T cell responses are governed by avidity and co-stimulatory thresholds

Détails

ID Serval
serval:BIB_A1B26B4CA778
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
T cell responses are governed by avidity and co-stimulatory thresholds
Périodique
European Journal of Immunology
Auteur⸱e⸱s
Bachmann  M. F., Sebzda  E., Kundig  T. M., Shahinian  A., Speiser  D. E., Mak  T. W., Ohashi  P. S.
ISSN
0014-2980 (Print)
Statut éditorial
Publié
Date de publication
09/1996
Volume
26
Numéro
9
Pages
2017-22
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Sep
Résumé
We analyzed the avidity and CD28-mediated co-stimulatory requirements for the activation of T cells in vivo and in vitro. The strength of the T cell/antigen-presenting cell interaction was varied by using altered peptide ligands for stimulation. Co-stimulatory requirements were studied using T cells from CD28-deficient mice. The results indicate that T cell activation is not an all-or-nothing event, but occurs in distinct steps. For each step, a certain avidity, co-stimulatory threshold or both, must be met. Depending upon the strength of the interaction between the T cell receptor and the major histocompatibility complex/peptide and the presence of CD28 co-stimulatory signals, T cells may undergo blast formation alone or proliferate or eventually both proliferate and differentiate to effector cells. Thus, T cell activation is governed by both avidity and co-stimulatory thresholds.
Mots-clé
Amino Acid Sequence Animals Antigens, CD28/physiology Cytokines/biosynthesis Cytotoxicity, Immunologic Histocompatibility Antigens/physiology Interleukin-2/pharmacology *Lymphocyte Activation Lymphocytic choriomeningitis virus/immunology Mice Mice, Transgenic Molecular Sequence Data Peptide Fragments/immunology Receptors, Antigen, T-Cell/*physiology T-Lymphocytes/*immunology
Pubmed
Web of science
Création de la notice
28/01/2008 12:33
Dernière modification de la notice
20/08/2019 16:07
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