Pampusch Mary S, Skinner Pamela J
Department of Veterinary and Biomedical Sciences, University of Minnesota.
Department of Veterinary and Biomedical Sciences, University of Minnesota;
J Vis Exp. 2020 Mar 18(157). doi: 10.3791/60400.
Emerging immunotherapies to treat infectious diseases and cancers often involve transduction of cellular populations with genes encoding disease-targeting proteins. For example, chimeric antigen receptor (CAR)-T cells to treat cancers and viral infections involve the transduction of T cells with synthetic genes encoding CAR molecules. The CAR molecules make the T cells specifically recognize and kill cancer or virally infected cells. Cells can also be co-transduced with other genes of interest. For example, cells can be co-transduced with genes encoding proteins that target cells to specific locations. Here, we present a protocol to transduce primary peripheral blood mononuclear cells (PBMCs) with genes encoding a virus-specific CAR and the B cell follicle homing molecule chemokine receptor type 5 (CXCR5). This procedure takes nine days and results in transduced T cell populations that maintain a central memory phenotype. Maintenance of a central memory or less differentiated phenotype has been shown to associate with persistence of cells post-infusion. Furthermore, cells produced with this method show high levels of viability, high levels of co-expression of the two transduced genes, and large enough quantities of cells for immunotherapeutic infusion. This nine-day protocol may be broadly used for CAR-T cell and other T cell immunotherapy approaches. The methods described here are based on studies presented in our previous publications.
用于治疗传染病和癌症的新兴免疫疗法通常涉及用编码疾病靶向蛋白的基因转导细胞群体。例如,用于治疗癌症和病毒感染的嵌合抗原受体(CAR)-T细胞涉及用编码CAR分子的合成基因转导T细胞。CAR分子使T细胞特异性识别并杀死癌症或病毒感染的细胞。细胞也可以与其他感兴趣的基因共转导。例如,细胞可以与编码将细胞靶向特定位置的蛋白质的基因共转导。在这里,我们展示了一种用编码病毒特异性CAR和B细胞滤泡归巢分子5型趋化因子受体(CXCR5)的基因转导原代外周血单核细胞(PBMC)的方案。这个过程需要九天时间,并产生保持中央记忆表型的转导T细胞群体。已证明维持中央记忆或低分化表型与输注后细胞的持久性相关。此外,用这种方法产生的细胞显示出高活力、两个转导基因的高共表达水平,以及足够数量的细胞用于免疫治疗输注。这个九天的方案可广泛用于CAR-T细胞和其他T细胞免疫治疗方法。这里描述的方法基于我们以前出版物中提出的研究。