Vito Alyssa, Rathmann Stephanie, Mercanti Natalie, El-Sayes Nader, Mossman Karen, Valliant John
Department of Medicine, McMaster Immunology Research Centre, McMaster University, Hamilton, ON L8S 4K1, Canada.
Department of Chemistry and Chemical Biology, McMaster University, Hamilton, ON L8S 4K1, Canada.
Int J Mol Sci. 2021 May 3;22(9):4843. doi: 10.3390/ijms22094843.
Triple negative breast cancer (TNBC) is an aggressive subtype of the disease with poor clinical outcomes and limited therapeutic options. Immune checkpoint blockade (CP) has surged to the forefront of cancer therapies with widespread clinical success in a variety of cancer types. However, the percentage of TNBC patients that benefit from CP as a monotherapy is low, and clinical trials have shown the need for combined therapeutic modalities. Specifically, there has been interest in combining CP therapy with radiation therapy where clinical studies primarily with external beam have suggested their therapeutic synergy, contributing to the development of anti-tumor immunity. Here, we have developed a therapeutic platform combining radionuclide therapy (RT) and immunotherapy utilizing a radiolabeled biomolecule and CP in an E0771 murine TNBC tumor model. Survival studies show that while neither monotherapy is able to improve therapeutic outcomes, the combination of RT + CP extended overall survival. Histologic analysis showed that RT + CP increased necrotic tissue within the tumor and decreased levels of F4/80+ macrophages. Flow cytometry analysis of the peripheral blood also showed that RT + CP suppressed macrophages and myeloid-derived suppressive cells, both of which actively contribute to immune escape and tumor relapse.
三阴性乳腺癌(TNBC)是一种侵袭性疾病亚型,临床预后较差且治疗选择有限。免疫检查点阻断(CP)已跃居癌症治疗前沿,在多种癌症类型中取得了广泛的临床成功。然而,作为单一疗法受益于CP的TNBC患者比例较低,临床试验表明需要联合治疗方式。具体而言,人们对将CP疗法与放射疗法相结合很感兴趣,主要采用外照射的临床研究表明了它们的治疗协同作用,有助于抗肿瘤免疫的发展。在此,我们在E0771小鼠TNBC肿瘤模型中开发了一种结合放射性核素疗法(RT)和免疫疗法的治疗平台,利用放射性标记的生物分子和CP。生存研究表明,虽然单一疗法均无法改善治疗效果,但RT + CP联合治疗可延长总生存期。组织学分析表明,RT + CP增加了肿瘤内的坏死组织,并降低了F4/80+巨噬细胞水平。外周血的流式细胞术分析还表明,RT + CP抑制了巨噬细胞和髓系来源的抑制细胞,这两种细胞均积极促成免疫逃逸和肿瘤复发。