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A Transgenic Mouse Model Genetically Tags All Activated CD8 T Cells
Author(s) -
Charles H. Maris,
Joseph D. Miller,
John D. Altman,
Joshy Jacob
Publication year - 2003
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.171.5.2393
Subject(s) - lymphocytic choriomeningitis , biology , cytotoxic t cell , cd8 , epitope , transgene , effector , genetically modified mouse , major histocompatibility complex , t cell , population , virology , microbiology and biotechnology , antigen , immunology , genetics , immune system , gene , in vitro , demography , sociology
Identifying and characterizing Ag-specific CD8+ T cells are central to the study of immunological memory. Although powerful strategies such as MHC tetramers and peptide-induced cytokine production assays exist for identifying Ag-specific CD8+ T cells, alternate strategies that are not dependent upon a priori knowledge of the immunodominant and subdominant antigenic epitopes, as well as the MHC background of the animal are of obvious utility. In this study, we present a transgenic mouse model that uses Cre-loxP recombination to permanently mark all activated CD8+ T cells with beta-galactosidase. We used the lymphocytic choriomeningitis virus infection model to track the dynamics of the antiviral CD8+ T cell responses. We show that in this transgenic mouse model system, all of the antiviral effector and memory CD8+ T cells are contained within the beta-gal-marked CD8+ T cell population.

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