Immunobiology Laboratory, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Melchor Fernández Almagro, 3, 28029, Madrid, Spain.
Division of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), University of Navarra, and Instituto de Investigación Sanitaria de Navarra (IdISNA), Pamplona, Spain.
J Immunother Cancer. 2019 Apr 8;7(1):100. doi: 10.1186/s40425-019-0565-5.
The manipulation of dendritic cells (DCs) for cancer vaccination has not reached its full potential, despite the revolution in cancer immunotherapy. DCs are fundamental for CD8+ T cell activation, which relies on cross-presentation of exogenous antigen on MHC-I and can be fostered by immunogenic cancer cell death. Translational and clinical research has focused on in vitro-generated monocyte-derived DCs, while the vaccination efficacy of natural conventional type 1 DCs (cDC1s), which are associated with improved anti-tumor immunity and specialize on antigen cross-presentation, remains unknown.
We isolated primary spleen mouse cDC1s and established a protocol for fast ex vivo activation and antigen-loading with lysates of tumor cells that underwent immunogenic cell death by UV irradiation. Natural tumor antigen-loaded cDC1s were transferred and their potential for induction of endogenous CD8+ and CD4+ T cell responses in vivo, cancer prevention and therapy were assessed in three grafted cancer models. Further, we tested the efficacy of natural cDC1 vaccination in combination and comparison with anti-PD-1 treatment in two "wildtype" tumor models not expressing exogenous antigens.
Herein, we reveal that primary mouse cDC1s ex vivo loaded with dead tumor cell-derived antigen are activated and induce strong CD8+ T cell responses from the endogenous repertoire upon adoptive transfer in vivo through tumor antigen cross-presentation. Notably, cDC1-based vaccines enhance tumor infiltration by cancer-reactive CD8+ and CD4+ T cells and halt progression of engrafted cancer models, including tumors that are refractory to anti-PD-1 treatment. Moreover, combined tumor antigen-loaded primary cDC1 and anti-PD-1 therapy had strong synergistic effects in a PD-1 checkpoint inhibition susceptible cancer model.
This preclinical proof-of-principle study is first to support the therapeutic efficacy of cancer immunotherapy with syngeneic dead tumor cell antigen-loaded mouse cDC1s, the equivalents of the human dendritic cell subset that correlates with beneficial prognosis of cancer patients. Our data pave the way for translation of cDC1-based cancer treatments into the clinic when isolation of natural human cDC1s becomes feasible.
尽管癌症免疫疗法取得了革命性进展,但树突状细胞(DC)在癌症疫苗接种中的应用尚未充分发挥其潜力。DC 是 CD8+T 细胞激活的基础,这依赖于 MHC-I 上外源抗原的交叉呈递,并且可以通过免疫原性的癌细胞死亡来促进。转化和临床研究集中在体外生成的单核细胞衍生的 DC 上,而与改善抗肿瘤免疫和专门从事抗原交叉呈递相关的天然常规 1 型 DC(cDC1)的疫苗接种效果仍不清楚。
我们分离了原代脾脏小鼠 cDC1,并建立了一种方案,用于快速离体激活和负载经紫外线照射发生免疫原性细胞死亡的肿瘤细胞裂解物。天然肿瘤抗原负载的 cDC1 被转移,并在三种移植的癌症模型中评估了其在体内诱导内源性 CD8+和 CD4+T 细胞反应、预防和治疗癌症的潜力。此外,我们还测试了天然 cDC1 疫苗接种与两种不表达外源抗原的“野生型”肿瘤模型中抗 PD-1 治疗相结合的疗效。
在此,我们揭示了经体外负载死肿瘤细胞衍生抗原的原代小鼠 cDC1 通过肿瘤抗原交叉呈递在体内被激活,并在过继转移后诱导强烈的 CD8+T 细胞反应来自内源性库。值得注意的是,cDC1 为基础的疫苗通过癌症反应性 CD8+和 CD4+T 细胞增强肿瘤浸润,并阻止植入的癌症模型的进展,包括对抗 PD-1 治疗有抗性的肿瘤。此外,负载肿瘤抗原的原代 cDC1 与抗 PD-1 治疗联合具有协同作用,在 PD-1 检查点抑制敏感的癌症模型中具有强大的协同作用。
这项临床前原理验证研究首次支持使用同源性死肿瘤细胞抗原负载的小鼠 cDC1 进行癌症免疫治疗的疗效,这是与癌症患者有利预后相关的人类树突状细胞亚群的等效物。我们的数据为 cDC1 为基础的癌症治疗转化为临床铺平了道路,当分离天然人类 cDC1 成为可行时。