Developing macrophage reprogramming mRNA nanocarriers for initial clinical testing

项目摘要 肿瘤相关巨噬细胞（TAM）通常表达M2表型，这使得它们能够执行 免疫抑制和促肿瘤功能。将这些TAM重编程为M1表型 可以阻碍它们的促癌活性并释放抗肿瘤免疫力，但目前实现这一目标的努力 是非特异性的并引起全身炎症。我们在弗雷德哈钦森癌症研究中心的小组 开发了一种靶向纳米载体，可以在体外转录编码M1极化的mRNA， 转录因子重编程TAM而不引起全身毒性。目标是设计第一个 我们在这里提出了一项用这种纳米药物治疗化疗耐药卵巢癌患者的临床试验。 将生成IND申请所需数据的研究。具体而言，我们将（1）开发一个强大的 在GMP下大规模生产遗传巨噬细胞编程纳米颗粒的方案- 条件，以便他们可以进行大型灵长类动物和人类研究，（2）确定潜在的输注 反应风险，参考FDA对纳米医学的规定，和（3）确认纳米颗粒的安全性 用于大型动物物种的临床应用。我们希望拟议研究的结果将有助于推动这一进程。 探讨晚期卵巢癌治疗的临床实践，并为设计 一种广泛的纳米治疗药物，将基因重编程TAM作为治疗其他肿瘤的策略 类型

Project Summary Tumor-associated macrophages (TAMs) usually express an M2 phenotype which enables them to perform immunosuppressive and tumor-promoting functions. Reprogramming these TAMs toward an M1 phenotype could thwart their pro-cancer activities and unleash anti-tumor immunity, but current efforts to accomplish this are nonspecific and elicit systemic inflammation. Our group at Fred Hutchinson Cancer Research Center has developed a targeted nanocarrier that can deliver in vitro-transcribed mRNA encoding M1-polarizing transcription factors to reprogram TAMs without causing systemic toxicity. With the goal of designing the first clinical trial for treating chemotherapy-resistant ovarian cancer patients with this nanodrug, we propose here research that will generate the data required for an IND application. Specifically, we will (1) develop a robust protocol for the scaled-up production of genetic macrophage-programming nanoparticles under GMP- conditions so they can be carried forward into large primate and human studies, (2) identify potential infusion reaction risks, with reference to FDA regulations for nanomedicines, and (3) confirm safety of the nanoparticles for clinical use in a large-animal species. We expect the outcome of the proposed research will help propel this approach into clinical practice for the treatment of advanced ovarian cancer, and provide knowledge to design a broad repertoire of nanotherapeutics that genetically reprogram TAMs as a strategy to treat other tumor types.