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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...

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Autores principales: Zhang, Ran, Rao, Man, Li, Chuan, Cao, Jingyuan, Meng, Qinglin, Zheng, Min, Wang, Meili, Dai, Yunping, Liang, Mifang, Li, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2009
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.
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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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