Laboratory of Cell Therapy of Cancer, Institute for Cancer Research and Treatment, Candiolo (Torino), Italy.
J Cancer. 2011;2:363-8. doi: 10.7150/jca.2.363. Epub 2011 Jun 15.
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.
细胞因子诱导的杀伤(CIK)细胞是体外扩增的 T 淋巴细胞的异质性亚群,具有混合的 T-NK 表型,并具有 MHC 非限制性抗肿瘤活性。CIK 细胞的主要功能特性可能解决了目前阻止过继免疫治疗策略成功临床转化的一些主要限制。可以基于外周血单个核细胞相对容易和廉价的体外扩增,获得临床足够数量的免疫效应物,足以进行多次过继输注。MHC 非限制性肿瘤杀伤主要基于 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;已证明其对几种实体瘤和血液恶性肿瘤有效,并且不需要任何 HLA 限制,增加了可能从这种方法中受益的患者数量。最后,CIK 细胞在 HLA 障碍方面的同种异体反应性降低,这对其作为同种异体造血细胞移植后常规供体淋巴细胞输注的替代物具有重要的临床意义,降低了移植物抗宿主病的风险。在本报告中,我们综述了 CIK 细胞的主要功能特性,讨论了提高其抗肿瘤活性和潜在临床应用的最新发现和未来展望。