| Literature DB >> 31363763 |
Mi Sun Moon1, Gabriella Quinn1, Elizabeth C Townsend1, Rabab O Ali1, Grace Y Zhang1, Alyson Bradshaw1, Kareen Hill1, Hannah Guan1, Destanee Hamilton1, David E Kleiner2, Christopher Koh1, Theo Heller1.
Abstract
Hepatitis C virus (HCV) infects 71 million individuals, and barriers to treatment remain. Bacterial translocation is a complication of chronic HCV infection, and this study evaluated circulating microbial components including lipopolysaccharide, peptidoglycan, and β-D-glucan in addition to their pattern recognition receptors and degree of hepatic macrophage uptake. The findings suggest that regulation of serum peptidoglycan and β-D-glucan differs from that of lipopolysaccharide. Additionally, macrophage activation in the liver may be better reflected by the degree of macrophage uptake than by circulating levels of microbial markers. These findings allow for a greater understanding of bacterial translocation and host immune activation during HCV infection. Published by Oxford University Press on behalf of Infectious Diseases Society of America 2019.Entities:
Keywords: bacterial translocation; endotoxin; hepatitis C virus (HCV); macrophage activation
Year: 2019 PMID: 31363763 PMCID: PMC6667717 DOI: 10.1093/ofid/ofz255
Source DB: PubMed Journal: Open Forum Infect Dis ISSN: 2328-8957 Impact factor: 3.835