IL-21 武装增强了单纯治疗和联合治疗中溶瘤痘苗病毒的抗肿瘤活性。
IL-21 arming potentiates the anti-tumor activity of an oncolytic vaccinia virus in monotherapy and combination therapy.
机构信息
Shanghai Public Health Clinical Center & Institutes of Biomedical Sciences, Shanghai Medical College, Fudan University, Shanghai, China.
Shanghai Public Health Clinical Center & Institutes of Biomedical Sciences, Shanghai Medical College, Fudan University, Shanghai, China
出版信息
J Immunother Cancer. 2021 Jan;9(1). doi: 10.1136/jitc-2020-001647.
BACKGROUND
Oncolytic viruses (OVs) have shown promise in containing cancer progression in both animal models and clinical trials. How to further improve the efficacy of OVs are intensively explored. Arming OVs with immunoregulatory molecules has emerged as an important means to enhance their oncolytic activities majorly based on the mechanism of reverting the immunosuppressive nature of tumor environment. In this study, we aimed to identify the optimal combination of different OVs and immunomodulatory molecules for solid tumor treatment as well as the underlying mechanism, and subsequently evaluated its potential synergy with other immunotherapies.
METHODS
Panels of oncolytic viruses and cells stably expressing immunoregulatory molecules were separately evaluated for treating solid tumors in mouse model. A tumor-targeted replicating vaccinia virus Tian Tan strain with deletion of TK gene (TTVΔTK) was armed rationally with IL-21 to create rTTVΔTK-IL21 through recombination. CAR-T cells and iNKT cells were generated from human peripheral blood mononuclear cells. The impact of rTTVΔTK-IL21 on tumor-infiltrating lymphocytes was assessed by flow cytometry, and its therapeutic efficacy as monotherapy or in combination with CAR-T and iNKT therapy was assessed in mouse tumor models.
RESULTS
IL-21 and TTV was respectively identified as most potent immunomodulatory molecule and oncolytic virus for solid tumor suppression in mouse models. A novel recombinant oncolytic virus that resulted from their combination, namely rTTVΔTK-mIL21, led to significant tumor regression in mice, even for noninjected distant tumor. Mechanistically, rTTV∆TK-mIL21 induced a selective enrichment of immune effector cells over Treg cells and engage a systemic response of therapeutic effect. Moreover, its human form showed a notable synergy with CAR-T or iNKT therapy for tumor treatment when coupled in humanized mice.
CONCLUSION
With a strong potency of shaping tumor microenvironment toward favoring TIL activities, rTTVΔTK-IL21 represents a new opportunity worthy of further exploration in clinical settings for solid tumor control, particularly in combinatorial strategies with other immunotherapies.
ONE SENTENCE SUMMARY
IL21-armed recombinant oncolytic vaccinia virus has potent anti-tumor activities as monotherapy and in combination with other immunotherapies.
背景
溶瘤病毒(OVs)在动物模型和临床试验中均显示出抑制癌症进展的潜力。如何进一步提高 OV 的疗效,是目前研究的热点。为了增强 OV 的溶瘤活性,将免疫调节分子武装到 OV 上已成为一种重要手段,其主要机制是逆转肿瘤微环境的免疫抑制特性。在这项研究中,我们旨在确定用于实体瘤治疗的最佳 OV 和免疫调节分子组合,以及潜在的协同作用机制,并进一步评估其与其他免疫疗法联合应用的潜力。
方法
我们分别使用一系列溶瘤病毒和稳定表达免疫调节分子的细胞在小鼠模型中评估其治疗实体瘤的效果。我们通过重组技术,将缺失 TK 基因的肿瘤靶向复制型痘苗病毒天坛株(TTVΔTK)合理武装 IL-21,构建成 rTTVΔTK-IL21。CAR-T 细胞和 iNKT 细胞从人外周血单核细胞中生成。通过流式细胞术评估 rTTVΔTK-IL21 对肿瘤浸润淋巴细胞的影响,并在小鼠肿瘤模型中评估其作为单一药物或与 CAR-T 和 iNKT 联合治疗的疗效。
结果
IL-21 和 TTV 分别被鉴定为在小鼠模型中抑制实体瘤生长最有效的免疫调节分子和溶瘤病毒。它们的组合产生的新型重组溶瘤病毒,即 rTTVΔTK-mIL21,可显著抑制小鼠肿瘤生长,甚至对未注射的远处肿瘤也有抑制作用。机制上,rTTV∆TK-mIL21 诱导免疫效应细胞选择性富集,同时减少 Treg 细胞,引发全身性治疗效果。此外,当将其与 CAR-T 或 iNKT 疗法联合用于人源化小鼠的肿瘤治疗时,其在人类形式下显示出明显的协同作用。
结论
rTTVΔTK-IL21 具有强大的重塑肿瘤微环境的能力,有利于 TIL 活性,为实体瘤控制提供了新的临床应用机会,特别是与其他免疫疗法联合应用。
一句话总结
携带 IL21 的重组溶瘤痘苗病毒具有强大的抗肿瘤活性,可作为单一药物或与其他免疫疗法联合应用。