Chemokine-Regulated Recruitment of Antigen-Specific T-Cell Subpopulations to the Liver in Acute and Chronic Hepatitis C Infection

Chemokine-Regulated Recruitment of Antigen-Specific T-Cell Subpopulations to the Liver in Acute and Chronic Hepatitis C Infection.

Full text not available from this repository.
Item Type: Article
Status: Published
Official URL: https://doi.org/10.1093/infdis%2Fjiy679
Journal or Publication Title: The Journal of Infectious Diseases
Volume: 219
Number: 9
Page Range: pp. 1430-1438
Date: 2018
Divisions: Melanoma Oncology and Immunology
Depositing User: General Admin
Identification Number: 10.1093/infdis/jiy679
ISSN: 0022-1899
Date Deposited: 21 Dec 2020 22:48
Abstract:

Background: In hepatitis C virus (HCV) infection, virus-specific CD8+ T cells are recruited to the liver for antiviral activity. Multiple chemokine ligands are induced by the infection, notably interferon-inducible chemokine, CXCL10. In HCV, intrahepatic T cells express chemokine receptors (CCRs), including CXCR3, CXCR6, CCR1, and CCR5, but CCR expression on antigen-specific effector and memory T cells has not been investigated.

Methods: Paired blood and liver samples were collected from subjects with chronic HCV for flow cytometric analysis of CCR expression on CD8+ T cells. Expression of these CCRs was then examined on HCV-specific CD8+ T-cell subpopulations in the blood from subjects with acute or chronic HCV.

Results: Relative to peripheral blood, the liver was enriched with CD8+ T cells expressing CCR2, CCR5, CXCR3, and CXCR6 either singly or in combinations. CXCR3 was preferentially expressed on HCV-specific CD8+ T cells in both acute and chronic phases of infection in blood. Both CXCR3 and CCR2 were overexpressed on HCV-specific CD8+CCR7+CD45RO+ (central memory) cells, whereas effector memory (CD8+CCR7-CD45RO+) cells expressed more CXCR6.

Conclusions: CXCR3-mediated signals support the accumulation of HCV-specific CD8+ memory T cells in the infected liver, and emphasize the importance of the CXCL10/CXCR3 trafficking pathway during acute and chronic HCV infection.

Keywords: CD8+ T cells; CXCR3; chemokine receptor; hepatitis C; liver.

© The Author(s) 2018. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Creators:
Creators
Email
Pirozyan, Mehdi R
UNSPECIFIED
Nguyen, Nam
UNSPECIFIED
Cameron, Barbara
UNSPECIFIED
Luciani, Fabio
UNSPECIFIED
Bull, Rowena A
UNSPECIFIED
Zekry, Amany
UNSPECIFIED
Lloyd, Andrew R
UNSPECIFIED
Last Modified: 21 Dec 2020 22:48
URI: https://eprints.centenary.org.au/id/eprint/224

Actions (login required)

View Item View Item