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Clinical Application of iNKT Cell-mediated Anti-tumor Activity Against Lung Cancer and Head and Neck Cancer

机译:iNKT细胞介导的抗肺癌和头颈癌抗肿瘤活性的临床应用

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摘要

Invariant natural killer T (iNKT) cells produce copious amounts of cytokines in response to T-cell receptor (TCR) stimulation by recognizing antigens such as α-galactosylceramide (α-GalCer) presented on CD1d; thus, orchestrating other immune cells to fight against pathogen infection and tumors. Because of their ability to induce strong anti-tumor responses and the convenience of their invariant TCR activated by a synthetic ligand, α-GalCer, iNKT cells have been intensively studied for application in immunotherapeutic approaches to treat cancer patients in the clinic. Here, we summarize the clinical trials of iNKT cell based immunotherapy for non-small cell lung cancer, and head and neck cancer. Although solid tumors are thought to be refractory to immunotherapeutic approaches, our clinical trials showed that the intravenous injection of α-GalCer-pulsed antigen presenting cells (APCs) activated endogenous iNKT cells and iNKT cell dependent responses. Moreover, an increase in the number of IFN-γ producing cells in PBMCs was associated with prolonged survival. The marked infiltration of iNKT cells and the accumulation of conventional T cells in the tumor microenvironment were also observed after the administration of α-GalCer-pulsed APCs and/or ex vivo activated iNKT cells. In cases of advanced head and neck squamous cell carcinoma, the increased accumulation of iNKT cells in the tumor microenvironment was correlated with objective clinical responses. We will also discuss potential combination therapies of iNKT cell based immunotherapy to achieve enhanced anti-tumor activity and provide better treatment options for these patients.
机译:不变的自然杀伤性T细胞(iNKT)通过识别CD1d上存在的抗原,例如α-半乳糖基神经酰胺(α-GalCer),来响应T细胞受体(TCR)刺激而产生大量的细胞因子。因此,协调其他免疫细胞以抵抗病原体感染和肿瘤。由于iNKT细胞具有诱导强烈的抗肿瘤反应的能力以及被合成配体激活的不变TCR的便利性,因此在临床上对iNKT细胞进行了深入研究,以用于免疫治疗方法来治疗癌症患者。在这里,我们总结了基于iNKT细胞的免疫疗法用于非小细胞肺癌和头颈癌的临床试验。尽管人们认为实体瘤对免疫治疗方法无效,但我们的临床试验表明,静脉注射α-GalCer脉冲抗原呈递细胞(APC)可激活内源性iNKT细胞和iNKT细胞依赖性反应。此外,PBMC中产生IFN-γ的细胞数量增加与存活时间延长有关。在施用α-GalCer脉冲的APC和/或离体激活的iNKT细胞后,还观察到了iNKT细胞的显着浸润和常规T细胞在肿瘤微环境中的积累。对于晚期头颈部鳞状细胞癌,iNKT细胞在肿瘤微环境中积累的增加与客观临床反应相关。我们还将讨论基于iNKT细胞的免疫疗法的潜在联合疗法,以增强抗肿瘤活性,并为这些患者提供更好的治疗选择。

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