Dextramers: new generation of fluorescent MHC class I/peptide multimers for visualization of antigen-specific CD8+ T cells.


Autoria(s): Batard P.; Peterson D.A.; Devêvre E.; Guillaume P.; Cerottini J.C.; Rimoldi D.; Speiser D.E.; Winther L.; Romero P.
Data(s)

2006

Resumo

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.

Identificador

http://serval.unil.ch/?id=serval:BIB_D79B52C290F3

isbn:0022-1759

pmid:16516226

doi:10.1016/j.jim.2006.01.006

isiid:000236494700014

Idioma(s)

en

Fonte

Journal of immunological methods, vol. 310, no. 1-2, pp. 136-148

Palavras-Chave #Antigens, Neoplasm; CD8-Positive T-Lymphocytes/immunology; Dextrans/chemistry; Dextrans/immunology; Epitopes, T-Lymphocyte/immunology; Flow Cytometry; Fluorescent Dyes/chemistry; HLA-A2 Antigen/chemistry; HLA-A2 Antigen/immunology; Humans; Microscopy, Fluorescence; Molecular Weight; Neoplasm Proteins/chemistry; Neoplasm Proteins/immunology; Phosphoproteins/chemistry; Phosphoproteins/immunology; T-Lymphocytes, Cytotoxic/immunology; Trans-Activators/chemistry; Trans-Activators/immunology; Viral Matrix Proteins/chemistry; Viral Matrix Proteins/immunology; Viral Proteins/chemistry; Viral Proteins/immunology
Tipo

info:eu-repo/semantics/article

article