Ex vivo characterization of allo-MHC-restricted T cells specific for a single MHC-peptide complex.


Autoria(s): Pittet M.J.; Gati A.; Le Gal F.A.; Bioley G.; Guillaume P.; de Smedt M.; Plum J.; Speiser D.E.; Cerottini J.C.; Dietrich P.Y.; Romero P.; Zippelius A.
Data(s)

2006

Resumo

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.

Identificador

http://serval.unil.ch/?id=serval:BIB_9BC901FAC322

isbn:0022-1767

pmid:16455990

isiid:000235180900035

Idioma(s)

en

Fonte

Journal of immunology, vol. 176, no. 4, pp. 2330-2336

Palavras-Chave #Adult; Aged; Aged, 80 and over; Amino Acid Sequence; Child; Child, Preschool; Histocompatibility Antigens/immunology; Humans; Infant; Infant, Newborn; Isoantigens/immunology; Middle Aged; Molecular Sequence Data; Peptides/chemistry; Peptides/immunology; Phenotype; Receptors, Antigen, T-Cell, alpha-beta/chemistry; Receptors, Antigen, T-Cell, alpha-beta/immunology; Substrate Specificity; T-Lymphocytes/immunology; Transplantation, Homologous
Tipo

info:eu-repo/semantics/article

article