Publication | Open Access
Cutting Edge: CD1a Tetramers and Dextramers Identify Human Lipopeptide–Specific T Cells Ex Vivo
68
Citations
23
References
2013
Year
Microbial PathogensAdaptive Immune SystemImmunologyImmune RegulationImmunodominanceImmunologic MechanismAntigen ProcessingCd4 T Cell ResponsesImmunotherapeuticsInnate ImmunitySoluble TcrImmune SystemForeign Ag RecognitionCd1a TetramersHuman Cd1aCell SignalingRegulatory T Cell BiologyImmune SurveillanceT Cell ImmunityCell BiologyLipopeptidesCellular Immune ResponseMedicine
Human CD1a mediates foreign Ag recognition by a T cell clone, but the nature of possible TCR interactions with CD1a/lipid are unknown. After incubating CD1a with a mycobacterial lipopeptide Ag, dideoxymycobactin (DDM), we identified and measured binding to a recombinant TCR (TRAV3/ TRBV3-1, KD of ≈100 μM). Detection of ternary CD1a/lipid/TCR interactions enabled development of CD1a tetramers and CD1a multimers with carbohydrate backbones (dextramers), which specifically stained T cells using a mechanism that was dependent on the precise stereochemistry of the peptide backbone and was blocked with a soluble TCR. Furthermore, sorting of human T cells from unrelated tuberculosis patients for bright DDM-dextramer staining allowed recovery of T cells that were activated by CD1a and DDM. These studies demonstrate that the mechanism of T cell activation by lipopeptides occurs via ternary interactions of CD1a/Ag/TCR. Furthermore, these studies demonstrate the existence of lipopeptide-specific T cells in humans ex vivo.
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