Ultra-sensitive class I tetramer analysis reveals previously undetectable populations of antiviral CD8 super(+) T cells
A major breakthrough in cellular immunology has been the development of HLA class I tetramers to analyze CD8 super(+) 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 w...
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Published in | European journal of immunology Vol. 34; no. 6; pp. 1570 - 1577 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
01.01.2004
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Subjects | |
Online Access | Get full text |
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Summary: | A major breakthrough in cellular immunology has been the development of HLA class I tetramers to analyze CD8 super(+) 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 super(+) 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 super(+) 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 super(+) T cells during chronic virus infection and is readily transferable to the study of other viral, self- or tumor-specific T cells. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-2 |
ISSN: | 0014-2980 |
DOI: | 10.1002/eji.200424898 |