Kast Florian, Klein Christian, Umaña Pablo, Gros Alena, Gasser Stephan
Roche Pharma Research & Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Vall d'Hebron Institute of Oncology, Cellex Center, Barcelona, Spain.
Oncoimmunology. 2021 Jan 7;10(1):1869389. doi: 10.1080/2162402X.2020.1869389.
Based on the success of tumor-infiltrating lymphocytes (TIL)-based therapies, personalized adoptive cell therapies (ACT) targeting neoantigens have the potential to become a disruptive technology and lead to highly effective treatments for cancer patients for whom no other options exist. ACT of TIL, peripheral blood or gene-engineered peripheral blood lymphocytes (PBLs) targeting neoantigens is a highly personalized intervention that requires three discrete steps: i) Identification of suitable personal targets (neoantigens), ii) selection of T cells or their T cell receptors (TCRs) that are specific for the identified neoantigens and iii) expansion of the selected T cell population or generation of sufficient number of TCR modified T cells. In this review, we provide an introduction into challenges and approaches to identify neoantigens and to select the Adoptive Cell Therapy, ACT, Neoantigen, T cell, Cancer respective neoantigen-reactive T cells for use in ACT.
基于肿瘤浸润淋巴细胞(TIL)疗法的成功,针对新抗原的个性化过继性细胞疗法(ACT)有潜力成为一项颠覆性技术,并为没有其他治疗选择的癌症患者带来高效治疗方案。以TIL、外周血或基因工程改造的外周血淋巴细胞(PBL)为基础针对新抗原的ACT是一种高度个性化的干预措施,需要三个不同步骤:i)识别合适的个人靶点(新抗原);ii)选择对已识别新抗原具有特异性的T细胞或其T细胞受体(TCR);iii)扩增所选T细胞群体或产生足够数量的TCR修饰T细胞。在本综述中,我们介绍了识别新抗原以及为ACT选择相应新抗原反应性T细胞的挑战和方法。