Tan Xu, Wang Yu, Long Lei, Chen Hongdan, Qu Langfan, Cao Xiaohui, Li Huijuan, Chen Zelin, Luo Shenglin, Shi Chunmeng
Institute of Rocket Force Medicine, State Key Laboratory of Trauma and Chemical Poisoning, College of Preventive Medicine, Army Medical University, Gaotanyan Street 30, Chongqing 400038, China.
Department of Breast and Thyroid Surgery, Chongqing General Hospital, Xingguang Road 118, Chongqing 401121, China.
Pharmacol Res. 2024 Dec;210:107489. doi: 10.1016/j.phrs.2024.107489. Epub 2024 Nov 5.
Cancer immunotherapy remains a low immune response rate in clinic because of dominant immunosuppressive tumor microenvironment (TME) and lack of effective drug to specifically remodel the TME. In this work, we introduced a tumor-seeking human serum albumin (HSA) based delivery platform by covalently conjugating with a tumor-targeting near-infrared (NIR) photosensitizer (IR-DBI) and non-covalently loading of immune modulator Resiquimod (R848). HSA exhibited tumor-preferential accumulation after covalent conjugation with IR-DBI. Meanwhile, HSA restricted the rotation of IR-DBI, narrowed the HOMO-LUMO energy gap, significantly enhanced fluorescent intensity and dual-modal phototherapy (PTT/PDT). The enhanced phototherapeutic effect further induced robust ICD effect. More importantly, non-covalent loading of R848 could be released from HSA at tumor sites by laser irradiation-induced heat. The in-situ release of R848 in TME efficiently promoted the maturation of DC cells and repolarized M2 macrophages to M1 macrophages. Consequently, robust photo-induced antitumor immunity was triggered in the different mice models bearing primary and distant tumors or lung metastasis, which was further enhanced by combining with CTLA-4 blockade therapy. Taken together, this work may present a versatile albumin composite which exhibits tumor-preferential accumulation and imaging-guided PDT/PTT/immunotherapy.
由于占主导地位的免疫抑制性肿瘤微环境(TME)以及缺乏特异性重塑TME的有效药物,癌症免疫疗法在临床上的免疫应答率仍然较低。在这项工作中,我们通过将肿瘤靶向近红外(NIR)光敏剂(IR-DBI)共价偶联以及非共价负载免疫调节剂瑞喹莫德(R848),引入了一种基于肿瘤靶向人血清白蛋白(HSA)的递送平台。与IR-DBI共价偶联后,HSA表现出肿瘤优先积累。同时,HSA限制了IR-DBI的旋转,缩小了HOMO-LUMO能隙,显著增强了荧光强度以及双模态光疗(PTT/PDT)。增强的光疗效果进一步诱导了强大的免疫原性细胞死亡(ICD)效应。更重要的是,R848的非共价负载可以通过激光照射诱导的热量在肿瘤部位从HSA中释放出来。R848在TME中的原位释放有效地促进了树突状细胞(DC)的成熟,并使M2巨噬细胞重新极化到M1巨噬细胞。因此,在携带原发性和远处肿瘤或肺转移的不同小鼠模型中触发了强大的光诱导抗肿瘤免疫,通过与抗细胞毒性T淋巴细胞相关蛋白4(CTLA-4)阻断疗法联合使用,这种免疫进一步增强。综上所述,这项工作可能展示了一种多功能白蛋白复合材料,其具有肿瘤优先积累以及成像引导的PDT/PTT/免疫疗法。