Toll样受体
病毒学
乙型肝炎病毒
寡核苷酸
Toll样受体9
病毒
医学
先天免疫系统
免疫学
生物
免疫系统
基因
基因表达
生物化学
DNA甲基化
作者
Shihyun You,Jared L. Delahaye,Megan E. Ermler,Jennifer S. Singh,William Jordan,Avijit Ray,N. W. Galwey,Daren Austin,Dickens Theodore,Melanie Paff
标识
DOI:10.1016/s0168-8278(22)02041-4
摘要
Conclusion:The concomitant HBsAg declines and ALT elevations indicate that a single, very low dose of IMC-I109V elicited on-target activity consistent with the TCR bispecific (ENVxCD3) mechanism of action, without adverse events.These results are encouraging for the prospect of identifying a tolerable and active treatment regimen with higher and repeat dosing.Enrolment in Part 1 dose escalation continues to evaluate this novel mechanism designed to eliminate HBV-positive hepatocytes.(Eudract no.
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