临床研究

中性粒细胞胞外诱捕网标记物游离DNA与儿童肺炎支原体肺炎的关系

  • 杨雪妮 ,
  • 胡宜航 ,
  • 纪敏 ,
  • 李玉勤 ,
  • 卢红艳 ,
  • 常明
展开
  • 江苏大学附属医院儿科 (江苏 镇江 212001 )

收稿日期: 2025-09-28

  网络出版日期: 2025-12-18

基金资助

江苏省卫生健康委科研项目(M2022043);镇江市儿童呼吸疾病临床医学重点实验室项目(SS2023012)

Association between neutrophic extracellular trap marker (cell⁃free DNA) and mycoplasma pneumoniae pneumonia in children

  • Xueni YANG ,
  • Yihang HU ,
  • Min JI ,
  • Yuqin LI ,
  • Hongyan LU ,
  • Ming. CHANG
Expand
  • Department of Pediatrics,Jiangsu University Affiliated Hospital,Zhenjiang 212001,Jiangsu,China

Received date: 2025-09-28

  Online published: 2025-12-18

摘要

目的 分析中性粒细胞胞外诱捕网(NETs)标记物游离DNA(cf-DNA)在肺炎支原体肺炎(MPP)患儿体内的表达水平,探讨cf-DNA/NETs对MPP患儿病情严重程度的预测效能。 方法 前瞻性选取115例MPP患儿作为MPP组,根据病情严重程度,将MPP组分为轻症组(n = 75)和重症组(n = 40)。同期随机选取50例健康体检儿童作为对照组。检测MPP组及对照组血清cf-DNA水平及MPP组C反应蛋白(CRP)、D-二聚体、乳酸脱氢酶(LDH)、白介素-6(IL-6)、γ干扰素(IFN-γ)及肿瘤坏死因子-α(TNF-α)水平,比较各组血清cf-DNA及相关炎症因子的水平差异,并分析血清cf-DNA在评估MPP病情严重程度中的作用。 结果 MPP组患儿血清cf-DNA水平较对照组明显升高,且在重症组升高更显著(P < 0.05)。重症组CRP、D-二聚体、LDH、IL-6、IFN-γ及TNF-α水平均高于轻症组(P < 0.05)。多因素logistic回归分析发现血清cf-DNA、CRP及IL-6水平升高与MPP病情严重程度密切相关(P < 0.05)。受试者操作特征曲线分析结果显示血清cf-DNA、CRP及IL-6三者联合预测重症MPP的曲线下面积为0.981,高于各指标单独预测(P < 0.05)。 结论 血清cf-DNA/NETs与MPP患儿病情严重程度密切相关,cf-DNA、CRP及IL-6三者联合检测更有利于判断MPP患儿的病情严重程度。

本文引用格式

杨雪妮 , 胡宜航 , 纪敏 , 李玉勤 , 卢红艳 , 常明 . 中性粒细胞胞外诱捕网标记物游离DNA与儿童肺炎支原体肺炎的关系[J]. 实用医学杂志, 2025 , 41(23) : 3711 -3716 . DOI: 10.3969/j.issn.1006-5725.2025.23.012

Abstract

Objective The aim of this study is to analyze the expression level of cell-free DNA (cf-DNA), a biomarker of neutrophil extracellular traps (NETs), in children with Mycoplasma pneumoniae pneumonia (MPP), and to explore the predictive efficacy of cf-DNA (as a marker of NETs) for the severity of MPP in these children. Methods A total of 115 children with MPP were prospectively selected as the MPP group. Based on the disease severity, the MPP group was categorized into the mild group (n = 75) and the severe group (n = 40). During the same period, 50 healthy children undergoing physical examinations were selected as the control group. The levels of serum cf-DNA in the MPP group and the control group, as well as the levels of C-reactive protein (CRP), D-dimer, lactate dehydrogenase (LDH), interleukin-6 (IL-6), interferon-γ (IFN-γ), and tumor necrosis factor-α (TNF-α) in the MPP group were detected. The differences in the levels of serum cf-DNA and related inflammatory factors among the groups were compared, and the role of serum cf-DNA in evaluating the severity of MPP was analyzed. Results The level of serum cf-DNA in children of the MPP group was notably higher than that in the control group, with a more significant elevation observed in the severe group (P < 0.05). The levels of CRP, D-dimer, LDH, IL-6, IFN-γ, and TNF-α were all higher in the severe group than in the mild group (P < 0.05). Multivariate logistic regression analysis showed that the increased levels of serum cf-DNA, CRP, and IL-6 were closely related to the severity of MPP (P < 0.05). The results of receiver operating characteristic (ROC) curve analysis showed that the area under the curve (AUC) of the combination of serum cf-DNA, CRP, and IL-6 for predicting severe MPP was 0.981, which was higher than that of each index alone (P < 0.05). Conclusions Serum cf-DNA (as a marker of NETs) is closely related to the severity of MPP in children. The combined detection of cf-DNA, CRP, and IL-6 is more beneficial for assessing the severity of MPP in children.

