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自然杀伤细胞激活受体基因变异对急性髓系白血病免疫治疗受体表达和结果的影响。

Impact of NK Cell Activating Receptor Gene Variants on Receptor Expression and Outcome of Immunotherapy in Acute Myeloid Leukemia.

机构信息

Tumor Immunology (TIMM) Laboratory at Sahlgrenska Center for Cancer Research, University of Gothenburg, Gothenburg, Sweden.

Department of Medical Biochemistry and Cell Biology, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.

出版信息

Front Immunol. 2021 Dec 9;12:796072. doi: 10.3389/fimmu.2021.796072. eCollection 2021.

Abstract

Natural killer cells are important effector cells in the immune response against myeloid malignancies. Previous studies show that the expression of activating NK cell receptors is pivotal for efficient recognition of blasts from patients with acute myeloid leukemia (AML) and that high expression levels impact favorably on patient survival. This study investigated the potential impact of activating receptor gene variants on NK cell receptor expression and survival in a cohort of AML patients receiving relapse-preventive immunotherapy with histamine dihydrochloride and low-dose IL-2 (HDC/IL-2). Patients harboring the G allele of rs1049174 in the gene encoding NKG2D showed high expression of NKG2D by CD56 NK cells and a favorable clinical outcome in terms of overall survival. For DNAM-1, high therapy-induced receptor expression entailed improved survival, while patients with high DNAM-1 expression before immunotherapy associated with unfavorable clinical outcome. The previously reported SNPs in encoding NKp30, which purportedly influence mRNA splicing into isoforms with discrete functions, did not affect outcome in this study. Our results imply that variations in genes encoding activating NK cell receptors determine receptor expression and clinical outcome in AML immunotherapy.

摘要

自然杀伤细胞是免疫反应中对抗髓系恶性肿瘤的重要效应细胞。先前的研究表明,激活 NK 细胞受体的表达对于有效识别急性髓细胞白血病 (AML) 患者的白血病细胞至关重要,并且高表达水平对患者的生存有积极影响。本研究调查了在接受盐酸组胺和低剂量白细胞介素-2 (HDC/IL-2) 预防复发免疫治疗的 AML 患者队列中,激活受体基因变异对 NK 细胞受体表达和生存的潜在影响。在编码 NKG2D 的基因中 rs1049174 位点携带 G 等位基因的患者,其 CD56 NK 细胞表达高水平的 NKG2D,并在总体生存方面具有良好的临床结局。对于 DNAM-1,高治疗诱导的受体表达意味着生存改善,而在免疫治疗前具有高 DNAM-1 表达的患者与不良的临床结局相关。本研究中未发现先前报道的编码 NKp30 的基因中的 SNPs 影响 mRNA 剪接成具有不同功能的异构体,从而影响结果。我们的研究结果表明,编码激活 NK 细胞受体的基因变异决定了 AML 免疫治疗中的受体表达和临床结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c9/8695486/4a32bbbdf418/fimmu-12-796072-g001.jpg

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