血清CD4+和NK细胞预测儿童再生障碍性贫血治疗效果的临床意义

吴春灿, 严媚, 海力其古丽·努日丁, 马旭凯, 刘玉

中国当代儿科杂志 ›› 2025, Vol. 27 ›› Issue (6) : 690-695.

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中国当代儿科杂志 ›› 2025, Vol. 27 ›› Issue (6) : 690-695. DOI: 10.7499/j.issn.1008-8830.2410063
论著·临床研究

血清CD4+和NK细胞预测儿童再生障碍性贫血治疗效果的临床意义

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Prognostic value of serum CD4+ and NK cells for the treatment response in children with aplastic anemia

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摘要

目的 探索CD4⁺细胞百分比(CD4⁺%)和NK细胞百分比(NK%)在预测儿童再生障碍性贫血(aplastic anemia, AA)疗效中的临床价值,为精准诊疗提供参考依据。 方法 回顾性研究2019年1月—2024年4月新疆医科大学第一附属医院接受环孢素A治疗的AA患儿临床资料。48例AA患儿为观察组,50例同期体检儿童为对照组。收集两组淋巴细胞亚群数据,分析组间差异及其与疗效的关系。依据血液学反应,将观察组分为有效组18例(HR组,含完全和部分缓解)及无效组30例(NHR组,含未缓解)。 结果 单因素分析显示,观察组的NK%显著低于对照组(P<0.05)。观察组随访3个月。HR组CD4⁺%低于NHR组(P=0.018),NK%高于NHR组(P=0.029)。多因素logistic回归分析显示,高CD4⁺%为疗效差的风险因素(OR=1.062),高NK%为保护因素(OR=0.820)。CD4⁺%与NK%联合预测AA患儿HR的曲线下面积为0.812。 结论 初诊时CD4⁺%水平升高是治疗效果不佳的预测因素,而NK%水平升高则与较好的预后相关。

Abstract

Objective To evaluate the clinical value of CD4⁺ cell percentage (CD4⁺%) and NK cell percentage (NK%) in predicting treatment outcomes in children with aplastic anemia (AA), providing a reference for precise diagnosis and treatment. Methods This retrospective study analyzed the clinical data of AA children treated with cyclosporine A at the First Affiliated Hospital of Xinjiang Medical University from January 2019 to April 2024. The study involved 48 AA children as the observation group and 50 children undergoing medical check-ups during the same period as the control group. Lymphocyte subset data were collected from both groups to analyze differences and their relationship with treatment efficacy. Based on hematological responses, the observation group was divided into an effective group of 18 patients (HR group, including complete and partial remission) and an ineffective group of 30 patients (NHR group, including non-remission). Results Univariate analysis showed that NK% in the observation group was significantly lower than that in the control group (P<0.05). The observation group was followed up for 3 months. The HR group had a lower CD4⁺% than the NHR group (P=0.018) and a higher NK% than the NHR group (P=0.029). Multivariate logistic regression analysis indicated that a high CD4⁺% was a risk factor for poor treatment efficacy (OR=1.062), whereas a high NK% was a protective factor (OR=0.820). The area under the curve for the prediction of HR in pediatric AA by combining CD4⁺% and NK% was 0.812. Conclusions A higher CD4⁺% at diagnosis is a predictor of poor treatment response, whereas a higher NK% is associated with better outcomes.

关键词

再生障碍性贫血 / 血液学反应 / CD4+细胞 / NK细胞 / 儿童

Key words

Aplastic anemia / Hematological response / CD4+ cell / NK cell / Child

引用本文

导出引用
吴春灿, 严媚, 海力其古丽·努日丁, . 血清CD4+和NK细胞预测儿童再生障碍性贫血治疗效果的临床意义[J]. 中国当代儿科杂志. 2025, 27(6): 690-695 https://doi.org/10.7499/j.issn.1008-8830.2410063
Chun-Can WU, Mei YAN, Hailiguli NURIDDIN, et al. Prognostic value of serum CD4+ and NK cells for the treatment response in children with aplastic anemia[J]. Chinese Journal of Contemporary Pediatrics. 2025, 27(6): 690-695 https://doi.org/10.7499/j.issn.1008-8830.2410063

