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Ex Vivo Characterization of Allo-MHC-Restricted T Cells Specific for a Single MHC-Peptide Complex
Author(s) -
Mikaël J. Pittet,
Asma Gati,
Frederic-Anne Le Gal,
Gilles Bioley,
Philippe Guillaume,
Magda De Smedt,
Jean Plum,
Daniel E. Speiser,
JeanCharles Cerottini,
PierreYves Dietrich,
Pedro Romero,
Alfred Zippelius
Publication year - 2006
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.176.4.2330
Subject(s) - ex vivo , streptamer , cd8 , biology , cytotoxic t cell , major histocompatibility complex , mhc class i , microbiology and biotechnology , flow cytometry , avidity , t cell , immunology , antigen presenting cell , immune system , interleukin 21 , in vivo , antigen , in vitro , genetics
Alloreactive T cells are thought to be a potentially rich source of high-avidity T cells with therapeutic potential since tolerance to self-Ags is restricted to self-MHC recognition. Given the particularly high frequency of alloreactive T cells in the peripheral immune system, we used numerous MHC class I multimers to directly visualize and isolate viral and tumor Ag-specific alloreactive CD8 T cells. In fact, all but one specificities screened were undetectable in ex vivo labeling. In this study, we report the occurrence of CD8 T cells specifically labeled with allo-HLA-A*0201/Melan-A/MART-1(26-35) multimers at frequencies that are in the range of 10(-4) CD8 T cells and are thus detectable ex vivo by flow cytometry. We report the thymic generation and shaping of tumor Ag-specific, alloreactive T cells as well as their fate once seeded in the periphery. We show that these cells resemble their counterparts in HLA-A*0201-positive individuals, based on their structural and functional attributes.

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