Konjević Gordana, Vuletić Ana, Mirjačić Martinović Katarina
Department of Experimental Oncology, Institute of Oncology and Radiology of Serbia, 14 Pasterova, Belgrade, 11000, Serbia.
Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Immunol Res. 2016 Feb;64(1):25-35. doi: 10.1007/s12026-015-8695-4.
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-α, 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.
众多新发现的激活型和抑制型自然杀伤(NK)细胞受体及其与靶肿瘤细胞上同源配体的结合,调节着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。全身应用以及用于体外激活和扩增NK细胞的细胞因子,如干扰素-α(IFN-α)、白细胞介素-2(IL-2)、白细胞介素-12(IL-12)、白细胞介素-15(IL-15)和白细胞介素-18(IL-18),通过增加NK细胞激活受体的表达和诱导细胞毒性效应分子,提高了NK细胞的抗肿瘤活性。此外,人们已经认识到,经典和新型药物制剂可上调肿瘤细胞上激活受体的同源配体,并提供更好的NK细胞抗肿瘤反应。在供体-受体杀伤细胞免疫球蛋白样受体(KIR)/人类白细胞抗原(HLA)不匹配的情况下,癌症中的一些其他免疫治疗方法也在不断发展,目的是增强异基因造血干细胞移植中的NK细胞活性,从而产生有益的移植物抗肿瘤效应。因此,需要更好地了解NK细胞激活和抑制受体生物学,以协助开发有效操纵NK细胞的新方法,并为癌症患者创建基于NK细胞的有效免疫疗法。