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Cytokine Induced Killer Cells as Promising Immunotherapy for Solid Tumors

机译:细胞因子诱导的杀伤细胞有望成为实体瘤的免疫疗法

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摘要

Cytokine-induced killer (CIK) cells are a heterogeneous subset of ex-vivo expanded T lymphocytes which present a mixed T-NK phenotype and are endowed with a MHC-unrestricted antitumor activity. The main functional properties of CIK cells may address some of the main limitations that are currently preventing the successful clinical translation of adoptive immunotherapy strategies. Clinically adequate quantities of immune effectors, sufficient for multiple adoptive infusions, may be obtained based on their relatively easy and inexpensive ex-vivo expansion starting from peripheral blood mononuclear cells. The MHC-unrestricted tumor-killing is mainly based on the interaction between NKG2D molecules on CIK cells and MIC A/B or ULBPs molecules on tumor cells; it has been proved effective against several solid and hematological malignancies and does not require any HLA-restriction increasing the number of patients that might potentially benefit from such approach. Finally, CIK cells present a reduced alloreactivity across HLA-barriers with important clinical implications for their potential use as alternative to conventional Donor Lymphocyte Infusions after allogeneic hemopoietic cell transplant with a reduced risk of GVHD. In the present report we review the main functional characteristics of CIK cells discussing recent findings and future perspectives to improve their antitumor activity and potential clinical applications.
机译:细胞因子诱导的杀伤细胞(CIK)是离体扩增T淋巴细胞的异质子集,具有混合的T-NK表型,并具有MHC不受限制的抗肿瘤活性。 CIK细胞的主要功能特性可能解决了一些主要限制因素,这些限制因素目前正在阻止过继免疫治疗策略的成功临床翻译。基于它们从外周血单核细胞开始的相对容易和廉价的离体扩增,可以获得足以进行多次过继输注的临床上足够量的免疫效应物。 MHC不受限制的肿瘤杀伤作用主要基于CIK细胞上的NKG2D分子与肿瘤细胞上的MIC A / B或ULBPs分子之间的相互作用。它已被证明对多种实体和血液恶性肿瘤有效,并且不需要任何HLA限制,而增加了可能从这种方法中受益的患者数量。最后,CIK细胞跨HLA屏障的同种异体反应性降低,对于其在异基因造血细胞移植后替代常规供体淋巴细胞输注的潜在用途具有潜在的GVHD风险具有重要的临床意义。在本报告中,我们回顾了CIK细胞的主要功能特征,讨论了最近的发现和未来观点,以改善其抗肿瘤活性和潜在的临床应用。

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