465 Synergistic approach to overcome the solid tumor microenvironment of mesothelioma with natural killer cell-focused immunotherapy

Pippa Kennedy, Q. Kile, B. Jacobson, B. Ettestad, Sarah Miller, Jeffrey S. Miller, Manish Patel, M. Felices
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引用次数: 1

Abstract

Background Mesothelioma is a rare, but aggressive cancer that occurs in cells that surround internal organs. Immune check-point inhibitors (ICI) have been approved for the treatment of mesothelioma (nivolumab, ipilimumab and pembrolizumab), but currently approved strategies do not make use of natural killer (NK) cell mediated antibody-dependent cellular cytotoxicity (ADCC) of mesothelioma cells. We hypothesized that combining IL-15 treatment with an anti-PDL1 ICI that drives ADCC will enhance NK cell control of mesothelioma and lead to more robust immune control of the disease. Methods In vitro assays challenged NK cells with three pleural mesothelioma lines, H2373, H2461 and H2596 and four peritoneal mesothelioma lines, ROB, HAY and Flow cytometry was used to assess degranulation and cytokine pro-duction by NK cells co-cultured with mesothelioma cells in short-term assays (5 hours). The tumor cells were treated overnight with IFN g to mimic the inflammatory tumor microenvironment. Natural cytotoxicity was compared with ICI that do not drive ADCC (pembrolizumab), ICI that drive ADCC (avelumab) and IL-15, alone or in combination. Live cell imaging was used to track mesothelioma survival in three dimensional spheroids over 5 days when treated with NK cells and these drugs. NK cell natural cytotoxicity, H2373 H2596 sensitive. resistant
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465自然杀伤细胞聚焦免疫疗法克服间皮瘤实体肿瘤微环境的协同方法
背景间皮瘤是一种罕见但侵袭性的癌症,发生在内脏器官周围的细胞中。免疫检查点抑制剂(ICI)已被批准用于治疗间皮瘤(nivolumab, ipilimumab和pembrolizumab),但目前批准的策略并未利用间皮瘤细胞的自然杀伤(NK)细胞介导的抗体依赖性细胞毒性(ADCC)。我们假设将IL-15治疗与驱动ADCC的抗pdl1 ICI结合将增强NK细胞对间皮瘤的控制,并导致更强大的疾病免疫控制。方法用3种胸膜间皮瘤细胞系H2373、H2461、H2596和4种腹膜间皮瘤细胞系攻击NK细胞,采用ROB、HAY和流式细胞术观察NK细胞与间皮瘤细胞共培养的短期(5小时)脱肉芽和细胞因子的产生。用IFN g处理肿瘤细胞过夜以模拟炎症性肿瘤微环境。将天然细胞毒性与不驱动ADCC(派姆单抗)的ICI、驱动ADCC (avelumab)和IL-15的ICI单独或联合进行比较。使用NK细胞和这些药物治疗后,活细胞成像用于跟踪三维球体中间皮瘤的存活超过5天。NK细胞天然细胞毒性,对H2373 H2596敏感。耐药
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