Murdoch University Research Repository

Welcome to the Murdoch University Research Repository

The Murdoch University Research Repository is an open access digital collection of research
created by Murdoch University staff, researchers and postgraduate students.

Learn more

Ultra-sensitive class I tetramer analysis reveals previously undetectable populations of antiviral CD8+ T cells

Barnes, E., Ward, S.M., Kasprowicz, V.O., Dusheiko, G., Klenerman, P. and Lucas, M. (2004) Ultra-sensitive class I tetramer analysis reveals previously undetectable populations of antiviral CD8+ T cells. European Journal of Immunology, 34 (6). pp. 1570-1577.

Free to read: https://doi.org/10.1002/eji.200424898
*No subscription required

Abstract

A major breakthrough in cellular immunology has been the development of HLA class I tetramers to analyze CD8+ T cell responses. However, in many situations, including persistent virusinfection, specific T cell responses are rarely detected using this technology. This raises the question of whether such responses are ‘deleted’ (or ‘exhausted’) or present below the conventional detection limit for class I tetramer staining. In particular, persistent hepatitis C virus (HCV) infection is characterized by very weak or apparently absent specific CD8+ T cell responses, even though they are readily detectable in acute disease. Therefore, we assessed the use of anti-PE-labeled magnetic beads to enrich tetramer-positive HCV-specific T cells and identify previously undetectable populations. Using the enrichment technique, HCV-specific T cells could be detected in the majority of infected individuals, whereas these responses were not detected using conventional tetramer staining (8/15 vs. 1/15; p=0.01). Magnetic enrichment could reliably detect very rare HCV-specific responses at frequencies of >0.0011% of CD8+ T cells (∼1/million PBMC), and phenotypic analysis of these rare populations was possible. Therefore, this direct ex vivo technique revealed the persistence of very low frequencies of virus-specific CD8+ T cells during chronic virus infection and is readily transferable to the study of other viral, self- or tumor-specific T cells.

Item Type: Journal Article
Murdoch Affiliation(s): Institute for Immunology and Infectious Diseases
Publisher: John Wiley & Sons Ltd.
Copyright: © John Wiley & Sons, Inc.
URI: http://researchrepository.murdoch.edu.au/id/eprint/37290
Item Control Page Item Control Page