Laboratory of Cancer Immunobiology, Robert W. Franz Cancer Research Center, Earle A. Chiles Research Institute, Providence Portland Medical Center, Portland, Oregon 97213, USA.
Clin Cancer Res. 2011 Nov 15;17(22):7047-57. doi: 10.1158/1078-0432.CCR-11-0951. Epub 2011 Nov 8.
We previously reported that autophagy in tumor cells plays a critical role in cross-presentation of tumor antigens and that autophagosomes are efficient antigen carriers for cross-priming of tumor-reactive CD8(+) T cells. Here, we sought to characterize further the autophagosome-enriched vaccine named DRibble (DRiPs-containing blebs), which is derived from tumor cells after inhibition of protein degradation, and to provide insights into the mechanisms responsible for their efficacy as a novel cancer immunotherapy.
DRibbles were characterized by Western blot and light or transmission electron microscopy. The efficiency of cross-presentation mediated by DRibbles was first compared with that of whole-tumor cells and pure proteins. The mechanisms of antigen cross-presentation by DRibbles were analyzed, and the antitumor efficacy of the DRibble vaccine was tested in 3LL Lewis lung tumors and B16F10 melanoma.
The DRibbles sequester both long-lived and short-lived proteins, including defective ribosomal products (DRiP), and damage-associated molecular pattern molecules exemplified by HSP90, HSP94, calreticulin, and HMGB1. DRibbles express ligands for CLEC9A, a newly described C-type lectin receptor expressed by a subset of conventional and plasmacytoid dendritic cells (DC), and cross-presentation was partially CLEC9A dependent. Furthermore, this autophagy-assisted antigen cross-presentation pathway involved both caveolae- and clathrin-mediated endocytosis and endoplasmic reticulum-associated degradation machinery. It depends on proteasome and TAP1, but not lysosome functions of antigen-presenting cells. Importantly, DCs loaded with autophagosome-enriched DRibbles can eradicate 3LL Lewis lung tumors and significantly delay the growth of B16F10 melanoma.
These data documented the unique characteristics and potent antitumor efficacy of the autophagosome-based DRibble vaccine. The efficacy of DRibble cancer vaccine will be further tested in clinical trials.
我们之前报道过肿瘤细胞中的自噬在肿瘤抗原的交叉呈递中起着关键作用,而且自噬体是肿瘤反应性 CD8+T 细胞交叉引发的有效抗原载体。在这里,我们试图进一步描述从蛋白降解抑制后的肿瘤细胞中提取的富含自噬体的疫苗 DRibble(含自噬体的泡状结构),并深入了解其作为新型癌症免疫疗法的有效性的机制。
通过 Western blot 和光镜或透射电镜观察来表征 DRibble。首先比较了 DRibble 介导的交叉呈递效率与全肿瘤细胞和纯蛋白的效率。分析了 DRibble 交叉呈递抗原的机制,并在 3LL Lewis 肺癌和 B16F10 黑色素瘤中测试了 DRibble 疫苗的抗肿瘤功效。
DRibble 可以捕获包括长寿和短寿蛋白在内的各种蛋白,包括核糖体失活产物(DRiP)以及热休克蛋白 90(HSP90)、HSP94、钙网蛋白和高迁移率族蛋白 1(HMGB1)等损伤相关分子模式分子。DRibble 表达一种新发现的 C 型凝集素受体 CLEC9A 的配体,该受体由一部分传统和浆细胞样树突状细胞(DC)表达,且部分依赖 CLEC9A 的交叉呈递。此外,这种自噬辅助的抗原交叉呈递途径涉及网格蛋白和小窝蛋白介导的内吞作用以及内质网相关降解机制。它依赖于蛋白酶体和抗原呈递细胞中的 TAP1,但不依赖于溶酶体的功能。重要的是,负载富含自噬体的 DRibble 的 DC 可以消除 3LLLewis 肺癌,并显著延缓 B16F10 黑色素瘤的生长。
这些数据记录了基于自噬体的 DRibble 疫苗的独特特征和强大的抗肿瘤功效。DRibble 癌症疫苗的疗效将在临床试验中进一步测试。