Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
Adv Exp Med Biol. 2021;1290:67-80. doi: 10.1007/978-3-030-55617-4_4.
The great hopes raised by the discovery of the immunoregulatory cytokine interleukin 12 (IL-12) as an anticancer agent were marred during early clinical experimentation because of severe adverse effects, which prompted a search for alternative formulations and routes of administration. Onco-immunotherapeutic viruses (OIVs) are wild-type or genetically engineered viruses that exert antitumor activity by causing death of the tumor cells they infect and by overcoming a variety of immunosuppressive mechanisms put in place by the tumors. OIVs have renewed the interest in IL-12, as they offer the opportunity to encode the cytokine transgenically from the viral genome and to produce it at high concentrations in the tumor bed. A large body of evidence indicates that IL-12 serves as a potent adjuvant for the immunotherapeutic response elicited by OIVs in murine tumor models. The list of OIVs includes onco-immunotherapeutic herpes simplex, adeno, measles, Newcastle disease, and Maraba viruses, among others. The large increase in IL-12-mediated adjuvanticity was invariably observed for all the OIVs analyzed. Indirect evidence suggests that locally delivered IL-12 may also increase tumor antigenicity. Importantly, the OIV/IL-12 treatment was not accompanied by adverse effects and elicited a long-lasting immune response capable of halting the growth of distant tumors. Thus, OIVs provide an avenue for reducing the clinical toxicity associated with systemic IL-12 therapy, by concentrating the cytokine at the site of disease. The changes to the tumor microenvironment induced by the IL-12-armed OIVs primed the tumors to an improved response to the checkpoint blockade therapy, suggesting that the triple combination is worth pursuing in the future. The highly encouraging results in preclinical models have prompted translation to the clinic. How well the IL-12-OIV-checkpoint inhibitors' combination will perform in humans remains to be fully investigated.
免疫调节细胞因子白细胞介素 12(IL-12)作为一种抗癌药物的发现带来了巨大的希望,但在早期临床实验中,由于严重的不良反应,这一希望破灭了,这促使人们寻找替代制剂和给药途径。溶瘤免疫治疗病毒(OIVs)是野生型或基因工程病毒,通过引起感染肿瘤细胞的死亡以及克服肿瘤产生的多种免疫抑制机制,发挥抗肿瘤活性。OIVs 重新引起了人们对白细胞介素 12 的兴趣,因为它们提供了从病毒基因组中转基因编码细胞因子并在肿瘤床中高浓度产生它的机会。大量证据表明,白细胞介素 12 作为 OIVs 在小鼠肿瘤模型中引发的免疫治疗反应的有效佐剂。OIVs 的列表包括溶瘤免疫治疗单纯疱疹、腺病毒、麻疹、新城疫和马利巴病毒等。分析的所有 OIVs 都观察到白细胞介素 12 介导的佐剂作用大大增加。间接证据表明,局部给予白细胞介素 12 也可能增加肿瘤抗原性。重要的是,OIV/IL-12 治疗没有伴随不良反应,并引发了持久的免疫反应,能够阻止远处肿瘤的生长。因此,OIVs 通过将细胞因子集中在疾病部位,为减少与全身 IL-12 治疗相关的临床毒性提供了一种途径。IL-12 武装的 OIVs 对肿瘤微环境的改变使肿瘤对检查点阻断治疗的反应得到改善,这表明三重组合值得在未来进一步研究。临床前模型中非常令人鼓舞的结果促使其转化为临床研究。IL-12-OIV-检查点抑制剂组合在人类中的表现如何仍有待充分研究。