Li Tan, Li Bo, Lin Liteng, Chen Gengjia, Wang Xiaobin, Chen Ye, Huang Wensou, Cai Mingyue, Shuai Xintao, Zhu Kangshun
Department of Minimally Invasive Interventional Radiology, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, China.
Nanomedicine Research Center, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, China.
J Control Release. 2024 Dec;376:913-929. doi: 10.1016/j.jconrel.2024.10.069. Epub 2024 Nov 6.
Microwave ablation (MWA) is a frequently adopted regional therapy for treating hepatocellular carcinoma (HCC) in clinic. However, incomplete microwave ablation (IMWA) is often inevitable due to the restraint of ablating large tumors or tumors in special locations, resulting in a high recurrence rate of HCC. Moreover, the most promising immune checkpoint blockade (ICB)-based immunotherapy is raising hindered by the toxicity and insufficient immune response. To overcome these barriers, we conjugate small nanovesicle (smDV)-derived from matured dendritic cells (mDCs) with anti-CTLA-4 antibody (smDV-aCTLA-4) using a metabolic tagging technology, which could trigger the infiltration of cytotoxic T cells (CTLs) and adopted tumor-infiltrating lymphocytes (TILs) in residual HCC after IMWA. In HCC microenvironment, the administration of smDV-aCTLA-4 could promote antigen presentation and immune checkpoint suppression to activate CTLs and improve the safety of anti-CTLA-4 antibody. Moreover, the anti-tumor efficacy of CTLs elicited by smDV-aCTLA-4 could also be further enhanced by anti-programmed death 1 (aPD-1) antibody. In addition, compared to the adoptive TILs therapy, the treatment using smDV-aCTLA-4-bonded TILs (smDV-aCTLA-4@TILs) could promote the proliferation and infiltration of cytotoxic TILs in residual HCC after IMWA. Our results clearly evidenced the potency of a new type of engineered DC nanovesicles in reducing HCC recurrence after IMWA.
微波消融(MWA)是临床上治疗肝细胞癌(HCC)常用的局部治疗方法。然而,由于在消融大肿瘤或特殊位置肿瘤时受到限制,不完全微波消融(IMWA)往往不可避免,导致HCC复发率较高。此外,最有前景的基于免疫检查点阻断(ICB)的免疫疗法因毒性和免疫反应不足而受到阻碍。为了克服这些障碍,我们使用代谢标记技术将源自成熟树突状细胞(mDCs)的小纳米囊泡(smDV)与抗CTLA-4抗体(smDV-aCTLA-4)偶联,这可以促使细胞毒性T细胞(CTLs)浸润,并在IMWA后使肿瘤浸润淋巴细胞(TILs)进入残留的HCC中。在HCC微环境中,给予smDV-aCTLA-4可促进抗原呈递和免疫检查点抑制,从而激活CTLs并提高抗CTLA-4抗体的安全性。此外,smDV-aCTLA-4引发的CTLs的抗肿瘤功效还可通过抗程序性死亡1(aPD-1)抗体进一步增强。此外,与过继性TILs疗法相比,使用smDV-aCTLA-4结合的TILs(smDV-aCTLA-4@TILs)进行治疗可促进IMWA后残留HCC中细胞毒性TILs的增殖和浸润。我们的结果清楚地证明了一种新型工程化树突状细胞纳米囊泡在降低IMWA后HCC复发方面的潜力。