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引用次数: 0
摘要
抗肿瘤嵌合抗原受体(CAR)疗法的有效性主要取决于 CAR 细胞对靶细胞敏感性的提高。然而,CAR疗法也会产生非特异性副作用:靶外肿瘤毒性。CAR 细胞的敏感性和特异性是其他细胞识别靶细胞过程中最重要的特性。目前的发展主要集中在探索分子生物学方法,以设计具有最高灵敏度的 CAR 细胞,而 CAR 细胞的特异性问题却很少被考虑。为了评估 CAR 细胞的特异性,我们建议除了提高 CAR 抗原的亲和力外,还应考虑 CAR 的集群能力。我们假设 CAR 细胞的细胞毒性由 CAR 聚类决定。后者在成核理论的框架内进行处理。我们得出了 CAR 细胞细胞毒性概率的主方程。临界 CAR 簇的大小是两个最基本的参数之一。探讨了必要敏感性和充分特异性的条件。得出了相关的参数图。讨论了该方法在评估开发中的 CAR 疗法特异性方面的可能应用。
The method for assessing the specificity of developing CAR therapies.
The effectiveness of antitumor chimeric antigen receptor (CAR) therapy mainly dealt with an elevated sensitivity of CAR cells to target cells. However, CAR therapies are associated with nonspecific side effects: on-target off-tumor toxicity. Sensitivity and specificity of CAR cells are the most important properties of the recognition process of target cells among other cells. Current developments are mainly concentrated on exploring molecular biology methods for designing CAR cells with the highest sensitivity, while the problem of the CAR cell specificity is rarely considered. For the assessment of CAR cell specificity, we suggest that, in addition to an elevated level of CAR-antigen affinity, the ability of CARs for clustering should be taken into account. We assume that the CAR cell cytotoxicity is determined by CAR clustering. The latter is treated within the framework of nucleation theory. The master equation for the probability of CAR cell cytotoxicity is derived. The size of a critical CAR cluster is found to be one of two most essential parameters. The conditions for necessary sensitivity and sufficient specificity are explored. Relevant parametric diagrams are derived. Possible applications of the method for assessing the specificity of developing CAR therapies are discussed.