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Natural killer cell receptors: alterations and therapeutic targeting in malignancies

机译:天然杀伤细胞受体:恶性肿瘤的改变和治疗靶点

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摘要

Numerous newly identified activating and inhibitory NK cell receptors and their engagement by cognate ligands on target tumor cells regulate NK cell antitumor activity. Alterations in NK cell receptor expression and signaling underlie diminished cytotoxic NK cell function. Cytokines, IFN-alpha, IL-2, IL-12, IL-15 and IL-18, applied systemically and for ex vivo activation and expansion of NK cells have improved NK cell antitumor activity by increasing the expression of NK cell activating receptors and by inducing cytotoxic effector molecules. Moreover, it has been recognized that classical and novel pharmacological agents upregulate cognate ligands for activating receptors on tumor cells and provide better NK cell antitumor response. Some other immunotherapeutic approaches in cancer in the setting of donor-recipient KIR/HLA mismatch have evolved with the aim to potentiate NK cell activity in allogeneic hematopoietic stem cell transplantation that lead to beneficial graft vs. tumor effect. Therefore, better understanding of NK cell activating and inhibitory receptor biology is needed to assist in developing novel approaches to effectively manipulate NK cells and create effective NK cell-based immunotherapy for treatment of cancer patients.
机译:新近鉴定出的许多激活和抑制性NK细胞受体及其与目标肿瘤细胞上同源配体的结合调节了NK细胞的抗肿瘤活性。 NK细胞受体表达和信号传导的改变是细胞毒性NK细胞功能减弱的基础。全身应用和用于离体激活和扩增NK细胞的细胞因子IFN-α,IL-2,IL-12,IL-15和IL-18通过增加NK细胞激活受体的表达而改善了NK细胞的抗肿瘤活性。通过诱导细胞毒性效应分子。此外,已经认识到经典和新型药理学药物上调同源配体以激活肿瘤细胞上的受体并提供更好的NK细胞抗肿瘤应答。为了增强同种异体造血干细胞移植中NK细胞的活性,从而导致移植物对肿瘤的有益作用,在供体-受体KIR / HLA错配的情况下,癌症中的其他一些免疫治疗方法也在不断发展。因此,需要对NK细胞活化和抑制性受体生物学有更好的了解,以协助开发新颖的方法来有效地操纵NK细胞并创建有效的基于NK细胞的免疫疗法来治疗癌症患者。

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