Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices , Soochow University , 199 Ren'ai Rd , Suzhou , Jiangsu 215123 , P. R. China.
Bioconjug Chem. 2019 Aug 21;30(8):2115-2126. doi: 10.1021/acs.bioconjchem.9b00245. Epub 2019 Aug 6.
The development of effective cancer vaccines is an important direction in the area of cancer immunotherapy. Although certain types of preventive cancer vaccines have already been used in the clinic, therapeutic cancer vaccines for treatment of already established tumors are still in high demand. In this study, we develop a new type of cancer vaccine by mixing cell-penetrating peptide (CPP) conjugated antigen as the enhanced antigen, together with CpG as the immune adjuvant. A special CPP, cytosol-localizing internalization peptide 6 (CLIP6), which has the ability to enter cells exclusively via a nonendosomal mechanism, i.e., direct translocation across the cell membrane, is conjugated with model antigen ovalbumin (OVA). Compared to naked OVA, the obtained CLIP6-OVA conjugates show greatly increased uptake by dendritic cells (DCs) and, more importantly, remarkably enhanced antigen cross-presentation, eliciting stronger cytotoxic T lymphocyte (CTL) mediated immune responses with the help of CpG. This CLIP6-OVA/CpG formulation offers effective protection for mice against challenged B16-OVA tumors, and is able to further function as a therapeutic vaccine, which, in combination with immune checkpoint blockade therapy, can significantly suppress the already-established tumors. Such a CLIP6-based cancer vaccine developing strategy shows promising potential toward clinical practice owing to its features of easy preparation, low cost, and remarkable biocompatibility.
开发有效的癌症疫苗是癌症免疫治疗领域的一个重要方向。虽然某些类型的预防性癌症疫苗已经在临床上使用,但用于治疗已建立的肿瘤的治疗性癌症疫苗仍有很高的需求。在本研究中,我们通过混合细胞穿透肽(CPP)缀合抗原作为增强抗原,与 CpG 作为免疫佐剂,开发了一种新型癌症疫苗。一种特殊的 CPP,即细胞质定位内化肽 6(CLIP6),具有通过非内体机制(即直接跨细胞膜易位)专门进入细胞的能力,与模型抗原卵清蛋白(OVA)缀合。与裸 OVA 相比,所得的 CLIP6-OVA 缀合物显示出大大增加的树突状细胞(DC)摄取,更重要的是,显著增强了抗原交叉呈递,在 CpG 的帮助下引发更强的细胞毒性 T 淋巴细胞(CTL)介导的免疫反应。这种 CLIP6-OVA/CpG 制剂为小鼠提供了针对挑战 B16-OVA 肿瘤的有效保护,并能够进一步用作治疗性疫苗,与免疫检查点阻断治疗结合使用,可显著抑制已建立的肿瘤。由于其易于制备、成本低和显著的生物相容性等特点,基于 CLIP6 的癌症疫苗开发策略显示出有希望的临床应用潜力。