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High macrophage activities are associated with advanced periductal fibrosis in chronic Opisthorchis viverrini infection.

Authors :
Salao K
Watakulsin K
Mairiang E
Suttiprapa S
Tangkawattana S
Edwards SW
Sripa B
Source :
Parasite immunology [Parasite Immunol] 2019 Jan; Vol. 41 (1), pp. e12603. Date of Electronic Publication: 2018 Dec 03.
Publication Year :
2019

Abstract

Liver fluke infection caused by Opisthorchis viverrini induces several hepatobiliary conditions including advanced periductal fibrosis (APF) and cholangiocarcinoma (CCA), but >25% of the infected population develops APF and 1% develop CCA. The innate immune response is the first line of defence, and macrophages are critical regulators of fibrosis. We hypothesized that macrophages from infected individuals have different capacities to either promote or suppress periductal fibrosis. We compared phagocytic activities of macrophages of healthy individuals and O viverrini-infected individuals ± APF, and found that macrophages from infected individuals with APF ingested significantly higher numbers of beads compared with healthy controls and O viverrini-infected individuals without APF. To further investigate proteolytic activity, we monitored real-time phagosomal proteolysis of beads conjugated to DQ-BODIPY-BSA using live cell imaging. We show that macrophages from O viverrini-infected individuals with APF also have elevated phagosomal proteolysis activity, which is consistent with their increased phagocytic activity. Additionally, stimulated ROS production by blood monocytes was higher in individuals with APF compared with healthy controls and infected individuals without APF. These results suggest that during O viverrini infection, macrophages with high phagocytic and proteolytic activities together with elevated ROS production are the phenotypes that can promote tissue damage, which results in periductal fibrosis.<br /> (© 2018 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-3024
Volume :
41
Issue :
1
Database :
MEDLINE
Journal :
Parasite immunology
Publication Type :
Academic Journal
Accession number :
30449026
Full Text :
https://doi.org/10.1111/pim.12603