Rituximab, B-Lymphocyte Depletion, and Preservation of Beta-Cell Function
Author(s) -
Mark D. Pescovitz,
Carla J. Greenbaum,
Heidi KrauseSteinrauf,
Dorothy J. Becker,
Stephen E. Gitelman,
Robin Goland,
Peter A. Gottlieb,
Jennifer B. Marks,
Paula McGee,
Antoinette Moran,
Philip Raskin,
Henry Rodriguez,
Desmond Schatz,
Diane K. Wherrett,
Darrell M. Wilson,
John M. Lachin,
Jay S. Skyler
Publication year - 2009
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa0904452
Subject(s) - medicine , rituximab , glycated hemoglobin , placebo , gastroenterology , lymphocyte , diabetes mellitus , immunology , cd20 , type 1 diabetes , type 2 diabetes , endocrinology , lymphoma , pathology , alternative medicine
The immunopathogenesis of type 1 diabetes mellitus is associated with T-lymphocyte autoimmunity. However, there is growing evidence that B lymphocytes play a role in many T-lymphocyte-mediated diseases. It is possible to achieve selective depletion of B lymphocytes with rituximab, an anti-CD20 monoclonal antibody. This phase 2 study evaluated the role of B-lymphocyte depletion in patients with type 1 diabetes.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom