Miltenyi Biotec B.V. & Co. KG, 51429 Bergisch Gladbach, Germany.
Cells. 2024 Nov 14;13(22):1880. doi: 10.3390/cells13221880.
CAR T cell therapy has been an effective treatment option for hematological malignancies. However, the therapeutic potential of CAR T cells can be reduced by several constraints, partly due to immunogenicity and toxicities. The lack of established workflows enabling thorough evaluation of new candidates, limits comprehensive CAR assessment. To improve the selection of lead CAR candidates, we established a stringent, multistep workflow based on specificity assessments, employing multiple assays and technologies. Moreover, we characterized a human FOLR1-directed CAR binding domain. Selection of binding domains was based on extensive specificity assessment by flow cytometry and imaging, to determine on-/off-target and off-tumor reactivity. CAR T cell functionality and specificity were assessed by high-throughput screening and advanced in vitro assays. Our validation strategy highlights that assays comprehensively characterizing CAR functionality and binding specificity complement each other. Thereby, critical specificity considerations can be addressed early in the development process to overcome current limitations for future CAR T cell therapies.
嵌合抗原受体 T 细胞疗法已成为血液系统恶性肿瘤的一种有效治疗选择。然而,嵌合抗原受体 T 细胞的治疗潜力受到多种限制,部分原因是免疫原性和毒性。缺乏既定的工作流程来彻底评估新的候选者,限制了对 CAR 的全面评估。为了提高先导 CAR 候选物的选择,我们建立了一个严格的、多步骤的工作流程,该流程基于特异性评估,采用多种检测方法和技术。此外,我们还对人类 FOLR1 导向的 CAR 结合域进行了特征描述。结合域的选择是基于流式细胞术和成像的广泛特异性评估,以确定靶内/靶外和肿瘤外反应性。CAR T 细胞的功能和特异性通过高通量筛选和先进的体外检测进行评估。我们的验证策略强调了全面表征 CAR 功能和结合特异性的检测方法相互补充。通过这种方式,可以在开发过程的早期解决关键的特异性问题,克服未来 CAR T 细胞疗法的当前限制。