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Ledipasvir/sofosbuvir and ribavirin for the treatment of ribavirin-refractory persistent hepatitis E virus infection
被引:2
|作者:
Gallacher, Jennifer
[1
,2
]
Taha, Yusri
[1
]
Filipe, Ana da Silva
[3
]
Ijaz, Samreen
[4
]
McPherson, Stuart
[1
,2
,5
]
机构:
[1] Newcastle Upon Tyne Hosp NHS Fdn Trust, Viral Hepatitis Serv, Newcastle Upon Tyne, England
[2] Newcastle Univ, Translat & Clin Res Inst, Newcastle Upon Tyne, England
[3] Univ Glasgow, MRC, Ctr Virus Res, Glasgow, Scotland
[4] UK Hlth Secur Agcy, Blood Borne Virus Unit, London, England
[5] Newcastle Upon Tyne Hosp NHS Fdn Trust, Freeman Hosp, Liver Unit, Newcastle Upon Tyne NE7 7DN, England
来源:
基金:
英国医学研究理事会;
关键词:
Hepatitis E virus;
Treatment;
Antiviral resistance;
Chronic infection;
Immunosuppressed;
REPLICATION;
D O I:
10.1016/j.idcr.2023.e01741
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Persistent Hepatitis E Virus infection (HEV) is a rare but increasingly recognised condition in immunocompro-mised individuals. Untreated, this infection can rapidly progress to cirrhosis. Ribavirin is recommended as the first line treatment and the majority achieve sustained viral clearance. However, treatment options are limited for those who fail ribavirin. We report a case of a patients with ribavirin-refractory persistent HEV who responded to ledipasvir/sofosbuvir and ribavirin treatment. This patients had failed 2 course of ribavirin and 1 course of PEG-Interferon and ribavirin and he was known to harbour ribavirin-associated mutations (G1634R, D1384G and K1383N) in the RNA dependent RNA polymerase. He was treated with ledipasvir/sofosbuvir (LDV/ SOF; Harvoni 90/400 mg) and ribavirin (R) 400 mg twice daily for 32 weeks. At treatment initiation his HEV RNA was 1.1 x 106 IU/ML and reduced to 1.8 x 104 IU/ML and 43 IU/ML at one and four weeks of treatment, respectively, becoming not detected in blood and stool by week eight. His blood HEV RNA remained unde-tectable for seven months after treatment completion. Unfortunately, at eight months post-treatment, his blood HEV RNA became detectable at a low level (35 IU/ML). His stool HEV RNA was also detectable at 620 IU/ML consistent with a late relapse. He restarted LDV/SOF+R and by week four of treatment HEV RNA was not detected in blood and stool. He remains on treatment. In conclusion, this is the first report demonstrating the antiviral activity of LDV/SOF+R in the treatment of persistent HEV infection.
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