Department of Korean Medicine, College of Korean Medicine, Kyung Hee University, Seoul, Republic of Korea.
Exp Mol Med. 2023 Sep;55(9):1996-2004. doi: 10.1038/s12276-023-01080-3. Epub 2023 Sep 1.
Within the tumor microenvironment (TME), regulatory T cells (Tregs) play a key role in suppressing anticancer immune responses; therefore, various strategies targeting Tregs are becoming important for tumor therapy. To prevent the side effects of nonspecific Treg depletion, such as immunotherapy-related adverse events (irAEs), therapeutic strategies that specifically target Tregs in the TME are being investigated. Tumor-targeting drug conjugates are efficient drugs in which a cytotoxic payload is assembled into a carrier that binds Tregs via a linker. By allowing the drug to act selectively on target cells, this approach has the advantage of increasing the therapeutic effect and minimizing the side effects of immunotherapy. Antibody-drug conjugates, immunotoxins, peptide-drug conjugates, and small interfering RNA conjugates are being developed as Treg-targeting drug conjugates. In this review, we discuss key themes and recent advances in drug conjugates targeting Tregs in the TME, as well as future design strategies for successful use of drug conjugates for Treg targeting in immunotherapy.
在肿瘤微环境(TME)中,调节性 T 细胞(Tregs)在抑制抗肿瘤免疫反应方面发挥着关键作用;因此,针对 Tregs 的各种策略正成为肿瘤治疗的重要手段。为了防止非特异性 Treg 耗竭的副作用,如免疫治疗相关不良事件(irAEs),正在研究专门针对 TME 中 Tregs 的治疗策略。肿瘤靶向药物偶联物是一种高效药物,其中细胞毒性有效载荷与通过连接子与 Tregs 结合的载体组装在一起。通过允许药物选择性地作用于靶细胞,这种方法具有提高治疗效果和最小化免疫治疗副作用的优点。抗体药物偶联物、免疫毒素、肽药物偶联物和小干扰 RNA 偶联物被开发为针对 Tregs 的药物偶联物。在这篇综述中,我们讨论了针对 TME 中 Tregs 的药物偶联物的关键主题和最新进展,以及用于免疫治疗中 Treg 靶向的成功使用药物偶联物的未来设计策略。