检验医学 ›› 2026, Vol. 41 ›› Issue (6): 554-559.DOI: 10.3969/j.issn.1673-8640.2026.06.006

• 论著 • 上一篇    下一篇

新型鼻咽癌血清标志物P85抗体在低发区EB病毒感染高危人群中的应用价值

葛冬华, 程铖, 沈丽琳, 秦鑫, 高春芳, 高致远(), 徐学文()   

  1. 上海中医药大学附属岳阳中西医结合医院临床检验实验医学中心上海 200437
  • 收稿日期:2026-01-18 修回日期:2026-03-20 出版日期:2026-06-30 发布日期:2026-07-01
  • 通讯作者: 高致远,E-mail:gaozhiyuan20@126.com
    徐学文,E-mail:xuewen-xu@163.com
  • 作者简介:葛冬华,男,1989年生,学士,主管技师,主要从事恶性肿瘤疾病标志物研究。
  • 基金资助:
    国家自然科学基金项目(82372321);上海市卫生健康委协同创新集群项目(2019CXJQ03);北京热景科技项目(KY111.40.214)

Application value of a novel serum biomarker P85 antibody for nasopharyngeal carcinoma in high-risk populations of Epstein-Barr virus infection in low-incidence areas

GE Donghua, CHENG Cheng, SHEN Lilin, QIN Xin, GAO Chunfang, GAO Zhiyuan(), XU Xuewen()   

  1. Clinical Laboratory Medicine CenterYueyang Hospital of Integrated Traditional Chinese and Western Medicine,Shanghai University of Traditional Chinese MedicineShanghai 200437, China
  • Received:2026-01-18 Revised:2026-03-20 Online:2026-06-30 Published:2026-07-01

摘要:

目的 探讨新型鼻咽癌(NPC)标志物P85抗体在NPC低发地区高危人群筛查中的价值及其对NPC的诊断效能。方法 选取2024年1月—2025年12月上海中医药大学附属岳阳中西医结合医院156例高危患者(其中非NPC140例、NPC16例),高危人群定义:血浆EB病毒(EBV)DNA阳性(≥400 拷贝·mL-1),且血清EBV衣壳抗原(VCA)IgA抗体和/或核抗原1(NA1)IgA抗体阳性。收集所有研究对象的临床资料和EBV感染相关指标(血浆EBV DNA载量和血清EBV相关抗体)检测结果,并检测P85抗体水平。采用受试者工作特征(ROC)曲线评价各项指标诊断NPC的效能。为避免小样本过拟合,采用5种交叉验证方法(K折法、留一法、留组法、自举法、分层K折法)对诊断效能进行内部验证,计算校正后的曲线下面积(AUC)和95%可信区间(CI)。结果 NPC组血清P85抗体水平显著高于对照组(P<0.001),2个组之间血浆EBV DNA载量、NA1 IgA抗体和VCA IgA抗体水平差异均无统计学意义(P>0.05)。 EBV DNA、NA1 IgA抗体、VCA IgA抗体、P85抗体诊断NPC的AUC分别为0.514、0.587、0.633、0.916。经5种交叉验证方法(K折法、留一法、留组法、自举法、分层K折法)验证后,P85抗体的校正AUC分别为0.879、0.874、0.919、0.910、0.898,不同方法之间的AUC波动较小;而EBV DNA、NA1 IgA抗体、VCA IgA抗体的AUC分别为0.543~0.770、0.542~0.860、0.482~0.654,不同方法之间AUC波动较大。结论 P85抗体在NPC低发地区高危人群中具有较高的特异性,可作为低发地区NPC新型的诊断标志物。

关键词: P85抗体, Epstein-Barr病毒, 鼻咽癌, 高危人群, 交叉验证

Abstract:

Objective To investigate the value of the novel nasopharyngeal carcinoma(NPC) biomarker P85 antibody in screening high-risk individuals in low-incidence areas and its diagnostic efficacy for NPC. Methods A total of 156 high-risk patients(140 non-NPC and 16 NPC cases) were enrolled from Yueyang Hospital of Integrated Traditional Chinese and Western Medicine of Shanghai University of Traditional Chinese Medicine from January 2024 to December 2025. High-risk individuals were defined as those with positive plasma Epstein-Barr virus(EBV) DNA(≥400 copies·mL-1) and positive serum EBV viral capsid antigen(VCA) IgA antibody and/or nuclear antigen 1(NA1) IgA antibody. The clinical data and EBV infection-related indicators(plasma EBV DNA load and serum EBV-related antibodies) were collected,and P85 antibody levels were determined. The diagnostic efficacy of each indicator for NPC was evaluated using receiver operating characteristic(ROC) curve. To avoid overfitting in small samples,5 cross-validation methods(K-fold,leave-one-out,leave-group-out,bootstrap and stratified K-fold) were used to internally validate the diagnostic efficacy,and the corrected area under curve(AUC) and 95% confidence interval(CI) were calculated. Results The serum P85 antibody level in NPC group was higher than that in control group(P<0.001),while there was no statistical significance in plasma EBV DNA load,NA1 IgA antibody and VCA IgA antibody levels between the 2 groups(P>0.05). The AUC for diagnosing NPC by EBV DNA,NA1 IgA antibody,VCA IgA antibody and P85 antibody were 0.514,0.587,0.633 and 0.916,respectively. After validation by 5 cross-validation methods(K-fold,leave-one-out,leave-group-out,bootstrap and stratified K-fold),the corrected AUC of P85 antibody were 0.879,0.874,0.919,0.910 and 0.898,respectively,with small fluctuations among different methods. The AUC of EBV DNA,NA1 IgA antibody and VCA IgA antibody ranged from 0.543 to 0.770,0.542 to 0.860 and 0.482 to 0.654,respectively,with large fluctuations among different methods. Conclusions P85 antibody has high specificity in high-risk individuals in low-incidence areas of NPC and can be used as a novel diagnostic marker for NPC in such areas.

Key words: P85 antibody, Epstein-Barr virus, Nasopharyngeal carcinoma, High-risk population, Cross-validation

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