人天然噬菌体Fab抗体文库的构建及抗PD-L1噬菌体抗体的筛选

Jiangtao Gu, Raoqing Guo, Ligang Zhang, Ning Deng
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摘要

程序性死亡配体-1(Programmed Death Ligand-1, PD-L1)与程序性死亡配体-1(Programmed Death-1, PD-1)结合,是驱动T细胞功能障碍的重要靶点,导致肿瘤细胞的免疫逃逸,因此抗PD-L1抗体在肿瘤治疗中具有广阔的应用前景。为了构建庞大的天然抗体文库,我们采集了大量成人和儿童淋巴细胞。通过PCR扩增抗体轻链和Fd基因,构建库容量为4.27×10 9的Fab噬菌体抗体文库。轻链文库和Fab文库的插入率分别为90%和70%。经PCR鉴定的克隆序列显示,所分析的序列均具有唯一性,且CDR区氨基酸序列具有多样性,证明抗体文库具有良好的多样性。通过噬菌体ELISA、PCR鉴定和序列分析筛选出与PD-L1结合的阳性克隆。最终获得两个高亲和力阳性克隆。该天然噬菌体抗体文库的成功构建为筛选人PD-L1抗体提供了一种有效的方法,有望用于筛选各种抗原的人源化抗体。
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Construction of a Natural Human Fab Phage Antibody Library and Screening of Phage Antibody against PD-L1
: Programmed Death Ligand-1(PD-L1) is an important target to drive T cell dysfunction when it connects with Programmed Death-1(PD-1), leading to immune escape of tumor cells, thus anti-PD-L1 antibody shows a promising prospect in the treatment of tumor. In order to construct a large natural antibody library, we collected a large number of lymphocytes of adults and children. The light chain and Fd genes of antibody were amplified by PCR, and the Fab phage antibody library with a library capacity of 4.27×10 9 was constructed. The insertion rates of the light chain library and the Fab library were 90% and 70%, respectively. The cloned sequences identified by PCR showed that all the sequences analyzed were unique, and the amino acid sequences of the CDR regions were diverse, which proved that there was good diversity in the antibody library. The positive clones that bind to PD-L1 were screened by phage ELISA, PCR identification and sequence analysis. In the end, two high-affinity positive clones were determined. The successful construction of this natural phage antibody library provided an effective method for screening human PD-L1 antibodies, which was expected to screen humanized antibodies against various antigens.
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