Clinical utility of plasma Epstein-Barr virus DNA monitoring in pediatric Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis: a Chinese retrospective observational study

被引:2
作者
Zhang, Wenzhi [1 ]
Yin, Yuhong [1 ]
Li, Ying [1 ]
Cheng, Li [1 ]
Zhao, Lizhen [1 ]
Peng, Yun [1 ]
Wu, Xiaoyan [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Pediat, Wuhan 430022, Peoples R China
关键词
Epstein-Barr virus DNA; Hemophagocytic lymphohistiocytosis; Prognosis; Pediatric; QUANTITATIVE-ANALYSIS; LOAD;
D O I
10.1186/s13052-024-01689-8
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background Epstein-Barr virus DNA (EBV-DNA) is closely related to the pathogenesis and prognosis of EBV-associated hemophagocytic lymphohistiocytosis (EBV-HLH). The quantitative measurement of blood EBV-DNA is widely used in EBV-HLH, but there remains a lack of evidence to guide clinicians. Methods A retrospective analysis was conducted on clinical manifestations, laboratory tests, 310 blood EBV-DNA loads, and prognosis of 51 pediatric patients diagnosed with EBV-HLH. Receiver operating characteristic (ROC) curves were utilized to determine the optimal cutoff values of EBV-DNA for predicting mortality and evaluating the active status of EBV-HLH. Results EBV-positive- lymphoma-HLH had higher initial plasma EBV-DNA load(1.10 x 10(6)copies/ml) compared to the EBV-HLH group (1.98 x 10(4) copies/ml) (P = 0.006), and experienced recurrently elevated plasma EBV-DNA levels during treatment. The optimal cut-off value of initial plasma EBV-DNA load in predicting mortality was 2.68 x 10(5) copies/ml, with a sensitivity of 88.57% and a specificity of 56.25%. For determining the active status of HLH, the optimal cutoff value of PBMC EBV-DNA load during treatment was 2.95 x 10(5) copies/ml, with a sensitivity of 69.14% and a specificity of 64.71%. The cut-off value of plasma EBV-DNA for determining active status was 1.32 x 10(3) copies/ml, with a sensitivity of 84.34%, and a specificity of 87.67%. Patients with higher PBMC and plasma EBV-DNA at initial and those with repeated elevated plasma EBV-DNA during treatment had worse prognoses (P < 0.05). Conclusion Dynamic monitoring of EBV-DNA is a valuable tool for assessing disease status and predicting the prognosis of EBV-HLH, with plasma EBV-DNA being more effective than PBMC EBV-DNA. Patients with high levels of PBMC and plasma EBV-DNA at initial and those with repeated elevated plasma EBV-DNA during treatment had worse prognoses.
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共 25 条
[11]   EBV Viral Loads in Diagnosis, Monitoring, and Response Assessment [J].
Kimura, Hiroshi ;
Kwong, Yok-Lam .
FRONTIERS IN ONCOLOGY, 2019, 9
[12]  
Liu G-Y, 2021, Am J Cancer Res.
[13]   Viral infections associated with haemophagocytic syndrome [J].
Maakaroun, Nadine Rouphael ;
Moanna, Abeer ;
Jacob, Jesse T. ;
Albrecht, Helmut .
REVIEWS IN MEDICAL VIROLOGY, 2010, 20 (02) :93-105
[14]   Rituximab-containing immuno-chemotherapy regimens are effective for the elimination of EBV for EBV-HLH with only and mainly B lymphocytes of EBV infection [J].
Meng, Guang-Qiang ;
Wang, Jing-Shi ;
Wang, Yi-Ni ;
Wei, Na ;
Wang, Zhao .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2021, 96
[15]   Cell-free EBV DNA as a biomarker during clinical management of nasopharyngeal carcinoma in a nonendemic region [J].
Pramanik, Raja ;
Arora, Shalabh ;
Sharma, Preity ;
Biswas, Ahitagni ;
Nayak, Baibaswata ;
Thakar, Alok ;
Sharma, Atul ;
Ghose, Sampa .
JOURNAL OF MEDICAL VIROLOGY, 2022, 94 (02) :720-728
[16]   A retrospective analysis of EBV-DNA status with the prognosis of lymphoma [J].
Qiu, Lihua ;
Si, Junqi ;
Kang, Junnan ;
Chen, Zehui ;
Nuermaimaiti, Rexidan ;
Qian, Zhengzi ;
Li, Lanfang ;
Zhou, Shiyong ;
You, Mingjian James ;
Zhang, Huilai ;
Tian, Chen .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2022, 26 (20) :5195-5201
[17]  
Ruf S, 2013, EXPERT REV CLIN IMMU, V9, P139, DOI [10.1586/ECI.12.111, 10.1586/eci.12.111]
[18]   T Cell-Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis (HLH) Occurs in Non-Asians and Is Associated with a T Cell Activation State that Is Comparable to Primary HLH [J].
Shamriz, Oded ;
Kumar, Deepak ;
Shim, Jenny ;
Briones, Michael ;
Quarmyne, Maa-Ohui ;
Chonat, Satheesh ;
Lucas, Laura ;
Edington, Holly ;
White, Michael H. ;
Mahajan, Advay ;
Park, Sunita ;
Chandrakasan, Shanmuganathan .
JOURNAL OF CLINICAL IMMUNOLOGY, 2021, 41 (07) :1582-1596
[19]   Characteristics of primary Epstein-Barr virus infection disease spectrum and its reactivation in children, in Suzhou, China [J].
Shi, Ting ;
Huang, Linlin ;
Chen, Zhengrong ;
Tian, Jianmei .
JOURNAL OF MEDICAL VIROLOGY, 2021, 93 (08) :5048-5057
[20]   Quantitative analysis of cell-free Epstein-Barr virus genome copy number in patients with EBV-associated hemophagocytic lymphohistiocytosis [J].
Teramura, T ;
Tabata, Y ;
Yagi, T ;
Morimoto, A ;
Hibi, S ;
Imashuku, S .
LEUKEMIA & LYMPHOMA, 2002, 43 (01) :173-179