Department of Bioengineering, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan.
Department of Immunotherapeutics, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Adv Sci (Weinh). 2023 Apr;10(10):e2205139. doi: 10.1002/advs.202205139. Epub 2023 Feb 5.
Treatment of immunologically cold tumors is a major challenge for immune checkpoint inhibitors (ICIs). Interleukin 12 (IL-12) can invigorate ICIs against cold tumors by establishing a robust antitumor immunity. However, its toxicity and systemic induction of counteracting immunosuppressive signals have hindered translation. Here, IL-12 activity is spatiotemporally controlled for safely boosting efficacy without the stimulation of interfering immune responses by generating a nanocytokine that remains inactive at physiological pH, but unleashes its full activity at acidic tumor pH. The IL-12-based nanocytokine (Nano-IL-12) accumulate and release IL-12 in tumor tissues, eliciting localized antitumoral inflammation, while preventing systemic immune response, counteractive immune reactions, and adverse toxicities even after repeated intravenous administration. The Nano-IL-12-mediated spatiotemporal control of inflammation prompt superior anticancer efficacy, and synergize with ICIs to profoundly inflame the tumor microenvironment and completely eradicate ICI-resistant primary and metastatic tumors. The strategy could be a promising approach toward safer and more effective immunotherapies.
免疫冷肿瘤的治疗是免疫检查点抑制剂(ICIs)的主要挑战。白细胞介素 12(IL-12)可以通过建立强大的抗肿瘤免疫来激活针对冷肿瘤的 ICI。然而,其毒性和全身性诱导拮抗免疫抑制信号的作用阻碍了其转化。在这里,通过生成一种在生理 pH 下保持无活性但在酸性肿瘤 pH 下释放其全部活性的纳米细胞因子,时空控制 IL-12 的活性,在不刺激干扰免疫反应的情况下安全地提高疗效。基于 IL-12 的纳米细胞因子(Nano-IL-12)在肿瘤组织中积聚并释放 IL-12,引发局部抗肿瘤炎症,同时防止全身免疫反应、拮抗免疫反应和不良反应毒性,即使在重复静脉给药后也是如此。Nano-IL-12 介导的炎症时空控制可促进卓越的抗癌疗效,并与 ICI 协同作用,强烈激发肿瘤微环境,彻底根除 ICI 抵抗的原发性和转移性肿瘤。该策略可能是一种更安全、更有效的免疫疗法的有前途的方法。