Interdisciplinary Department of Medicine, University of Bari "Aldo Moro", Bari, Italy.
Division of Medical Oncology, A.O.U. Consorziale Policlinico di Bari, Bari, Italy.
Expert Opin Biol Ther. 2024 Nov;24(11):1245-1259. doi: 10.1080/14712598.2024.2418321. Epub 2024 Nov 4.
Systemic treatment options for renal cell carcinoma (RCC) have expanded considerably in recent years, and both tyrosine kinase inhibitors and immune checkpoint inhibitors, alone or in combination, have entered the clinical arena. Adoptive cell immunotherapies have recently revolutionized the treatment of cancer and hold the promise to further advance the treatment of RCC.
In this review, we summarize the latest preclinical and clinical development in the field of adoptive cell immunotherapy for the treatment of RCC, focusing on lymphokine-activated killer (LAK) cells, cytokine-induced killer (CIK) cells, tumor-infiltrating T cells (TILs), TCR-engineered T cells, chimeric antigen receptor (CAR) T cells, and dendritic cell vaccination strategies. Perspectives on emerging cellular products including CAR NK cells, CAR macrophages, as well as γδ T cells are also included.
So far, areas of greater therapeutic success of adoptive cell therapies include the adjuvant administration of CIK cells and the transfer of anti-CD70 CAR T cells in patients with metastatic RCC. Bench to bedside and back research will be needed to overcome current limitations of adoptive cell therapies in RCC, primarily aiming at improving the safety of immune cell products, optimizing their antitumor activity and generating off-the-shelf products ready for clinical use.
近年来,肾细胞癌(RCC)的系统治疗选择有了显著的扩展,单独或联合使用的酪氨酸激酶抑制剂和免疫检查点抑制剂已经进入临床领域。过继细胞免疫疗法最近彻底改变了癌症的治疗方法,并有望进一步推进 RCC 的治疗。
在这篇综述中,我们总结了过继细胞免疫疗法治疗 RCC 领域的最新临床前和临床进展,重点介绍了淋巴因子激活的杀伤(LAK)细胞、细胞因子诱导的杀伤(CIK)细胞、肿瘤浸润性 T 细胞(TILs)、T 细胞受体(TCR)工程化 T 细胞、嵌合抗原受体(CAR)T 细胞和树突状细胞疫苗接种策略。还包括对新兴细胞产品的观点,包括 CARNK 细胞、CAR 巨噬细胞和γδ T 细胞。
到目前为止,过继细胞疗法在辅助治疗中取得了更大的疗效,包括 CIK 细胞的辅助给药和转移性 RCC 患者中抗 CD70 CAR T 细胞的转移。需要将基础到临床和再回到基础的研究相结合,以克服过继细胞疗法在 RCC 中的当前局限性,主要目的是提高免疫细胞产品的安全性、优化其抗肿瘤活性并生成可随时用于临床使用的现成产品。