Variable Patterns of Programmed Death-1 Expression on Fully Functional Memory T Cells after Spontaneous Resolution of Hepatitis C Virus Infection

Author:

Bowen David G.1,Shoukry Naglaa H.2,Grakoui Arash3,Fuller Michael J.1,Cawthon Andrew G.1,Dong Christine4,Hasselschwert Dana L.5,Brasky Kathleen M.6,Freeman Gordon J.7,Seth Nilufer P.8,Wucherpfennig Kai W.8,Houghton Michael4,Walker Christopher M.19

Affiliation:

1. Center for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio

2. University of Montreal Hospital Centre (CHUM) and Department of Medicine, University of Montreal, Montreal, Quebec, Canada

3. Emory University, Atlanta, Georgia

4. Novartis Corporation, Emeryville, California

5. New Iberia Research Center, New Iberia, Louisiana

6. Southwest Foundation for Biomedical Research, San Antonio, Texas

7. Department of Medical Oncology

8. Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts

9. College of Medicine and Public Health, Ohio State University, Columbus, Ohio

Abstract

ABSTRACT The inhibitory receptor programmed death-1 (PD-1) is present on CD8 + T cells in chronic hepatitis C virus (HCV), but expression patterns in spontaneously resolving infections are incompletely characterized. Here we report that PD-1 was usually absent on memory CD8 + T cells from chimpanzees with resolved infections, but sustained low-level expression was sometimes observed in the absence of apparent virus replication. PD-1-positive memory T cells expanded and displayed antiviral activity upon reinfection with HCV, indicating conserved function. This animal model should facilitate studies of whether PD-1 differentially influences effector and memory T-cell function in resolved versus persistent human infections.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference22 articles.

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