Nagai Kei
Department of Nephrology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Ren Replace Ther. 2021;7(1):8. doi: 10.1186/s41100-021-00324-0. Epub 2021 Feb 12.
Natural killer (NK) cells are known to play an important role in defense against infection and tumors. Although there is no clear consensus, most studies have shown that the number and cytotoxicity of NK cells decreases in end-stage kidney disease (ESKD) patients undergoing hemodialysis. Uremic patients chronically suffer from oxidative stress, which could be responsible for downregulation of the activating receptors on NK cells and modulation of ligand expression for activating receptors. Theoretically, the reduced number of NK cells and decreased function might increase susceptibility to viral infections and cancer development in patients with ESKD. There is emerging evidence that NK cell numbers may be an outcome predictor in renal transplantation; however, the clinical significance of NK cell dysfunction in dialysis patients requires clarification. In this review, I describe NK cell number, cytotoxic activity, and activating mechanisms in the context of uremia and oxidative stress, which is anticipated to assist in elucidating the mechanisms underlying immunodeficiency in dialysis patients.
自然杀伤(NK)细胞在抵御感染和肿瘤方面发挥着重要作用。尽管尚无明确共识,但大多数研究表明,接受血液透析的终末期肾病(ESKD)患者的NK细胞数量和细胞毒性会降低。尿毒症患者长期遭受氧化应激,这可能是NK细胞上激活受体下调以及激活受体配体表达调节的原因。理论上,NK细胞数量减少和功能下降可能会增加ESKD患者对病毒感染和癌症发展的易感性。有新证据表明,NK细胞数量可能是肾移植的预后预测指标;然而,透析患者中NK细胞功能障碍的临床意义尚需阐明。在这篇综述中,我将在尿毒症和氧化应激的背景下描述NK细胞数量、细胞毒性活性及激活机制,预计这将有助于阐明透析患者免疫缺陷的潜在机制。