PROTAC 工程化蛋白/DNA 纳米抗原是癌症免疫治疗中树突状细胞疫苗的有效增强剂
PROTAC-Engineered Protein/DNA Nanoantigen is a Potent Booster for Dendritic Cell Vaccines in Cancer Immunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Hydrogel/nanoadjuvant-mediated combined cell vaccines for cancer immunotherapy.
Hydrogel/nanoadjuvant-mediated combined cell vaccines for cancer immunotherapy.
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肿瘤全细胞和树突状细胞(DCs)的联合细胞疫苗为恶性肿瘤提供了一种有效的个体化免疫治疗。我们提出了一种创新策略,称为“生物材料介导的联合细胞疫苗免疫治疗”,该策略将肿瘤细胞疫苗和DC疫苗与环糊精-聚乙二醇水凝胶和胞嘧啶-磷酸-鸟嘌呤(CpG)纳米佐剂相结合。该纳米佐剂通过抗原和佐剂的共递送促进抗原呈递并增强免疫激发效力。水凝胶支架为注射的外源性DCs提供了更好的生长微环境,并招募内源性DCs以维持其活力,从而产生协同效应。
结果表明,相对于活肿瘤细胞,免疫原性死亡的肿瘤细胞在免疫佐剂CpG纳米颗粒的辅助作用下有效激活了DC成熟。T细胞百分比、增殖能力、细胞因子分泌和细胞毒性效应的增加揭示了联合细胞疫苗增强的免疫原性。联合水凝胶/纳米佐剂系统在抑制肿瘤生长方面表现出最佳效率。
此外,单剂量接种基于水凝胶的联合疫苗显著延缓了肿瘤的发展。生物材料介导的联合细胞疫苗显著增加了效应T细胞的浸润,缓解了瘤内免疫抑制微环境,并最大化了疫苗的免疫效应,从而改善了癌症免疫治疗。意义声明:基于细胞的疫苗,包括肿瘤全细胞疫苗或DC疫苗,作为癌症免疫治疗的有效方法已引起广泛关注。
然而,由于肿瘤全细胞疫苗免疫原性低以及转移的DC疫苗存活期短,在临床试验中难以获得令人满意的结果。因此,提高细胞疫苗诱导强效且持久免疫应答的能力是疫苗开发的首要目标。生物材料介导的联合细胞疫苗是一种创新的癌症免疫治疗策略。联合水凝胶/纳米佐剂系统包含免疫原性死亡的肿瘤细胞、DC和纳米佐剂。负载纳米佐剂的免疫原性死亡肿瘤细胞可作为肿瘤细胞疫苗诱导有效的免疫应答。基于水凝胶的联合肿瘤细胞/DC疫苗可用于个体化免疫治疗。
Combined cell vaccines of tumor whole cells and dendritic cells (DCs) provide an effective individualized immunotherapy for malignant tumors.
We propose an innovative strategy termed "biomaterial-mediated combined cell vaccines for immunotherapy," which combines tumor cell and DC vaccines with a cyclodextrin-polyethylene glycol hydrogel and a cytosine-phosphate-guanine (CpG) nanoadjuvant. The nanoadjuvant promotes antigen presentation and amplifies immune-eliciting potency by co-delivery of antigens and adjuvants. The hydrogel scaffold provides a better growth microenvironment for injected exogenous DCs and recruits endogenous DCs to maintain their viability for synergistic effect.
The results indicated that, relative to live tumor cells, the immunogenically dying tumor cells activated DC maturation effectively with the auxiliary effect of immune adjuvant CpG nanoparticles. The increased T cell percentage, proliferation ability, cytokine secretion, and cytotoxic effect revealed the enhanced immunogenicity of the combined cell vaccines. The combined hydrogel/nanoadjuvant system showed the best efficiency in inhibiting tumor growth.
Moreover, vaccination with a single dose of hydrogel-based combined vaccines significantly delayed the development of tumors. The biomaterial-mediated combined cell vaccines remarkably increased the infiltration of effector T cells, alleviated the intratumoral immunosuppressive microenvironment, and maximized the immune effect of the vaccines, thus improving cancer immunotherapy. STATEMENT OF SIGNIFICANCE: Cell-based vaccines, including tumor whole-cell vaccine or DC vaccine, have attracted wide attention as an effective method for cancer immunotherapy.
However, it is difficult to gain satisfactory outcomes in clinical trials because of the low immunogenicity of tumor whole cell vaccine and the short-term survival of transferred DC vaccine.
Therefore, improving the ability of cell-based vaccines to induce a strong and durable immune response is the primary objective for vaccine development. Biomaterial-mediated combined cell vaccines is an innovative strategy for cancer immunotherapy.
The combined hydrogel/ nanoadjuvant system comprises immunogenically dying tumor cells, DCs, and nanoadjuvants. Nanoadjuvant-loaded immunogenically dying tumor cells can induce efficient immune response as the tumor cell vaccine. The hydrogel-based combined tumor cell/DC vaccine could be used for individualized immunotherapy.
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