参考文献

[1] 刘金荣, 赵成松, 赵顺英. 《儿童社区获得性肺炎诊疗规范(2019年版)》解读[J]. 中国实用儿科杂志, 2020, 35(3): 185-187.
[2] ROH E J, SHIM J Y, CHUNG E H. Epidemiology and surveillance implications of community-acquired pneumonia in children[J]. Clin Exp Pediatr, 2022, 65(12): 563-573. doi:10.3345/cep.2022.00374
[3] 赵顺英, 钱素云, 陈志敏, 等. 儿童肺炎支原体肺炎诊疗指南(2023年版)[J]. 新发传染病电子杂志, 2024, 9(1): 73-79.
[4] BIAN C, LI S, HUO S, et al. Association of atopy with disease severity in children with Mycoplasma pneumoniae pneumonia[J]. Front Pediatr, 2023, 11: 1281479. doi:10.3389/fped.2023.1281479
[5] LEE W, KO S Y, AKASAKA H, et al. Neutrophil extracellular traps promote pre-metastatic niche formation in the omentum by expanding innate-like B cells that express IL-10[J]. Cancer Cell, 2025, 43(1): 69-85. doi:10.1016/j.ccell.2024.12.004
[6] VARJú I, TANKA-SALAMON A, KOLEV K. Neutrophil Extracellular Traps: At the Interface of Thrombosis and Comorbidities[J]. Semin Thromb Hemost, 2025, 51(7): 724-735. doi:10.1055/a-2548-0805
[7] HUANG S U-S, O’SULLIVAN K M. The Expanding Role of Extracellular Traps in Inflammation and Autoimmunity: The New Players in Casting Dark Webs[J]. Int J Mol Sci, 2022, 23(7): 3793. doi:10.3390/ijms23073793
[8] GIERLIKOWSKA B, STACHURA A, GIERLIKOWSKI W, et al. The Impact of Cytokines on Neutrophils’ Phagocytosis and NET Formation during Sepsis—A Review[J]. Int J Mol Sci, 2022, 23(9): 5076. doi:10.3390/ijms23095076
[9] MEYER SAUTEUR P M. Childhood community-acquired pneumonia[J]. Eur J Pediatr, 2024, 183(3): 1129-1136. doi:10.1007/s00431-023-05366-6
[10] KANG D, YUN K W, LEE T, et al. Treatment modalities for fever duration in children with Mycoplasma pneumoniae pneumonia[J]. Sci Rep, 2025, 15(1): 14860. doi:10.1038/s41598-025-99537-0
[11] CHOO S, KIM S-H, LEE E. Clinical significance of Mycoplasma pneumoniae specific IgM titer in children hospitalized with Mycoplasma pneumoniae pneumonia[J]. BMC Infect Dis, 2022, 22(1): 470. doi:10.1186/s12879-022-07456-6
[12] ZHANG X, SUN R, HOU J, et al. Clinical characteristics and risk factors of pulmonary embolism with Mycoplasma pneumoniae pneumonia in children[J]. Sci Rep, 2024, 14(1): 24043. doi:10.1038/s41598-024-74302-x
[13] XU M, LI Y, SHI Y, et al. Molecular epidemiology of Mycoplasma pneumoniae pneumonia in children, Wuhan, 2020–2022[J]. BMC Microbiol, 2024, 24(1): 23. doi:10.1186/s12866-024-03180-0
[14] 彭力, 钟礼立, 林琳, 等. 黏蛋白MUC5AC在肺炎支原体肺炎患儿气道中的表达及临床意义[J]. 实用医学杂志, 2023, 39(20): 2618-2622.
[15] FANG C, MAO Y, JIANG M, et al. Pediatric Critical Illness Score, Clinical Characteristics and Comprehensive Treatment of Children with Severe Mycoplasma Pneumoniae Pneumonia[J]. Front Surg, 2022, 9: 897550. doi:10.3389/fsurg.2022.897550
