转录组
干扰素
慢性肝炎
免疫学
聚乙二醇干扰素
病毒学
人口
α-干扰素
医学
发病机制
生物
免疫系统
基因
病毒
利巴韦林
基因表达
遗传学
环境卫生
作者
Upkar S. Gill,Dimitra Peppa
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2023-09-01
卷期号:79 (1): 18-20
标识
DOI:10.1097/hep.0000000000000560
摘要
Pegylated-Interferon alpha (PegIFN-α) is a treatment option for chronic hepatitis B (CHB) but has limited efficacy. It has both immune modulatory and antiviral capacity, however the mechanisms of PegIFN-α in relation to CHB pathogenesis remain understudied. The current editorial reviews a recent study related to the in-vivo use of PegIFN-α using single-cell RNA sequencing (scRNA-seq) technology. PegIFN-α reverts the transcriptome profile of treated samples close to that of the healthy population, diminishing the pro-inflammatory genes and ‘inflammatory scores’ which will be important for the HBV-cure program.
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