| Literature DB >> 16516226 |
Pascal Batard1, Daniel A Peterson, Estelle Devêvre, Philippe Guillaume, Jean-Charles Cerottini, Donata Rimoldi, Daniel E Speiser, Lars Winther, Pedro Romero.
Abstract
Direct identification as well as isolation of antigen-specific T cells became possible since the development of "tetramers" based on avidin-fluorochrome conjugates associated with mono-biotinylated class I MHC-peptide monomeric complexes. In principle, a series of distinct class I MHC-peptide tetramers, each labelled with a different fluorochrome, would allow to simultaneously enumerate as many unique antigen-specific CD8(+) T cells. Practically, however, only phycoerythrin and allophycocyanin conjugated tetramers have been generally available, imposing serious constraints for multiple labeling. To overcome this limitation, we have developed dextramers which are multimers based on a dextran backbone bearing multiple fluorescein and streptavidin moieties. Here we demonstrate the functionality and optimization of these new probes on human CD8(+) T cell clones with four independent antigen specificities. Their applications to the analysis of relatively low frequency antigen-specific T cells in peripheral blood, as well as their use in fluorescence microscopy, are demonstrated. The data show that dextramers produce a stronger signal than their fluoresceinated tetramer counterparts. Thus, these could become the reagents of choice as the antigen-specific T cell labeling transitions from basic research to clinical application.Entities:
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Year: 2006 PMID: 16516226 DOI: 10.1016/j.jim.2006.01.006
Source DB: PubMed Journal: J Immunol Methods ISSN: 0022-1759 Impact factor: 2.303