CD11b expression as a marker to distinguish between recently activated effector CD8+ T cells and memory cells
Author(s) -
Jeanette Erbo Christensen,
Susanne Ørding Andreasen,
Jan Pravsgaard Christensen,
Allan Randrup Thomsen
Publication year - 2001
Publication title -
international immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.86
H-Index - 134
eISSN - 1460-2377
pISSN - 0953-8178
DOI - 10.1093/intimm/13.4.593
Subject(s) - lymphocytic choriomeningitis , biology , effector , cytotoxic t cell , cd8 , interleukin 21 , microbiology and biotechnology , zap70 , il 2 receptor , streptamer , antigen , t cell , immunology , immune system , in vitro , biochemistry
CD8(+) T cells in different activation states have been difficult to identify phenotypically. In this study we have investigated whether Mac-1 (CD11b) expression can be used as a criterion to distinguish between recently activated effector cells and memory cells belonging to the CD8(+) T cell subset. Polyclonal virus-specific effector and memory CD8(+) T cells from lymphocytic choriomeningitis- and vesicular stomatitis virus-infected mice were visualized through staining for intracellular IFN-gamma or binding of MHC-peptide tetramers, and Mac-1 expression was evaluated. Naive T cells and most virus-specific memory CD8(+) T cells express little or no Mac-1 independent of the virus model employed. In contrast, the majority of CD8(+) T cells present during acute infection express a significant level of Mac-1 and, similarly, Mac-1 expression is found on secondary effectors generated in response to viral re-exposure. We therefore suggest that high Mac-1 expression defines a subset of circulating effector cells and that the presence of this marker on antigen-specific CD8(+) T cells signifies recent activation.
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