Reversible HLA multimers ( Streptamers) for the isolation of human cytotoxic T lymphocytes functionally active against tumor- and virus-derived antigens

The development of MHC/peptide multimers has facilitated the visualization and purification of antigen-specific T cells. However, the persistence of multimers leads to prolonged T cell receptor signaling and subsequently to altered T-cell function. We have recently developed a new type of MHC/peptid...

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Veröffentlicht in:Journal of immunological methods 2007-03, Vol.320 (1), p.119-131
Hauptverfasser: Neudorfer, Julia, Schmidt, Burkhard, Huster, Katharina M., Anderl, Florian, Schiemann, Matthias, Holzapfel, Gerd, Schmidt, Thomas, Germeroth, Lothar, Wagner, Hermann, Peschel, Christian, Busch, Dirk H., Bernhard, Helga
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Sprache:eng
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Zusammenfassung:The development of MHC/peptide multimers has facilitated the visualization and purification of antigen-specific T cells. However, the persistence of multimers leads to prolonged T cell receptor signaling and subsequently to altered T-cell function. We have recently developed a new type of MHC/peptide multimers, which can be dissociated from the T cell. Herein, we have generated and tested for the first time reversible HLA/peptide multimers, termed Streptamers, for the isolation of human T cells. The Streptamer technique demonstrates the specificity and sensitivity of conventional HLA/peptide tetramers with regards to the sorting of human T lymphocytes. This is shown for T cells directed against immunogenic peptides derived from viral and tumor-associated antigens. We show that antigen-specific cytotoxic T cells remain functionally active following Streptamer dissociation, whereas lytic function and proliferation of the T cells is impaired in the presence of conventional tetramers. These novel HLA/peptide Streptamer reagents allow the isolation of antigen-specific T cells with preserved function and, therefore, facilitate the development of adoptive T cell transfer regimens for the treatment of patients with cancer or infectious diseases.
ISSN:0022-1759
1872-7905
DOI:10.1016/j.jim.2007.01.001