Lobner Elisabeth, Wachernig Anna, Gudipati Venugopal, Mayrhofer Patrick, Salzer Benjamin, Lehner Manfred, Huppa Johannes B, Kunert Renate
Department of Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria.
Institute for Hygiene and Applied Immunology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Front Bioeng Biotechnol. 2020 Feb 7;8:49. doi: 10.3389/fbioe.2020.00049. eCollection 2020.
The transmembrane protein CD19 is exclusively expressed on normal and malignant B cells and therefore constitutes the target of approved CAR-T cell-based cancer immunotherapies. Current efforts to assess CAR-T cell functionality in a quantitative fashion both and are hampered by the limited availability of the properly folded recombinant extracellular domain of CD19 (CD19-ECD) considered as "difficult-to-express" (DTE) protein. Here, we successfully expressed a novel fusion construct consisting of the full-length extracellular domain of CD19 and domain 2 of human serum albumin (CD19-AD2), which was integrated into the bacterial artificial chromosome vector backbone for generation of a recombinant CHO-K1 production cell line. Product titers could be further boosted using valproic acid as a chemical chaperone. Purified monomeric CD19-AD2 proved stable as shown by non-reduced SDS-PAGE and SEC-MALS measurements. Moreover, flow cytometric analysis revealed specific binding of CD19-AD2 to CD19-CAR-T cells. Finally, we demonstrate biological activity of our CD19-AD2 fusion construct as we succeeded in stimulating CD19-CAR-T cells effectively with the use of CD19-AD2-decorated planar supported lipid bilayers.
跨膜蛋白CD19仅在正常和恶性B细胞上表达,因此成为已获批的基于嵌合抗原受体T细胞(CAR-T)的癌症免疫疗法的靶点。目前,定量评估CAR-T细胞功能的工作受到了阻碍,因为被视为“难以表达”(DTE)蛋白的正确折叠的重组细胞外结构域CD19(CD19-ECD)的可用性有限。在此,我们成功表达了一种新型融合构建体,其由CD19的全长细胞外结构域和人血清白蛋白的结构域2(CD19-AD2)组成,该构建体被整合到细菌人工染色体载体骨架中,用于生成重组CHO-K1生产细胞系。使用丙戊酸作为化学伴侣可进一步提高产物滴度。经非还原SDS-PAGE和多角度激光散射尺寸排阻色谱(SEC-MALS)测量表明,纯化的单体CD19-AD2是稳定的。此外,流式细胞术分析显示CD19-AD2与CD19-CAR-T细胞存在特异性结合。最后,我们成功地使用装饰有CD19-AD2的平面支撑脂质双层有效地刺激了CD19-CAR-T细胞,从而证明了我们的CD19-AD2融合构建体具有生物活性。