Davis Carter T, Rizzieri David
Pharmaceuticals (Basel). 2015 May 25;8(2):250-6. doi: 10.3390/ph8020250.
Natural Killer (NK) cells are lymphoid cells that exhibit an innate response against virus-infected cells. These cells are also capable of mounting an immune response against tumor cells after education through major histocompatibility complex (MHC) class I molecules. NK cell regulation is mediated through IFN-gamma and IL-15, important cytokines which can drive NK cell expansion in vivo. Previous studies have shown effective infusion of allogeneic NK cells after lymphodepleting regimens with induction of remission of poor prognosis acute myeloid leukemia (AML). Challenges remain in the expansion of these NK cells once infused and in their education to recognize tumor targets. A principal mechanism of tumor recognition is through KIR mismatch in cells lacking self MHC I molecules. Activating KIRs exist, though their ligands are unknown at this time. Impacting NK cell expansion and education in vivo has been challenging, and thus far clinical applications of NK cells have shown promise in helping to maintain remission in humans, though this remission has not been maintained. Future efforts to utilize NK cells clinically are focusing on developing more consistency in successful expansion of NK cell and educating them to recognize their tumor targets. Additional efforts to utilize novel antibody-based therapy to engage NK cells to their tumor targets are also in development.
自然杀伤(NK)细胞是一类淋巴细胞,对病毒感染细胞表现出先天性免疫反应。这些细胞在通过主要组织相容性复合体(MHC)I类分子进行“教育”后,也能够对肿瘤细胞发起免疫反应。NK细胞的调节是通过γ干扰素和白细胞介素-15介导的,这两种重要的细胞因子可在体内驱动NK细胞扩增。先前的研究表明,在采用淋巴细胞清除方案后有效输注异基因NK细胞,可诱导预后不良的急性髓系白血病(AML)缓解。然而,这些NK细胞一旦输注后在扩增以及“教育”它们识别肿瘤靶点方面仍存在挑战。肿瘤识别的主要机制是通过缺乏自身MHC I类分子的细胞中的杀伤细胞免疫球蛋白样受体(KIR)错配。虽然目前尚不清楚其配体,但存在激活型KIR。在体内影响NK细胞的扩增和“教育”一直具有挑战性,迄今为止,NK细胞的临床应用已显示出有助于维持人类缓解的前景,尽管这种缓解尚未持续。未来NK细胞临床应用的努力方向集中在更一致地成功扩增NK细胞并“教育”它们识别肿瘤靶点。利用新型抗体疗法使NK细胞作用于肿瘤靶点的其他努力也在开展中。