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通过p53突变定制免疫疗法使免疫难治性卵巢肿瘤致敏

Sensitizing Immune-Refractory Ovarian Tumors via p53 Mutation-Tailored Immunotherapy.

作者信息

Chatterjee Rishita, Simoni-Nieves Arturo, Truong An, Lindzen Moshit, Ozmen Furkan, Cherry Christopher, Zwicky Pascale, Mukherjee Saptaparna, Selvadurai Boobash-Raj, Salame Tomer-Meir, Gupta Nitin, Giri Suvendu, Kramarski Lior, Avraham Yahel, Weizman Eviatar, Ozmen Tugba, Noronha Ashish, Chakrabarti Priyasmita, Ramesh-Kumar Deepthi, Downward Julian, Dahan Rony, Amit Ido, Velculescu Victor, Brenton James, Mills Gordon, Oren Moshe, Yarden Yosef

机构信息

Department of Immunology and Regenerative Biology, Systems immunology, Weizmann Institute of Science, Rehovot, 76100, Israel.

Cancer Research UK and Department of Oncology, University of Cambridge Cambridge, UK.

出版信息

bioRxiv. 2025 Jun 27:2025.06.23.661120. doi: 10.1101/2025.06.23.661120.

Abstract

High-grade serous ovarian cancer demonstrates limited responsiveness to immune checkpoint inhibitors, owing in part to immunosuppressive environments shaped by nearly universal p53 aberrations. Utilizing an immunocompetent mouse model and individual p53 mutations, we identified a dependence of the p53-R270H mutation (equivalent of human R273H) on regulatory T cells (Tregs) and the PD-1/PD-L1 axis. Analysis of patient datasets associated R273H with elevated levels of two p53 targets, PD-L1 and amphiregulin (AREG), a Tregs growth factor. In contrast to p53-R172H tumors, where there was limited activity, dual antibody therapy targeting AREG and PD-L1 selectively and effectively inhibited R270H tumors. This involved polarization toward M1 macrophages, infiltration of CD8+ T cells, diminished Ly6G+ neutrophils and downregulation of interleukin-4. In patient-derived R273C organoids, the combination treatment reduced the CD4/CD8 ratio. This study is the first to establish a mutation-tailored therapeutic approach that leverages the capacity of p53 to modulate immunosuppressive mechanisms.

摘要

高级别浆液性卵巢癌对免疫检查点抑制剂的反应有限,部分原因是几乎普遍存在的p53畸变所形成的免疫抑制环境。利用具有免疫活性的小鼠模型和单个p53突变,我们确定了p53-R270H突变(相当于人类R273H)对调节性T细胞(Tregs)和PD-1/PD-L1轴的依赖性。对患者数据集的分析将R273H与两个p53靶点(PD-L1和双调蛋白(AREG),一种Tregs生长因子)的水平升高相关联。与活性有限的p53-R172H肿瘤不同,靶向AREG和PD-L1的双抗体疗法选择性且有效地抑制了R270H肿瘤。这涉及向M1巨噬细胞极化、CD8+T细胞浸润、Ly6G+中性粒细胞减少以及白细胞介素-4下调。在患者来源的R273C类器官中,联合治疗降低了CD4/CD8比率。本研究首次建立了一种针对突变的治疗方法,该方法利用p53调节免疫抑制机制的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b0/12262552/e5bdba23bfe7/nihpp-2025.06.23.661120v1-f0001.jpg

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