[16] ZHANG H, LI X, WANG J, et al. Baicalin relieves Mycoplasma pneumoniae infection?induced lung injury through regulating microRNA?221 to inhibit the TLR4/NF?κB signaling pathway[J]. Mol Med Rep, 2021, 24(2): 571. doi:10.3892/mmr.2021.12210
[17] HU S, YE J, GUO Q, et al. Serum lactate dehydrogenase is associated with impaired lung function: NHANES 2011–2012[J]. PLoS One, 2023, 18(2): e0281203. doi:10.1371/journal.pone.0281203
[18] 肖志清, 吴雪, 邱蕊, 等. 儿童难治性肺炎支原体肺炎多因子预测模型构建与验证[J]. 实用医学杂志, 2025, 41(13): 2004-2010.
[19] LUO H, HE J, QIN L, et al. Mycoplasma pneumoniae lipids license TLR-4 for activation of NLRP3 inflammasome and autophagy to evoke a proinflammatory response[J]. Clin Exp Immunol, 2021, 203(1): 66-79. doi:10.1111/cei.13510
[20] MA C, HAO X, GAO L, et al. Extracellular Vesicles Released from Macrophages Infected with Mycoplasma pneumoniae Stimulate Proinflammatory Response via the TLR2-NF-κB/JNK Signaling Pathway[J]. Int J Mol Sci, 2023, 24(10): 8588. doi:10.3390/ijms24108588
[21] WANG T, SUN H, LU Z, et al. The CARDS toxin of Mycoplasma pneumoniae induces a positive feedback loop of type 1 immune response[J]. Front Immunol, 2022, 13: 1054788. doi:10.3389/fimmu.2022.1054788
[22] YI X, JIA W, LI W, et al. Diagnostic value of cytokines in severe childhood Mycoplasma pneumoniae pneumonia combined with Adenovirus infection[J]. Ital J Pediatr, 2024, 50(1): 92. doi:10.1186/s13052-024-01661-6
[23] ZHANG M. Improvement of IL-4, IL-6, IL-10, TNF-α and IFN-γ in children with mycoplasma pneumonia through the combination of video scenario-based breathing training and antibiotics[J]. Sleep Breath, 2025, 29(1): 76. doi:10.1007/s11325-025-03244-z
[24] ZHANG Z, DOU H, TU P, et al. Serum cytokine profiling reveals different immune response patterns during general and severe Mycoplasma pneumoniae pneumonia[J]. Front Immunol, 2022, 13: 1088725. doi:10.3389/fimmu.2022.1088725
[25] ISLAM M M, TAKEYAMA N. Role of Neutrophil Extracellular Traps in Health and Disease Pathophysiology: Recent Insights and Advances[J]. Int J Mol Sci, 2023, 24(21): 15805. doi:10.3390/ijms242115805
[26] DEMKOW U. Molecular Mechanisms of Neutrophil Extracellular Trap (NETs) Degradation[J]. Int J Mol Sci, 2023, 24(5): 4896. doi:10.3390/ijms24054896
[27] MA Q, STEIGER S. Neutrophils and extracellular traps in crystal-associated diseases[J]. Trends Mol Med, 2024, 30(9): 809-823. doi:10.1016/j.molmed.2024.05.010
[28] CHOWDHURY C S, KINSELLA R L, MCNEHLAN M E, et al. Type I IFN-mediated NET release promotes Mycobacterium tuberculosis replication and is associated with granuloma caseation[J]. Cell Host Microbe, 2024, 32(12): 2092-2111. doi:10.1016/j.chom.2024.11.008
文章导航

/