TILT Biotherapeutics Ltd, Helsinki, Finland.
Department of Pathology, Faculty of Medicine, Cancer Gene Therapy Group, University of Helsinki, Finland.
Int J Cancer. 2017 Oct 1;141(7):1458-1468. doi: 10.1002/ijc.30839. Epub 2017 Jun 29.
Systemic high dose interleukin-2 (IL-2) postconditioning has long been utilized in boosting the efficacy of T cells in adoptive cell therapy (ACT) of solid tumors. The resulting severe off-target toxicity of these regimens renders local production at the tumor an attractive concept with possible safety gains. We evaluated the efficacy and safety of intratumorally administered IL-2-coding adenoviruses in combination with tumor-infiltrating lymphocyte therapy in syngeneic Syrian hamsters bearing HapT1 pancreatic tumors and with T cell receptor transgenic ACT in B16.OVA melanoma bearing C57BL/6 mice. The models are complementary: hamsters are semi-permissive for human oncolytic adenovirus, whereas detailed immunological analyses are possible in mice. In both models, local production of IL-2 successfully replaced the need for systemic recombinant IL-2 (rIL-2) administration and increased the efficacy of the cell therapy. Furthermore, vectored delivery of IL-2 significantly enhanced the infiltration of CD8+ T cells, M1-like macrophages, and B-cells while systemic rIL-2 increased CD25 + FoxP3+ T cells at the tumor. In contrast with vectored delivery, histopathological analysis of systemic rIL-2-treated animals revealed significant changes in lungs, livers, hearts, spleens, and kidneys. In summary, local IL-2 production results in efficacy and safety gains in the context of ACT. These preclinical assessments provide the rationale for ongoing clinical translation.
全身大剂量白细胞介素-2(IL-2)后处理长期以来一直被用于增强过继细胞疗法(ACT)中 T 细胞对实体瘤的疗效。这些方案产生的严重的脱靶毒性使得在肿瘤局部产生 IL-2 成为一个有吸引力的概念,可能具有安全性优势。我们评估了肿瘤内给予编码白细胞介素-2 的腺病毒与肿瘤浸润淋巴细胞治疗联合应用于携带 HapT1 胰腺肿瘤的同种叙利亚仓鼠和 T 细胞受体转基因 ACT 治疗 B16.OVA 黑色素瘤的荷瘤 C57BL/6 小鼠的疗效和安全性。这些模型是互补的:仓鼠对半许可的人溶瘤腺病毒具有一定的抗性,而在小鼠中可以进行详细的免疫学分析。在这两种模型中,IL-2 的局部产生成功取代了对全身重组白细胞介素-2(rIL-2)给药的需求,并提高了细胞治疗的疗效。此外,载体传递的 IL-2 显著增强了 CD8+T 细胞、M1 样巨噬细胞和 B 细胞的浸润,而全身 rIL-2 增加了肿瘤中的 CD25+FoxP3+T 细胞。与载体传递相比,全身给予 rIL-2 治疗的动物的组织病理学分析显示肺部、肝脏、心脏、脾脏和肾脏发生了显著变化。总之,ACT 中局部 IL-2 的产生可带来疗效和安全性的提高。这些临床前评估为正在进行的临床转化提供了依据。