Suppr超能文献

肝移植患者接受利巴韦林治疗后的血浆戊型肝炎病毒动力学。

Plasma Hepatitis E Virus Kinetics in Solid Organ Transplant Patients Receiving Ribavirin.

机构信息

National Reference Center for Hepatitis E, Department of Virology, Federative Institute of Biology, CHU Purpan, INSERM U1043, University Toulouse III-Paul Sabatier, 31300 Toulouse, France.

The Program for Experimental & Theoretical Modeling, Division of Hepatology, Loyola University Medical Center, Maywood, IL 60153, USA.

出版信息

Viruses. 2019 Jul 9;11(7):630. doi: 10.3390/v11070630.

Abstract

Hepatitis E virus (HEV) infection causes chronic hepatitis in solid organ transplant (SOT) recipients. Antiviral therapy consists of three months of ribavirin, although response rates are not optimal. We characterized plasma HEV kinetic patterns in 41 SOT patients during ribavirin therapy. After a median pharmacological delay of three (range: 0-21) days, plasma HEV declined from a median baseline level of 6.12 (3.53-7.45) log copies/mL in four viral kinetic patterns: (i) monophasic ( = 18), (ii) biphasic ( = 13), (iii) triphasic ( = 8), and (iv) flat-partial response ( = 2). The mean plasma HEV half-life was estimated to be 2.0 ± 0.96 days. Twenty-five patients (61%) had a sustained virological response (SVR) 24 weeks after completion of therapy. Viral kinetic patterns (i)-(iii) were not associated with baseline characteristics or outcome of therapy. A flat-partial response was associated with treatment failure. All patients with a log concentration decrease of plasma HEV at day seven of >15% from baseline achieved SVR. In conclusion, viral kinetic modeling of plasma HEV under ribavirin therapy showed, for the first time, four distinct kinetic profiles, a median pharmacologic delay of three days, and an estimated HEV half-life of two days. Viral kinetic patterns were not associated with response to therapy, with the exception of a flat-partial response.

摘要

戊型肝炎病毒(HEV)感染可导致实体器官移植(SOT)受者发生慢性肝炎。抗病毒治疗包括三个月的利巴韦林,但应答率并不理想。我们在 41 名 SOT 患者接受利巴韦林治疗期间对其血浆 HEV 动力学模式进行了特征描述。在中位药理学延迟 3 天(范围:0-21 天)后,血浆 HEV 从基线水平中位数 6.12(3.53-7.45)log 拷贝/ml 下降,有四种病毒动力学模式:(i)单相(=18),(ii)双相(=13),(iii)三相(=8)和(iv)平坦-部分应答(=2)。平均血浆 HEV 半衰期估计为 2.0±0.96 天。25 名患者(61%)在治疗结束后 24 周时获得持续病毒学应答(SVR)。动力学模式(i)-(iii)与基线特征或治疗结果无关。平坦-部分应答与治疗失败相关。所有在第 7 天血浆 HEV 对数浓度下降基线值的>15%的患者均获得 SVR。总之,首次在接受利巴韦林治疗的血浆 HEV 病毒动力学模型中显示了四种不同的动力学特征、中位药理学延迟 3 天以及估计的 HEV 半衰期为 2 天。除了平坦-部分应答外,病毒动力学模式与治疗应答无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c74d/6669701/1014a4a0377c/viruses-11-00630-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验