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Interferon alpha induces a stronger antiviral effect than interferon lambda in HBV/HDV infected humanized mice.
- Source :
-
Virus research [Virus Res] 2024 Nov; Vol. 349, pp. 199451. Date of Electronic Publication: 2024 Aug 26. - Publication Year :
- 2024
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Abstract
- Recent studies indicate that treatment of chronic hepatitis D virus (HDV) with either pegylated interferon (IFN)λ or pegylated IFNα monotherapy leads to a dramatic decline in HDV RNA. Herein, we investigated the innate antiviral efficacy of IFNλ and IFNα in humanized mice that lack an adaptive immune response. Humanized mice were either co-infected with hepatitis B virus (HBV) and HDV simultaneously, or HDV infection was performed subsequent to HBV infection (i.e., superinfected). After steady viral replication was achieved, mice received either IFNλ (n = 6) or IFNα (n = 7) for 12 (or 13) weeks. Pretreatment median levels of serum HBV DNA (8.8 [IQR:0.2] log IU/ml), HDV RNA (9.8 [0.5] log IU/ml), HBsAg (4.0 [0.4] log IU/ml) and human albumin, hAlb (6.9 [0.1] log ng/mL) were similar between mice treated with IFNα or IFNλ and between those coinfected versus superinfected. Compared to mice treated with IFNλ, mice treated with IFNα had a significantly greater decline in HBV, HDV, and HBsAg levels. In conclusion, IFNα induces stronger inhibition of HBV and HDV than IFNλ in humanized mice that lack an adaptive immune response. Further studies are needed to assess the respective role of the combined innate-and adaptive-immune systems in the treatment of HBV and HDV with IFNα and IFNλ.<br />Competing Interests: Declaration of competing interest Kazuaki Chayama has received honoraria from Bristol-Myers Squibb and MSD K.K., AbbVie, Gilead Science, Dainippon Sumitomo Pharma and Mitsubishi Tanabe Pharma and research funding from Gilead Science, Dainippon Sumitomo Pharma, MSD K.K., AbbVie, Eisai, TORAY, Otsuka Pharma, Chugai Pharma, Takeda Pharma and Roche. Jeffrey Glenn, director, and equity holder of Eiger Biopharmaceuticals. Ohad Etzion has received consulting fees from Eiger Biopharmaceuticals. The other authors declare no conflicts of interest that pertain to this work.<br /> (Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Mice
Humans
Virus Replication drug effects
Hepatitis D, Chronic drug therapy
Hepatitis D, Chronic virology
Coinfection drug therapy
Coinfection virology
Interferons
Hepatitis B drug therapy
Hepatitis B virology
Hepatitis B immunology
Hepatitis D drug therapy
Hepatitis D virology
Hepatitis D immunology
RNA, Viral blood
DNA, Viral blood
Hepatitis B, Chronic drug therapy
Hepatitis B, Chronic immunology
Hepatitis B, Chronic virology
Viral Load drug effects
Interferon-alpha therapeutic use
Interferon-alpha pharmacology
Antiviral Agents therapeutic use
Antiviral Agents pharmacology
Hepatitis Delta Virus drug effects
Hepatitis B virus drug effects
Hepatitis B virus immunology
Disease Models, Animal
Subjects
Details
- Language :
- English
- ISSN :
- 1872-7492
- Volume :
- 349
- Database :
- MEDLINE
- Journal :
- Virus research
- Publication Type :
- Academic Journal
- Accession number :
- 39168375
- Full Text :
- https://doi.org/10.1016/j.virusres.2024.199451