Pojar Kimberly, Reckendorfer Diana, Strauss Judith, Szaffich Sarah, Ahmadi-Erber Sarah, Schippers Timo, Berraondo Pedro, Orlinger Klaus K, Raguz Josipa, Lauterbach Henning
Hookipa Pharma Inc, New York, NY, USA.
Program of Immunology and Immunotherapy, Cima Universidad de Navarra, Pamplona, Spain.
Oncoimmunology. 2025 Dec;14(1):2514040. doi: 10.1080/2162402X.2025.2514040. Epub 2025 Jun 10.
Among the plethora of cancer immune evasion mechanisms, T-cell-inhibiting factors within the tumor microenvironment impose a major challenge for the development of novel immunotherapies. Strategies to overcome immunosuppression and remodel the TME are therefore urgently needed. Therapeutic cancer vaccines based on engineered arenaviruses have been proven to generate potent tumor specific CD8+ T-cell responses in preclinical models and cancer patients. Despite signs of clinical activity as monotherapy, combination therapies are needed to further increase the therapeutic effect. To address this need, we evaluated the efficacy of recombinant vectors based on lymphocytic choriomeningitis virus encoding the T-cell stimulating cytokines IL-7, IL-12 and IL-15 with or without tumor-associated antigens. These vectors were tested in three different mouse tumor models (TC-1, MC-38 and B16.F10). Our results demonstrate that only IL-12 encoding vectors led to increased immunogenicity and efficacy, which, after systemic administration, was associated with adverse events. The safest and most potent regimen consisted of systemic vaccination with tumor antigen encoding vectors and local injection of IL-12-encoding vectors. A single round of this treatment regimen resulted in 86-100% tumor-free mice and warrants further investigation.
在众多癌症免疫逃逸机制中,肿瘤微环境中的T细胞抑制因子对新型免疫疗法的开发构成了重大挑战。因此,迫切需要克服免疫抑制和重塑肿瘤微环境的策略。基于工程化沙粒病毒的治疗性癌症疫苗已被证明在临床前模型和癌症患者中能产生强大的肿瘤特异性CD8+T细胞反应。尽管单药治疗有临床活性迹象,但仍需要联合疗法来进一步提高治疗效果。为满足这一需求,我们评估了基于淋巴细胞脉络丛脑膜炎病毒的重组载体的疗效,这些载体编码T细胞刺激细胞因子IL-7、IL-12和IL-15,有无肿瘤相关抗原。这些载体在三种不同的小鼠肿瘤模型(TC-1、MC-38和B16.F10)中进行了测试。我们的结果表明,只有编码IL-12的载体能提高免疫原性和疗效,全身给药后,这与不良事件有关。最安全、最有效的方案是用编码肿瘤抗原的载体进行全身疫苗接种,并局部注射编码IL-12的载体。一轮这种治疗方案导致86-100%的小鼠无肿瘤,值得进一步研究。