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树突状细胞疫苗二十周年——迎接下一波浪潮。

On the Twentieth Anniversary of Dendritic Cell Vaccines - Riding the Next Wave.

机构信息

Center for Cellular Immunotherapies and The Parker Institute for Cancer Immunotherapy, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Cancer Res. 2022 Mar 15;82(6):966-968. doi: 10.1158/0008-5472.CAN-21-4440.

DOI:10.1158/0008-5472.CAN-21-4440
PMID:35288731
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9744103/
Abstract

In the mid 1990's, a convergence of discoveries in dendritic cell (DC) biology and tumor antigen identification led investigators to study DCs as adjuvants for cancer vaccines. On the twentieth anniversary of a seminal clinical study by Jacques Banchereau and colleagues, we revisit the key events that prompted the initial wave of DC vaccine clinical studies and lessons learned that, in our opinion, helped forge the path for the field that we now call immuno-oncology. It is essential to recall that prior to the discovery of immune checkpoint therapy and chimeric antigen receptor (CAR) T-cell therapy, skepticism prevailed regarding the potential therapeutic benefit of immunotherapies. In hindsight, we can now appreciate how the early DC cancer vaccine trials helped investigators sustain their attention on adaptive immunity specific for malignant cells. These vaccines demonstrated clear evidence for induction of antigen-specific T cells and were well tolerated despite low rates of objective clinical response. In the context of the current era some 20 years later, harnessing DC vaccines has been shown to increase the breadth and diversity of tumor-specific T cells, and by trafficking to sites of metastases promote an inflamed tumor microenvironment. See related article by Banchereau and colleagues, Cancer Res 2001; 61:6451-8.

摘要

20 世纪 90 年代中期,树突状细胞 (DC) 生物学和肿瘤抗原鉴定方面的一系列发现促使研究人员将 DC 作为癌症疫苗的佐剂进行研究。在 Jacques Banchereau 和同事的一项开创性临床研究二十周年之际,我们回顾了促使最初一波 DC 疫苗临床研究的关键事件,以及我们认为有助于为我们现在称之为免疫肿瘤学领域铺平道路的经验教训。至关重要的是要回想一下,在发现免疫检查点疗法和嵌合抗原受体 (CAR) T 细胞疗法之前,人们对免疫疗法的潜在治疗益处持怀疑态度。事后看来,我们现在可以理解早期的 DC 癌症疫苗试验如何帮助研究人员将注意力集中在针对恶性细胞的适应性免疫上。这些疫苗清楚地证明了诱导抗原特异性 T 细胞的能力,并且尽管客观临床反应率较低,但耐受性良好。在大约 20 年后的当前时代背景下,利用树突状细胞疫苗已被证明可以增加肿瘤特异性 T 细胞的广度和多样性,并通过向转移部位转移来促进炎症肿瘤微环境。见 Banchereau 和同事的相关文章,Cancer Res 2001; 61:6451-8。

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