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在肿瘤部位产生白细胞介素-2 的腺病毒消除了过继细胞治疗中全身预处理的需要。

Adenoviral production of interleukin-2 at the tumor site removes the need for systemic postconditioning in adoptive cell therapy.

机构信息

TILT Biotherapeutics Ltd, Helsinki, Finland.

Department of Pathology, Faculty of Medicine, Cancer Gene Therapy Group, University of Helsinki, Finland.

出版信息

Int J Cancer. 2017 Oct 1;141(7):1458-1468. doi: 10.1002/ijc.30839. Epub 2017 Jun 29.

Abstract

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.

摘要

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。

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