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Combining Antiangiogenic Therapy with Adoptive Cell Immunotherapy Exerts Better Antitumor Effects in Non-Small Cell Lung Cancer Models

机译:抗血管生成疗法与过继细胞免疫疗法的结合在非小细胞肺癌模型中具有更好的抗肿瘤作用

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摘要

IntroductionCytokine-induced killer cells (CIK cells) are a heterogeneous subset of ex-vivo expanded T lymphocytes which are characterized with a MHC-unrestricted tumor-killing activity and a mixed T-NK phenotype. Adoptive CIK cells transfer, one of the adoptive immunotherapy represents a promising nontoxic anticancer therapy. However, in clinical studies, the therapeutic activity of adoptive CIK cells transfer is not as efficient as anticipated. Possible explanations are that abnormal tumor vasculature and hypoxic tumor microenvironment could impede the infiltration and efficacy of lymphocytes. We hypothesized that antiangiogenesis therapy could improve the antitumor activity of CIK cells by normalizing tumor vasculature and modulating hypoxic tumor microenvironment.
机译:简介细胞因子诱导的杀伤细胞(CIK细胞)是离体扩增T淋巴细胞的异质子集,其特征是MHC不受限制的肿瘤杀伤活性和混合的T-NK表型。过继CIK细胞转移是过继免疫疗法之一,代表了一种有前途的无毒抗癌疗法。但是,在临床研究中,过继CIK细胞转移的治疗活性不如预期的有效。可能的解释是异常的肿瘤脉管系统和缺氧的肿瘤微环境可能会阻碍淋巴细胞的浸润和效力。我们假设抗血管生成疗法可以通过使肿瘤脉管正常化和调节缺氧肿瘤微环境来改善CIK细胞的抗肿瘤活性。

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