Department of Pathology, Johns Hopkins University, Baltimore, MD 21287, USA.
Department of Oncology, Johns Hopkins University, Baltimore, MD 21287, USA.
J Immunol Res. 2021 Nov 8;2021:7855808. doi: 10.1155/2021/7855808. eCollection 2021.
Interleukin 2 (IL-2) plays a fundamental role in both immune activation and tolerance and has revolutionized the field of cancer immunotherapy since its discovery. The ability of IL-2 to mediate tumor regression in preclinical and clinical settings led to FDA approval for its use in the treatment of metastatic renal cell carcinoma and metastatic melanoma in the 1990s. Although modest success is observed in the clinic, cancer patients receiving IL-2 therapy experience a wide array of side effects ranging from flu-like symptoms to life-threatening conditions such as vascular leak syndrome. Over the past three decades, efforts have focused on circumventing IL-2-related toxicities by engineering methods to localize IL-2 to the tumor or secondary lymphoid tissue, preferentially activate CD8 T cells and NK cells, and alter pharmacokinetic properties to increase bioavailability. This review summarizes the various IL-2-based strategies that have emerged, with a focus on chimeric fusion methods.
白细胞介素 2(IL-2)在免疫激活和耐受中发挥着重要作用,自发现以来,它彻底改变了癌症免疫治疗领域。IL-2 介导肿瘤消退的能力在临床前和临床环境中得到证实,这促使 FDA 在 20 世纪 90 年代批准其用于治疗转移性肾细胞癌和转移性黑色素瘤。尽管在临床上取得了一定的成功,但接受 IL-2 治疗的癌症患者会出现一系列副作用,从流感样症状到血管渗漏综合征等危及生命的情况。在过去的三十年中,人们一直致力于通过工程方法将 IL-2 定位到肿瘤或次级淋巴组织,优先激活 CD8 T 细胞和 NK 细胞,并改变药代动力学特性以提高生物利用度,从而规避与 IL-2 相关的毒性。这篇综述总结了各种基于 IL-2 的策略,重点介绍了嵌合融合方法。