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Functional recombinant human anti-HAV antibody expressed in milk of transgenic mice
Hepatitis A virus (HAV) is a wide spread pathogenic agent and is the common cause of acute Hepatitis A worldwide. Passive immunization of HAV plays an extremely important role in post-exposure prophylaxis with clinical applications often requiring large amounts of antibody. As an alternative to the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089081/ https://www.ncbi.nlm.nih.gov/pubmed/19130282 http://dx.doi.org/10.1007/s11248-008-9241-0 |
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author | Zhang, Ran Rao, Man Li, Chuan Cao, Jingyuan Meng, Qinglin Zheng, Min Wang, Meili Dai, Yunping Liang, Mifang Li, Ning |
author_facet | Zhang, Ran Rao, Man Li, Chuan Cao, Jingyuan Meng, Qinglin Zheng, Min Wang, Meili Dai, Yunping Liang, Mifang Li, Ning |
author_sort | Zhang, Ran |
collection | PubMed |
description | Hepatitis A virus (HAV) is a wide spread pathogenic agent and is the common cause of acute Hepatitis A worldwide. Passive immunization of HAV plays an extremely important role in post-exposure prophylaxis with clinical applications often requiring large amounts of antibody. As an alternative to the in vitro production of recombinant proteins, expression of monoclonal antibodies (mAbs) in the milk of transgenic animals is currently used being associated with low production costs and high activity. In this paper, eight founder lines of transgenic mice were generated by co-microinjection of the two cassettes encoding the heavy- and light-chains of a neutralizing anti-HAV antibody, respectively. The expressed heavy- and light-chains of the mAb were correctly assembled and modified in the mammary gland as detected by western blotting. High expression levels of the antibody were achieved during the lactation period and found to be independent of the copy numbers of integrated transgenes. The highest level was up to 32.2 mg/ml. The binding specificity and neutralizing activity of the expressed mAb were assayed by ELISA and neutralizing test, showing that it is capable to neutralize the JN strain of Hepatitis A virus efficiently. Therefore, our results suggest that a large-scale and efficient production of the anti-HAV mAb in the milk of transgenic farm animals would be feasible in the future. |
format | Online Article Text |
id | pubmed-7089081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-70890812020-03-23 Functional recombinant human anti-HAV antibody expressed in milk of transgenic mice Zhang, Ran Rao, Man Li, Chuan Cao, Jingyuan Meng, Qinglin Zheng, Min Wang, Meili Dai, Yunping Liang, Mifang Li, Ning Transgenic Res Original Paper Hepatitis A virus (HAV) is a wide spread pathogenic agent and is the common cause of acute Hepatitis A worldwide. Passive immunization of HAV plays an extremely important role in post-exposure prophylaxis with clinical applications often requiring large amounts of antibody. As an alternative to the in vitro production of recombinant proteins, expression of monoclonal antibodies (mAbs) in the milk of transgenic animals is currently used being associated with low production costs and high activity. In this paper, eight founder lines of transgenic mice were generated by co-microinjection of the two cassettes encoding the heavy- and light-chains of a neutralizing anti-HAV antibody, respectively. The expressed heavy- and light-chains of the mAb were correctly assembled and modified in the mammary gland as detected by western blotting. High expression levels of the antibody were achieved during the lactation period and found to be independent of the copy numbers of integrated transgenes. The highest level was up to 32.2 mg/ml. The binding specificity and neutralizing activity of the expressed mAb were assayed by ELISA and neutralizing test, showing that it is capable to neutralize the JN strain of Hepatitis A virus efficiently. Therefore, our results suggest that a large-scale and efficient production of the anti-HAV mAb in the milk of transgenic farm animals would be feasible in the future. Springer Netherlands 2009-01-08 2009 /pmc/articles/PMC7089081/ /pubmed/19130282 http://dx.doi.org/10.1007/s11248-008-9241-0 Text en © Springer Science+Business Media B.V. 2009 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Paper Zhang, Ran Rao, Man Li, Chuan Cao, Jingyuan Meng, Qinglin Zheng, Min Wang, Meili Dai, Yunping Liang, Mifang Li, Ning Functional recombinant human anti-HAV antibody expressed in milk of transgenic mice |
title | Functional recombinant human anti-HAV antibody expressed in milk of transgenic mice |
title_full | Functional recombinant human anti-HAV antibody expressed in milk of transgenic mice |
title_fullStr | Functional recombinant human anti-HAV antibody expressed in milk of transgenic mice |
title_full_unstemmed | Functional recombinant human anti-HAV antibody expressed in milk of transgenic mice |
title_short | Functional recombinant human anti-HAV antibody expressed in milk of transgenic mice |
title_sort | functional recombinant human anti-hav antibody expressed in milk of transgenic mice |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089081/ https://www.ncbi.nlm.nih.gov/pubmed/19130282 http://dx.doi.org/10.1007/s11248-008-9241-0 |
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