参考文献

1
Vaht K, Göransson M, Carlson K, et al. Incidence and outcome of acquired aplastic anemia: real-world data from patients diagnosed in Sweden from 2000-2011[J]. Haematologica, 2017, 102(10): 1683-1690. PMCID: PMC5622852. DOI: 10.3324/haematol.2017.169862 .
2
陈静. 儿童获得性非重型再生障碍性贫血中西医结合诊疗专家共识[J]. 中国小儿血液与肿瘤杂志, 2021, 26(5): 257-260, 269. DOI: 10.3969/j.issn.1673-5323.2021.05.001 .
3
Young NS, Kaufman DW. The epidemiology of acquired aplastic anemia[J]. Haematologica, 2008, 93(4): 489-492. DOI: 10.3324/haematol.12855 .
4
Alqahtany FS. Idiopathic aplastic anemia in children and adults: diagnosis, treatments, and management: a review[J]. Curr Pharm Biotechnol, 2020, 21(13): 1282-1288. DOI: 10.2174/1389201021666191210141426 .
5
Zhu C, Lian Y, Wang C, et al. Single-cell transcriptomics dissects hematopoietic cell destruction and T-cell engagement in aplastic anemia[J]. Blood, 2021, 138(1): 23-33. PMCID: PMC8349468. DOI: 10.1182/blood.2020008966 .
6
Pagliuca S, Gurnari C, Hercus C, et al. Molecular landscape of immune pressure and escape in aplastic anemia[J]. Leukemia, 2023, 37(1): 202-211. PMCID: PMC10089624. DOI: 10.1038/s41375-022-01723-w .
7
Li JP, Wu KH, Chao WR, et al. Alterations of mesenchymal stem cells on regulating Th17 and Treg differentiation in severe aplastic anemia[J]. Aging (Albany NY), 2023, 15(2): 553-566. PMCID: PMC9925683. DOI: 10.18632/aging.204500 .
8
秦洪成, 管贤敏, 胡艳妮, 等. 单用环孢素治疗儿童获得性再生障碍性贫血的疗效及影响因素分析[J]. 中国实验血液学杂志, 2024, 32(3): 841-846. DOI: 10.19746/j.cnki.issn1009-2137.2024.03.029 .
9
孙高源, 田新, 毛晓燕, 等. 单用环孢素A与环孢素A联合ATG治疗儿童重型再生障碍性贫血的临床疗效比较[J]. 中国小儿血液与肿瘤杂志, 2021, 26(2): 98-101. DOI: 10.3969/j.issn.1673-5323.2021.02.008 .
10
国家卫生健康委办公厅. 儿童再生障碍性贫血诊疗规范(2019年版)[J]. 全科医学临床与教育, 2019, 17(11): 965-969. DOI: 10.13558/j.cnki.issn1672-3686.2019.011.002 .
11
朱琳超, 孙菊琴, 姚轶敏. 红细胞输注疗效和铁过载对再生障碍性贫血患者T淋巴细胞亚群的影响[J]. 浙江医学, 2022, 44(11): 1165-1168. DOI: 10.12056/j.issn.1006-2785.2022.44.11.2021-3790 .
12
Furlong E, Carter T. Aplastic anaemia: Current concepts in diagnosis and management[J]. J Paediatr Child Health, 2020, 56(7): 1023-1028. DOI: 10.1111/jpc.14996 .
13
Ritz C, Meng W, Stanley NL, et al. Postvaccination graft dysfunction/aplastic anemia relapse with massive clonal expansion of autologous CD8+ lymphocytes[J]. Blood Adv, 2020, 4(7): 1378-1382. PMCID: PMC7160279. DOI: 10.1182/bloodadvances.2019000853 .
14
吴鸿飞, 王世充, 黄金波, 等. 淋巴细胞亚群在鉴别低增生性骨髓增生异常综合征和再生障碍性贫血中的价值[J]. 中国实验血液学杂志, 2023, 31(4): 1125-1132. DOI: 10.19746/j.cnki.issn1009-2137.2023.04.030 .
15
Merli P, Quintarelli C, Strocchio L, et al. The role of interferon-gamma and its signaling pathway in pediatric hematological disorders[J]. Pediatr Blood Cancer, 2021, 68(4): e28900. DOI: 10.1002/pbc.28900 .
16
Li H, Fu L, Yang B, et al. Cyclosporine monotherapy in pediatric patients with non-severe aplastic anemia: a retrospective analysis[J]. Front Med (Lausanne), 2022, 9: 805197. PMCID: PMC8948483. DOI: 10.3389/fmed.2022.805197 .
17
Sharma V, Kumar P, Kumar R, et al. Interferon-gamma and perforin-positive T cells in acquired aplastic anemia: implication in therapeutic response[J]. Clin Exp Immunol, 2022, 207(3): 272-278. PMCID: PMC9113177. DOI: 10.1093/cei/uxab006 .
18
Li Y, Ding S, Liu C, et al. Abnormalities of quantities and functions of CD56bright natural killer cells in non-severe aplastic Anemia[J]. Hematology, 2019, 24(1): 405-412. DOI: 10.1080/16078454.2019.1590963 .
19
Liu H, Zhang T, Chen Y, et al. Proteomics analysis reveals alterations of NK cells in patients with severe aplastic anemia[J]. Int J Lab Hematol, 2020, 42(3): 308-315. DOI: 10.1111/ijlh.13175 .
20
Peng H, Tian Z. NK cells in liver homeostasis and viral hepatitis[J]. Sci China Life Sci, 2018, 61(12): 1477-1485. DOI: 10.1007/s11427-018-9407-2 .
21
Shemer A, Scheyltjens I, Frumer GR, et al. Interleukin-10 prevents pathological microglia hyperactivation following peripheral endotoxin challenge[J]. Immunity, 2020, 53(5): 1033-1049.e7. DOI: 10.1016/j.immuni.2020.09.018 .
22
Veh J, Ludwig C, Schrezenmeier H, et al. Regulatory B cells-immunopathological and prognostic potential in humans[J]. Cells, 2024, 13(4): 357. PMCID: PMC10886933. DOI: 10.3390/cells13040357 .

作者贡献声明

吴春灿、马旭凯负责研究实施、论文撰写;吴春灿、海力其古丽·努日丁负责数据整理、统计分析;严媚、刘玉负责研究指导、论文修改、经费支持。

基金

“天山英才”医药卫生高层次人才培养计划(TSYC202301A002)
“青年科研起航”专项基金(2023YFY-QKQN-09)
免疫性疾病研究槐杞黄专项基金(CXPJJH122003-55)
儿童重大疾病基础研究、专病队列研究以及预警模型构建研究(2024B03038)

编委: 张辉

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