THE EXPRESSION OF CARBOHYDRATE ANTIGENS IN ACTIVATED T-CELLS AND IN AUTOIMMUNE-DISEASES

Citation
F. Fortune et al., THE EXPRESSION OF CARBOHYDRATE ANTIGENS IN ACTIVATED T-CELLS AND IN AUTOIMMUNE-DISEASES, Scandinavian journal of immunology, 40(6), 1994, pp. 636-642
Citations number
23
Categorie Soggetti
Immunology
ISSN journal
03009475
Volume
40
Issue
6
Year of publication
1994
Pages
636 - 642
Database
ISI
SICI code
0300-9475(1994)40:6<636:TEOCAI>2.0.ZU;2-C
Abstract
Cell surface carbohydrate antigens have been implicated in cell differ entiation and maturation and may play a role in immunoregulation. The expression of carbohydrates in peripheral blood lymphocytes (PBL) was studied by double immunofluorescence flow cytometry, using MoAbs CT1 a nd CT2 but only a small proportion of cells bound these MoAbs. MoAbs C T1, CT2 and the lectin vicia villosa (VV) which share specificity for Gal NAc were then used to examine lymphocytes from patients with syste mic lupus erythematosus (SLE), rheumatoid arthritis (RA), Behcet's dis ease (BD) and IgA nephropathy. A significant increase in MoAbs CT1 CT2 and VV binding CD4 or CD8 cells was found only with lymphocytes from patients with SLE. However, MoAbs CT or VV binding lymphocytes from he althy subjects were significantly up-regulated by activation with a mi togen (PHA), cross-linked anti-CD3 MoAb or a common antigen (65kDa hea t shock protein), suggesting that an increased proportion of T cells e xpressing these carbohydrates results from any of the three types of l ymphocyte activating agents. Inhibition studies were then carried out to determine the relationship between the MoAbs CT1 and CT2, VV and Ga lNAc. Indeed, VV binding to T cells was significantly inhibited by eit her MoAbs CT1 or CT2, or GalNAc but not GlucNAc, suggesting that VV sh ares a common binding site with MoAb CT and that GalNAc may constitute one of the sugar receptors. Investigations of lymphocytes from adult peripheral blood in health and disease suggest that carbohydrate antig ens may play a role in activation and immunoregulation.