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Immunotherapeutic Applications of NK Cells

机译:NK细胞的免疫治疗应用

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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.
机译:天然杀伤(NK)细胞是淋巴样细胞,对病毒感染的细胞表现出先天反应。这些细胞还可以通过主要的组织相容性复合体(MHC)I类分子,对肿瘤细胞进行免疫反应。 NK细胞调节是通过IFN-γ和IL-15介导的,IFN-γ和IL-15是重要的细胞因子,可在体内驱动NK细胞扩增。先前的研究表明,淋巴切除方案后可有效输注同种异体NK细胞,并诱导不良预后的急性髓细胞性白血病(AML)缓解。一旦注入这些NK细胞并对其进行识别肿瘤靶标的教育,挑战仍然存在。肿瘤识别的主要机制是通过缺乏自身MHC I分子的细胞中的KIR错配。存在活化的KIR,尽管此时它们的配体尚不清楚。影响NK细胞在体内的扩增和教育一直是挑战性的,迄今为止,NK细胞的临床应用已显示出有望帮助维持人类的缓解,尽管这种缓解尚未得到维持。未来临床上利用NK细胞的努力主要集中在发展成功的NK细胞扩增并培养其识别肿瘤靶标的一致性方面。利用基于抗体的新型疗法使NK细胞与其肿瘤靶标结合的其他努力也在开发中。

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