Department of Oncology, Ludwig Institute for Cancer Research Lausanne, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Immunol Rev. 2023 Nov;320(1):166-198. doi: 10.1111/imr.13252. Epub 2023 Aug 7.
Adoptive T-cell transfer (ACT) therapies, including of tumor infiltrating lymphocytes (TILs) and T cells gene-modified to express either a T cell receptor (TCR) or a chimeric antigen receptor (CAR), have demonstrated clinical efficacy for a proportion of patients and cancer-types. The field of ACT has been driven forward by the clinical success of CD19-CAR therapy against various advanced B-cell malignancies, including curative responses for some leukemia patients. However, relapse remains problematic, in particular for lymphoma. Moreover, for a variety of reasons, relative limited efficacy has been demonstrated for ACT of non-hematological solid tumors. Indeed, in addition to pre-infusion challenges including lymphocyte collection and manufacturing, ACT failure can be attributed to several biological processes post-transfer including, (i) inefficient tumor trafficking, infiltration, expansion and retention, (ii) chronic antigen exposure coupled with insufficient costimulation resulting in T-cell exhaustion, (iii) a range of barriers in the tumor microenvironment (TME) mediated by both tumor cells and suppressive immune infiltrate, (iv) tumor antigen heterogeneity and loss, or down-regulation of antigen presentation machinery, (v) gain of tumor intrinsic mechanisms of resistance such as to apoptosis, and (vi) various forms of toxicity and other adverse events in patients. Affinity-optimized TCRs can improve T-cell function and innovative CAR designs as well as gene-modification strategies can be used to coengineer specificity, safety, and function into T cells. Coengineering strategies can be designed not only to directly support the transferred T cells, but also to block suppressive barriers in the TME and harness endogenous innate and adaptive immunity. Here, we review a selection of the remarkable T-cell coengineering strategies, including of tools, receptors, and gene-cargo, that have been developed in recent years to augment tumor control by ACT, more and more of which are advancing to the clinic.
过继性 T 细胞转移(ACT)疗法,包括肿瘤浸润淋巴细胞(TIL)和基因修饰表达 T 细胞受体(TCR)或嵌合抗原受体(CAR)的 T 细胞,已经证明了对一部分患者和癌症类型的临床疗效。ACT 领域的发展得益于 CD19-CAR 疗法在各种晚期 B 细胞恶性肿瘤中的临床成功,包括一些白血病患者的治愈反应。然而,复发仍然是一个问题,特别是对于淋巴瘤。此外,由于各种原因,ACT 对非血液学实体肿瘤的疗效相对有限。事实上,除了输注前的挑战,包括淋巴细胞的采集和制造之外,ACT 失败还可以归因于转移后包括以下几个生物学过程:(i)肿瘤转移、浸润、扩增和保留效率低下,(ii)慢性抗原暴露与不足的共刺激导致 T 细胞衰竭,(iii)肿瘤微环境(TME)中的一系列障碍,这些障碍既由肿瘤细胞介导,也由抑制性免疫浸润细胞介导,(iv)肿瘤抗原异质性和丢失或抗原呈递机制下调,(v)肿瘤内在的耐药机制获得,如凋亡,以及(vi)患者中出现各种形式的毒性和其他不良反应。亲和力优化的 TCR 可以改善 T 细胞的功能,创新的 CAR 设计以及基因修饰策略可以用于共工程特异性、安全性和功能到 T 细胞中。共工程策略不仅可以设计为直接支持转移的 T 细胞,还可以阻断 TME 中的抑制性障碍,并利用内源性先天和适应性免疫。在这里,我们回顾了近年来开发的一些显著的 T 细胞共工程策略,包括工具、受体和基因载体,这些策略旨在通过 ACT 增强肿瘤控制,其中越来越多的策略正在进入临床。