Association of Mutations in Toll-like Receptor 2 Signaling Genes With Fulminant Form of Hepatitis B–Related Acute Liver Failure

• Published in: The Journal of infectious diseases Vol. 215; no. 8; pp. 1221 - 1230
• Main Authors: Han, Yue, Gu, Leilei, Liu, Jing, Li, Xinhua, Wang, Mingjie, Gong, Qiming, Yu, Demin, Yang, Zhitao, Zhang, Donghua, Yang, Huijuan, Shen, Zhongliang, Zhu, Hongguang, Xie, Youhua, Zhang, Xinxin
• Format: Journal Article
• Language: English
• Published: US Oxford University Press 15.04.2017
• Subjects: Adult; Alanine Transaminase - metabolism; Animals; DNA, Viral - genetics; Female; Hepatitis B - complications; Hepatitis B Core Antigens - blood; Hepatitis B virus; Humans; Liver - virology; Liver Failure, Acute - genetics; Liver Failure, Acute - virology; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Middle Aged; Mutation; PATHOGENESIS AND HOST RESPONSE; Signal Transduction; T-Lymphocytes, Regulatory - metabolism; Toll-Like Receptor 2 - genetics; Young Adult; pathway enrichment; hepatitis B; FHB-ALF; TLR2
• ISSN: 0022-1899; 1537-6613
• DOI: 10.1093/infdis/jix097

Background. The fulminant form of hepatitis B–related acute liver failure (FHB-ALF) is a rare but highly fatal outcome of acute hepatitis B virus (HBV) infection. Its related host factors have not been studied to our knowledge. Methods. To identify functionally relevant biological pathway(s) in FHB-ALF pathogenesis, pathway enrichment analysis was conducted on a data set of rare case-specific variants derived from exomic sequencing of 10 unrelated cases. Key variants in identified pathways were validated using 312 controls with HBV disease. Mechanistic studies of a recurrent Toll-like receptor (TLR) 2 gene (TLR2) variant were performed in vitro and in vivo. Results. The TLR signaling pathway was highly enriched, with associated variants found in 9 of the 10 cases. Notably, a rare heterozygous single-nucleotide variation causing F679I on in TLR2 F679I was identified in 2 unrelated cases. In vitro analysis demonstrated F679I to cause loss of function. In both heterozygous and homozygous TLR2 knockout mice, injection of HBV replicon plasmid resulted in more prominent alanine aminotransferase elevations and hepatic necroinflammation than in wild-type mice. Mechanistic analyses demonstrated reduced regulatory T-cell percentages in postexposure TLR2 knockout mice. Conclusions. TLR2 signaling is very likely impaired in patients with FHB-ALF. The recurrence of rare case-specific TLR2 variant strongly suggests mechanistic contribution to fulminancy in HBV infection.