Anti-CD3 clinical trials in type 1 diabetes mellitus

Copyright © 2013 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 149(2013), 3 vom: 30. Dez., Seite 268-78
1. Verfasser: Daifotis, Anastasia G (VerfasserIn)
Weitere Verfasser: Koenig, Scott, Chatenoud, Lucienne, Herold, Kevan C
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Review Anti-CD3 Otelixizumab Teplizumab Type 1 diabetes mellitus Antibodies, Monoclonal, Humanized C-Peptide CD3 Complex Hypoglycemic Agents mehr... Insulin Receptors, Fc otelixizumab I5HF2X04PB teplizumab S4M959U2IJ
Beschreibung
Zusammenfassung:Copyright © 2013 Elsevier Inc. All rights reserved.
Two humanized, anti-CD3 mAbs with reduced FcR binding, teplizumab and otelixizumab, have been evaluated in over 1500 subjects, ages 7-45, with new and recently diagnosed T1D with a range of intravenous doses (3-48mg) and regimens (6-14 days, single or repeat courses). In general, studies that used adequate dosing demonstrated improvement in stimulated C-peptide responses and reduced need for exogenous insulin for two years and even longer after diagnosis. Drug treatment causes a transient reduction in circulating T cells, but the available data suggest that the mechanism of action may involve induction of regulatory mechanisms. The adverse effects of anti-CD3 treatment are infusion-related and transient. The studies have identified significant differences in efficacy among patient groups suggesting that a key aspect for development of this immune therapy is identification of the demographic, metabolic, and immunologic features that distinguish subjects who are most likely to show beneficial clinical responses
Beschreibung:Date Completed 30.12.2013
Date Revised 16.11.2017
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2013.05.001