IL-2/anti-IL-2 antibody complexes show strong biological activity by avoiding interaction with IL-2 receptor alpha subunit CD25.

Détails

ID Serval
serval:BIB_72BA2B267468
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
IL-2/anti-IL-2 antibody complexes show strong biological activity by avoiding interaction with IL-2 receptor alpha subunit CD25.
Périodique
Proceedings of the National Academy of Sciences of the United States of America
Auteur⸱e⸱s
Létourneau S., van Leeuwen E.M., Krieg C., Martin C., Pantaleo G., Sprent J., Surh C.D., Boyman O.
ISSN
1091-6490 (Electronic)
ISSN-L
0027-8424
Statut éditorial
Publié
Date de publication
2010
Volume
107
Numéro
5
Pages
2171-2176
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
IL-2 is crucial to T cell homeostasis, especially of CD4(+) T regulatory cells and memory CD8(+) cells, as evidenced by vigorous proliferation of these cells in vivo following injections of superagonist IL-2/anti-IL-2 antibody complexes. The mechanism of IL-2/anti-IL-2 antibody complexes is unknown owing to a lack of understanding of IL-2 homeostasis. We show that IL-2 receptor alpha (CD25) plays a crucial role in IL-2 homeostasis. Thus, prolongation of IL-2 half-life and blocking of CD25 using antibodies or CD25-deficient mice led in combination, but not alone, to vigorous IL-2-mediated T cell proliferation, similar to IL-2/anti-IL-2 antibody complexes. These data suggest an unpredicted role for CD25 in IL-2 homeostasis.
Mots-clé
Animals, Antibodies, Blocking/administration & dosage, Antigen-Antibody Complex/metabolism, Half-Life, Homeostasis, Immunoglobulin G/metabolism, Interleukin-2/immunology, Interleukin-2/metabolism, Interleukin-2 Receptor alpha Subunit/antagonists & inhibitors, Interleukin-2 Receptor alpha Subunit/deficiency, Mice, Mice, Congenic, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Receptors, Fc/metabolism, Recombinant Fusion Proteins/immunology, Recombinant Fusion Proteins/metabolism
Pubmed
Web of science
Open Access
Oui
Création de la notice
23/02/2010 15:58
Dernière modification de la notice
20/08/2019 15:30
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