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CD137 Enhancement of HPV Positive Head and Neck Squamous Cell Carcinoma Tumor Clearance

机译:CD137增强HPV阳性头颈部鳞状细胞癌肿瘤清除率

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摘要

Standard-of-care cisplatin and radiation therapy (CRT) provides significant tumor control of human papillomavirus (HPV)-mediated head and neck squamous cell carcinomas (HNSCCs); this effectiveness depends on CRT-mediated activation of the patient’s own immune system. However, despite good survival, patients suffer significant morbidity necessitating on-going studies to define novel therapies that alleviate this burden. Given the role of the immune system in tumor clearance, immune modulation may further potentiate the CRT-activated response while potentially decreasing morbidity. CD137, an inducible cell surface receptor found on activated T cells, is involved in differentiation and survival signaling in T cells upon binding of its natural partner (CD137L). A number of studies have shown the effectiveness of targeting this immune-stimulatory pathway in regards to tumor clearance. Here, we test its role in HPV+ HNSCC tumor clearance using a previously characterized mouse model. We show that amplification of this stimulatory pathway synergizes with CRT for enhanced tumor clearance. Interestingly, tumor clearance is further potentiated by local tumor cell expression of CD137L.
机译:护理标准顺铂和放射疗法(CRT)可有效控制人乳头瘤病毒(HPV)介导的头颈部鳞状细胞癌(HNSCC)的肿瘤;这种有效性取决于CRT介导的患者自身免疫系统的激活。然而,尽管生存期良好,但患者仍患有严重的疾病,因此需要进行持续的研究以定义减轻这种负担的新疗法。考虑到免疫系统在清除肿瘤中的作用,免疫调节可以进一步增强CRT激活的反应,同时可能降低发病率。 CD137是一种在活化T细胞上发现的诱导型细胞表面受体,在其天然伴侣(CD137L)结合后,参与T细胞的分化和存活信号传递。大量研究表明,针对肿瘤清除,靶向这种免疫刺激途径是有效的。在这里,我们使用先前表征的小鼠模型测试其在HPV + HNSCC肿瘤清除中的作用。我们表明,这种刺激途径的放大与CRT协同增强肿瘤清除率。有趣的是,CD137L的局部肿瘤细胞表达进一步增强了肿瘤清除率。

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