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利用固有免疫增强溶瘤癌症免疫疗法。

Exploiting Preexisting Immunity to Enhance Oncolytic Cancer Immunotherapy.

机构信息

Drug Research Program ImmunoViroTherapy Lab (IVT), Faculty of Pharmacy iCAN Digital Precision Cancer Medicine Flagship, Helsinki University, Viikinkaari 5E, Finland.

Faculty of Science, Leiden University, Leiden, the Netherlands.

出版信息

Cancer Res. 2020 Jun 15;80(12):2575-2585. doi: 10.1158/0008-5472.CAN-19-2062. Epub 2020 Feb 27.

Abstract

Because of the high coverage of international vaccination programs, most people worldwide have been vaccinated against common pathogens, leading to acquired pathogen-specific immunity with a robust memory T-cell repertoire. Although CD8 antitumor cytotoxic T lymphocytes (CTL) are the preferred effectors of cancer immunotherapy, CD4 T-cell help is also required for an optimal antitumor immune response to occur. Hence, we investigated whether the pathogen-related CD4 T-cell memory populations could be reengaged to support the CTLs, converting a weak primary antitumor immune response into a stronger secondary one. To this end, we used our PeptiCRAd technology that consists of an oncolytic adenovirus coated with MHC-I-restricted tumor-specific peptides and developed it further by introducing pathogen-specific MHC-II-restricted peptides. Mice preimmunized with tetanus vaccine were challenged with B16.OVA tumors and treated with the newly developed hybrid TT-OVA-PeptiCRAd containing both tetanus toxoid- and tumor-specific peptides. Treatment with the hybrid PeptiCRAd significantly enhanced antitumor efficacy and induced TT-specific, CD40 ligand-expressing CD4 T helper cells and maturation of antigen-presenting cells. Importantly, this approach could be extended to naturally occurring tumor peptides (both tumor-associated antigens and neoantigens), as well as to other pathogens beyond tetanus, highlighting the usefulness of this technique to take full advantage of CD4 memory T-cell repertoires when designing immunotherapeutic treatment regimens. Finally, the antitumor effect was even more prominent when combined with the immune checkpoint inhibitor anti-PD-1, strengthening the rationale behind combination therapy with oncolytic viruses. SIGNIFICANCE: These findings establish a novel technology that enhances oncolytic cancer immunotherapy by capitalizing on pre-acquired immunity to pathogens to convert a weak antitumor immune response into a much stronger one.

摘要

由于国际疫苗接种计划的高覆盖率,世界上大多数人都接种了针对常见病原体的疫苗,从而产生了针对病原体的特异性免疫,具有强大的记忆 T 细胞库。虽然 CD8 抗肿瘤细胞毒性 T 淋巴细胞(CTL)是癌症免疫治疗的首选效应物,但 CD4 T 细胞辅助对于发生最佳抗肿瘤免疫反应也是必需的。因此,我们研究了病原体相关的 CD4 T 细胞记忆群体是否可以重新被激活以支持 CTL,从而将较弱的原发性抗肿瘤免疫反应转化为更强的继发性免疫反应。为此,我们使用了我们的 PeptiCRAd 技术,该技术由涂有 MHC-I 限制性肿瘤特异性肽的溶瘤腺病毒组成,并通过引入病原体特异性 MHC-II 限制性肽进一步开发了该技术。用破伤风疫苗进行预免疫的小鼠接受 B16.OVA 肿瘤的挑战,并接受新开发的含有破伤风类毒素和肿瘤特异性肽的杂交 TT-OVA-PeptiCRAd 治疗。用杂交 PeptiCRAd 治疗显著增强了抗肿瘤疗效,并诱导了 TT 特异性、表达 CD40 配体的 CD4 T 辅助细胞和抗原呈递细胞的成熟。重要的是,这种方法可以扩展到天然存在的肿瘤肽(包括肿瘤相关抗原和新抗原)以及破伤风以外的其他病原体,这突出了这种技术在设计免疫治疗方案时充分利用 CD4 记忆 T 细胞库的有用性。最后,当与免疫检查点抑制剂抗 PD-1 联合使用时,抗肿瘤效果更为显著,这加强了溶瘤病毒联合治疗的合理性。

意义

这些发现建立了一种新的技术,通过利用对病原体的预先获得的免疫来增强溶瘤癌症免疫治疗,从而将较弱的抗肿瘤免疫反应转化为更强的免疫反应。

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