Cutting edge: monovalency of CD28 maintains the antigen dependence of T cell costimulatory responses. - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Journal of Immunology Année : 2006

Cutting edge: monovalency of CD28 maintains the antigen dependence of T cell costimulatory responses.

Résumé

CD28 and CTLA-4 are the major costimulatory receptors on naive T cells. But it is not clear why CD28 is monovalent whereas CTLA-4 is bivalent for their shared ligands CD80/86. We generated bivalent CD28 constructs by fusing the extracellular domains of CTLA-4 or CD80 with the intracellular domains of CD28. Bivalent or monovalent CD28 constructs were ligated with recombinant ligands with or without TCR coligation. Monovalent CD28 ligation did not induce responses unless the TCR was coligated. By contrast, bivalent CD28 ligation induced responses in the absence of TCR engagement. To extend these findings to primary cells, we used novel superagonistic and conventional CD28 Abs. Superagonistic Ab D665, but not conventional Ab E18, predominantly ligates CD28 bivalently at low CD28/Ab ratios and induces Ag-independent T cell proliferation. Monovalency of CD28 for its natural ligands is thus essential to provide costimulation without inducing responses in the absence of TCR engagement.
Fichier non déposé

Dates et versions

hal-00264830 , version 1 (18-03-2008)

Identifiants

  • HAL Id : hal-00264830 , version 1
  • PUBMED : 16670276

Citer

Kevin M Dennehy, Fernando Elias, Gabrielle Zeder-Lutz, Xin Ding, Danièle Altschuh, et al.. Cutting edge: monovalency of CD28 maintains the antigen dependence of T cell costimulatory responses.. Journal of Immunology, 2006, 176 (10), pp.5725-9. ⟨hal-00264830⟩
173 Consultations
0 Téléchargements

Altmetric

Partager

Gmail Facebook X LinkedIn More