Functional recombinant human anti-HAV antibody expressed in milk of transgenic mice

被引:16
|
作者
Zhang, Ran [2 ]
Rao, Man [2 ]
Li, Chuan [1 ]
Cao, Jingyuan [1 ]
Meng, Qinglin [1 ]
Zheng, Min [3 ]
Wang, Meili [3 ]
Dai, Yunping [2 ]
Liang, Mifang [1 ]
Li, Ning [2 ]
机构
[1] China CDC, Natl Inst Viral Dis Control & Prevent, State Key Lab Infect Dis Control & Prevent, Beijing 100052, Peoples R China
[2] China Agr Univ, State Key Lab Agrobiotechnol, Beijing 100193, Peoples R China
[3] Beijing Genprotein Biotechnol Co, Beijing 100193, Peoples R China
关键词
Hepatitis A virus; Monoclonal antibody; Transgenic mice; Milk; HEPATITIS-A VIRUS; MONOCLONAL-ANTIBODIES; NEUTRALIZING ANTIBODIES; MAMMARY-GLAND; PROTEINS; ANIMALS;
D O I
10.1007/s11248-008-9241-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:445 / 453
页数:9
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