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鉴定 CD16low CD56low CD38posNK 细胞为多发性骨髓瘤患者的关键亚群

英文原题:Identification of the CD16low CD56low CD38pos Natural Killer Cell as a Key Subset in Patients with Multiple Myeloma.

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Identification of the CD16low CD56low CD38pos Natural Killer Cell as a Key Subset in Patients with Multiple Myeloma.

PubMed 2022/12/01(内容时间) Iran J Immunol Q4 · IF 1.1(JCR 2025)

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研究概要

我们的数据提示,CD16low CD56low CD38pos NK 细胞可能反映为一种效应细胞群,在 MM 患者中具有潜在的治疗靶点。这组细胞未来可能可用于 MM 的过继性免疫治疗。

研究思路结论见上方概要

自然杀伤(NK)细胞被归类为先天免疫细胞,无需抗原致敏即可直接识别并杀伤肿瘤细胞。近年来,基于NK细胞的过继免疫治疗血液恶性肿瘤受到更多关注。

分析多发性骨髓瘤(MM)患者外周血和骨髓(BM)中不同的NK细胞亚群。

使用流式细胞术,我们分析了:(i) 不同疾病阶段MM患者BM中不同NK细胞亚群的分布(即CD16low CD56low、CD16pos CD56high、CD16neg CD56high、CD16high CD56low、CD16neg CD56low、CD16low CD56low CD38pos)。(ii) NKG2D、DNAM-1和NKp30的表达,以及(iii) CD16low CD56low CD38pos和CD16low CD56low CD38neg NK细胞亚群中CD107a的表达。

CD16low CD56low CD38pos是MM患者CR期BM中的主要亚群,NKp30表达降低。与CD16low CD56low CD38neg细胞相比,CD16low CD56low CD38pos亚群显示出更高比例的CD107a表达。体外实验表明,CD16low CD56low CD38pos NK细胞亚群比CD16low CD56low CD38neg NK细胞具有更强的细胞毒性。

展开英文摘要原文

Natural killer (NK) cells are classified as innate immune cells which can directly recognize and kill tumor cells without antigen sensitization. NK cell-based adoptive immunotherapy for blood malignancies has attracted more attention in recent years.

To analyze different NK cell subsets in the peripheral blood and bone marrow (BM) of patients with multiple myeloma (MM).

Using flow cytometry we analyzed: (i) the distribution of distinct NK cell subpopulations (i.e. CD16low CD56low, CD16pos CD56high, CD16neg CD56high, CD16high CD56low, CD16neg CD56low, CD16low CD56low CD38pos) in the BM from MM patients at distinct disease stages. (ii) the expression of NKG2D, DNAM-1 and NKp30, and (iii) the expression of CD107a in CD16low CD56low CD38pos and CD16low CD56low CD38neg NK cells subsets.

CD16low CD56low CD38pos was the dominant subset in BM from patients with MM at the CR stage with a decreased expression of NKp30. CD16low CD56low CD38pos subset showed a higher proportion of CD107a expression compared to CD16low CD56low CD38neg cells. In vitro experiments indicated that the CD16low CD56low CD38pos NK cell subset possesses more cytotoxicity than CD16low CD56low CD38neg NK cells.

Our data suggest that CD16low CD56low CD38pos NK cells may reflect as an effector population with the potential therapeutic target in patients with MM. This group of cells may be useful for adoptive immunotherapy in MM in the future.

论文信息

作者
Chen T、Yu Z
单位
The First Clinical Medical College of Nanjing University of Chinese Medicine, 138 Xianlin Road, Nanjing, 210029, ChinaChina
期刊
Iranian journal of immunology : IJI2022 Dec
原文标识
PubMed 36585877 · DOI 10.22034/IJI.2022.93965.2269