Dragu Laura Denisa, Chivu-Economescu Mihaela, Pitica Ioana Madalina, Matei Lilia, Bleotu Coralia, Diaconu Carmen Cristina, Necula Laura Georgiana
Stefan S. Nicolau Institute of Virology, 030304 Bucharest, Romania.
Faculty of Medicine, Titu Maiorescu University, 040051 Bucharest, Romania.
Curr Issues Mol Biol. 2025 Jul 8;47(7):525. doi: 10.3390/cimb47070525.
This manuscript assesses the critical role of exosomal PD-L1 (ExoPD-L1) in immune suppression, tumor progression, and resistance to therapy. ExoPD-L1 has been identified as a key mediator of tumor immune evasion, contributing to systemic immunosuppression beyond the tumor microenvironment (TME) due to its capacity to travel to distant anatomical sites. In this context, the review aims to elaborate on the mechanisms by which exosomal PD-L1 interacts with T cell receptors and modulates both the tumor microenvironment and immune responses, impacting patient outcomes. We further explore emerging therapeutic strategies that target ExoPD-L1 to enhance the effectiveness of immunotherapy. Blocking ExoPD-L1 offers a novel approach to counteracting immune escape in cancer. Promising strategies include inhibiting exosome biogenesis with GW4869 or Rab inhibitors, neutralizing ExoPD-L1 with targeted antibodies, and silencing PD-L1 expression through RNA interference (RNAi) or CRISPR-based methods. While each approach presents certain limitations, their integration into combination therapies holds significant potential to improve the efficacy of immune checkpoint inhibitors. Future research should focus on optimizing these strategies for clinical application, with particular attention to improving delivery specificity and minimizing off-target effects.
本手稿评估了外泌体程序性死亡配体1(ExoPD-L1)在免疫抑制、肿瘤进展和治疗耐药性中的关键作用。ExoPD-L1已被确定为肿瘤免疫逃逸的关键介质,由于其能够转移至远处解剖部位,它会导致肿瘤微环境(TME)之外的全身免疫抑制。在此背景下,本综述旨在阐述外泌体PD-L1与T细胞受体相互作用并调节肿瘤微环境和免疫反应从而影响患者预后的机制。我们进一步探索了针对ExoPD-L1以提高免疫治疗效果的新兴治疗策略。阻断ExoPD-L1为对抗癌症免疫逃逸提供了一种新方法。有前景的策略包括用GW4869或Rab抑制剂抑制外泌体生物发生、用靶向抗体中和ExoPD-L1以及通过RNA干扰(RNAi)或基于CRISPR的方法使PD-L1表达沉默。虽然每种方法都有一定局限性,但将它们整合到联合治疗中具有显著潜力来提高免疫检查点抑制剂的疗效。未来研究应专注于优化这些策略以用于临床应用,尤其要注意提高递送特异性并最小化脱靶效应。