Longitudinal analysis of the impact of rituximab on circulating EBV miRNAs in three paediatric kidney transplant recipients

IF 1.6 Q4 INFECTIOUS DISEASES Journal of clinical virology plus Pub Date : 2023-11-14 DOI:10.1016/j.jcvp.2023.100171
Jaythoon Hassan , Gabriel Gonzalez , Maria Stack , Niamh Dolan , Clodagh Sweeney , Cillian De Gascun , Jeff Connell , Atif Awan , Michael Riordan
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引用次数: 0

Abstract

Background

EBV DNA monitoring is currently the main strategy to identify renal transplant recipients potentially at risk of EBV complications. EBV miRNA expression is markedly altered in different disease presentations associated with EBV. We performed a longitudinal assessment of the impact of rituximab on circulating EBV miRNA in 3 paediatric kidney transplant recipients.

Methods

Forty-two miRNAs encoded within 2 EBV open reading frames (BART and BHRF) were examined over a 28-month period using miRNA qPCR custom panels. EBV DNA was measured using qPCR and lymphocyte subsets were measured by flow cytometry.

Results

Patients were 3 years post kidney transplant and received cycles of rituximab infusions. Treatment with rituximab caused an immediate depletion of the circulating B cells and reduced the expression of the miRNAs and EBV DNA levels. About 4 months post treatment, as the circulating B cells repopulated, EBV miRNAs levels increased. A total of 29 plasma samples were studied and between 4 and 34 EBV miRNAs were detected. A significant correlation was observed between the numbers of EBV miRNAs expressed and the EBV DNA level (r = 0.63, p = 0.001).

Conclusion

We provide an in-depth longitudinal assessment of the impact of rituximab on specific circulating EBV miRNA expression in three paediatric kidney transplant recipients. Rituximab treatment resulted in the reduction of EBV miRNA expression and EBV DNA viral loads. Larger studies are required to determine whether EBV miRNA levels could be useful biomarkers to predict transplant recipients at risk of developing post-transplant lymphoproliferative disease.

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利妥昔单抗对三名儿童肾移植受者循环EBV mirna影响的纵向分析
EBV DNA监测是目前识别有潜在EBV并发症风险的肾移植受者的主要策略。EBV miRNA表达在与EBV相关的不同疾病表现中显着改变。我们对3名儿童肾移植受者的利妥昔单抗对循环EBV miRNA的影响进行了纵向评估。使用miRNA qPCR定制面板对2个EBV开放阅读框(BART和BHRF)内编码的42个miRNA进行了为期28个月的检测。采用qPCR检测EBV DNA,流式细胞术检测淋巴细胞亚群。患者在肾移植后3年接受周期的利妥昔单抗输注。利妥昔单抗治疗引起循环B细胞的立即耗竭,并降低mirna的表达和EBV DNA水平。治疗后约4个月,随着循环B细胞的重新填充,EBV mirna水平升高。共研究了29份血浆样本,检测到4-34种EBV mirna。表达的EBV mirna数量与EBV DNA水平显著相关(r=0.63, p=0.001)。我们提供了一项深入的纵向评估利妥昔单抗对三名儿童肾移植受者特异性循环EBV miRNA表达的影响。利妥昔单抗治疗导致EBV miRNA表达和EBV DNA病毒载量的降低。需要更大规模的研究来确定EBV miRNA水平是否可以作为预测移植受者发生移植后淋巴增殖性疾病风险的有用生物标志物。
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来源期刊
Journal of clinical virology plus
Journal of clinical virology plus Infectious Diseases
CiteScore
2.20
自引率
0.00%
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0
审稿时长
66 days
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