Production of human blood group B antigen epitope conjugated protein in Escherichia coli and utilization of the adsorption blood group B antibody

Wenjing Shang(Shandong University), Yafei Zhai(Shandong University), Zhongrui Ma(Shandong University), Gongjin Yang(Shandong University), Yan Ding(Shandong University), Donglei Han(Shandong University), Jiang Li(Shandong University), Houcheng Zhang(Shandong University), Jun Liu(Shandong University), Peng George Wang(Shandong University), Xianwei Liu(Shandong University), Min Chen(Shandong University)
Microbial Cell Factories
August 11, 2016
Cited by 13Open Access
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Abstract

BACKGROUND: In the process of ABO-incompatible (ABOi) organ transplantation, removal of anti-A and/or B antibodies from blood plasma is a promising method to overcome hyperacute rejection and allograft loss caused by the immune response between anti-A and/or B antibodies and the A and/or B antigens in the recipient. Although there are commercial columns to do this work, the application is still limited because of the high production cost. RESULTS: In this study, the PglB glycosylation pathway from Campylobacter jejuni was exploited to produce glycoprotein conjugated with Escherichia coli O86:B7 O-antigen, which bears the blood group B antigen epitope to absorb blood group B antibody in blood. The titers of blood group B antibody were reduced to a safe level without changing the clotting function of plasma after glycoprotein absorption of B antibodies in the plasma. CONCLUSIONS: We developed a feasible strategy for the specific adsorption/removal of blood group antibodies. This method will be useful in ABOi organ transplantation and universal blood transfusion.


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