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伴FLT3突变的急性髓系白血病患者淋巴细胞亚群和细胞因子的表达水平及意义OA北大核心CSTPCD

Expression and significance of lymphocyte subgroups and cytokines in acute myeloid leukemia patients with FLT3 mutations

中文摘要英文摘要

目的:探讨伴FMS样酪氨酸激酶3受体(FMS like tyrosine kinase 3 receptor,FLT3)突变的初诊急性髓系白血病(acute myeloid leukemia,AML)患者外周血淋巴细胞亚群、细胞因子表达水平及其与血细胞计数、突变类型之间的相关性.方法:168例伴FLT3突变的AML患者纳入研究,进一步对FLT3突变类型进行分类,收集患者治疗前外周血淋巴细胞亚群、细胞因子数据及血细胞计数,分析其之间的相关性.结果:与健康对照组相比,伴FLT3突变的AML患者治疗前外周血CD4、白介素6(interleukin 6,IL-6)、IL-10表达水平升高,CD8、CD16+CD56、IL-2、肿瘤坏死因子(tumor necrosis factor,TNF)、干扰素-γ(interferon gamma,IFN-γ)表达水平下降.按白细胞计数分组,CD3、CD4、CD8、CD19、IL-4、IL-10在组间分布差异具有统计学意义(P=0.039、P=0.024、P=0.034、P=0.008、P=0.048、P=0.024);按血小板计数分组,CD19、CD16+CD56在组间分布差异具有统计学意义(P=0.030、P=0.045).按FLT3类型分组,分为FLT3-ITD+、FLT3-TKD+、FLT3-(ITD++TKD+)和FLT3-(ITD-+TKD-)组,CD3、CD8、CD19、IL-10、TNF在4组间分布差异具有统计学意义(P=0.046、P=0.048、P=0.041、P=0.042、P=0.013).结论:伴FLT3突变AML患者的血细胞计数及FLT3突变类型与淋巴细胞亚群和细胞因子的表达水平有关,可能有助于AML危险分层并对AML患者的预后有一定影响.

Objective:To investigate the peripheral blood lymphocyte subsets and cytokine expression levels in newly diagnosed acute myeloid leukemia(AML)patients with FMS like tyrosine kinase 3 receptor(FLT3)mutations,and their correlation with blood cell counts and mutation types.Methods:A total of 168 AML patients with FLT3 mutations were included in the study.The FLT3 mutation types were further classified,and the lymphocyte subsets,cytokines and blood cell count in peripheral blood of patients before treatment were collected to analyze their correlation.Results:Compared with the healthy control group,the expression levels of CD4,interleukin 6(IL-6),and IL-10 in peripheral blood of patients with FLT3 mutations were increased before treatment,while the expression levels of CD8,CD16+CD56,IL-2,tumor necrosis factor(TNF),and interferon gamma(IFN-γ)were decreased.According to leukocyte count,the distributions of CD3,CD4,CD8,CD19,IL-4 and IL-10 were different among the groups(P=0.039,P=0.024,P=0.034,P=0.008,P=0.048,P=0.024).According to platelet count,the distributions of CD19,CD16+CD56 were different among groups(P=0.030,P=0.045).It can be divided into FLT3-ITD+、FLT3-TKD+、FLT3-(ITD++TKD+)and FLT3-(ITD-+TKD-).The distributions of CD3,CD8,CD19,IL-10 and TNF were different among the four groups(P=0.046,P=0.048,P=0.041,P=0.042,P=0.013).Conclusion:The blood cell counts and FLT3 mutation types of AML patients are associated with the expression levels of lymphocyte subsets and cytokines.This may contribute to the risk stratification of AML and have a certain impact on the prognosis of AML patients.

陈洋;谢研研;方玉;周璇;张文静;钱思轩;师锦宁

南京医科大学附属江宁医院血液内科,江苏 南京 211100南京医科大学附属江宁医院输血科,江苏 南京 211100南京医科大学第一附属医院血液内科,江苏南京 210029

临床医学

急性髓系白血病FMS样酪氨酸激酶3受体淋巴细胞亚群细胞因子血细胞计数

acute myeloid leukemiaFMS like tyrosine kinase 3 receptorlymphocyte subgroupscytokinesblood cell count

《南京医科大学学报(自然科学版)》 2024 (004)

499-504 / 6

南京市医学科技发展项目(YKK20200);南京医科大学附属江宁医院免疫细胞转化研究中心(JNYYZXKY292214)

10.7655/NYDXBNSN230565

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