Phase 1 clinical trial, which will include safety and “proof of principle” efficacy endpoints. Concurrently, we are working with new antibody production platforms to bring the costs down, innovative antibody designs that may produce more effective second-generation antibodies, and delivery systems to provide extended protection. Oxford University Press 2020-08 2020-06-08 /pmc/articles/PMC7401387/ /pubmed/32607584 http://dx.doi.org/10.1093/biolre/ioaa096 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Society for the Study of Reproduction. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Contraceptive Special Issue
Anderson, Deborah J
Politch, Joseph A
Cone, Richard A
Zeitlin, Larry
Lai, Samuel K
Santangelo, Philip J
Moench, Thomas R
Whaley, Kevin J
Engineering monoclonal antibody-based contraception and multipurpose prevention technologies(†)
title Engineering monoclonal antibody-based contraception and multipurpose prevention technologies(†)
title_full Engineering monoclonal antibody-based contraception and multipurpose prevention technologies(†)
title_fullStr Engineering monoclonal antibody-based contraception and multipurpose prevention technologies(†)
title_full_unstemmed Engineering monoclonal antibody-based contraception and multipurpose prevention technologies(†)
title_short Engineering monoclonal antibody-based contraception and multipurpose prevention technologies(†)
title_sort engineering monoclonal antibody-based contraception and multipurpose prevention technologies(†)
topic Contraceptive Special Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401387/
https://www.ncbi.nlm.nih.gov/pubmed/32607584
http://dx.doi.org/10.1093/biolre/ioaa096
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