Document Detail


Anti-Tac (daclizumab, Zenapax) in the treatment of leukemia, autoimmune diseases, and in the prevention of allograft rejection: a 25-year personal odyssey.
MedLine Citation:
PMID:  17216565     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Twenty-five years ago, we reported the production of the monoclonal antibody, anti-Tac that identifies the IL-2 receptor alpha subunit and blocks the interaction of IL-2 with this growth factor receptor. In 1997, daclizumab (Zenapax), the humanized form of this antibody, was approved by the FDA for use in the prevention of renal allograft rejection. In addition, we demonstrated that daclizumab is of value in the treatment of patients with noninfectious uveitis, multiple sclerosis, and the neurological disease human T-cell lymphotropic virus I associated myelopathy/tropical spastic paraparesis (HAM/TSP). Others demonstrated therapeutic efficacy with daclizumab in patients with pure red cell aplasia, aplastic anemia, and psoriasis. Thus, translation of basic insights concerning the IL-2/IL-2 receptor system obtained using the monoclonal antibody daclizumab provided a useful strategy for the prevention of organ allograft rejection and the treatment of patients with select autoimmune diseases or T-cell leukemia/lymphoma.
Authors:
Thomas A Waldmann
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Intramural; Review     Date:  2007-01-11
Journal Detail:
Title:  Journal of clinical immunology     Volume:  27     ISSN:  0271-9142     ISO Abbreviation:  J. Clin. Immunol.     Publication Date:  2007 Jan 
Date Detail:
Created Date:  2007-02-08     Completed Date:  2007-05-08     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  8102137     Medline TA:  J Clin Immunol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1-18     Citation Subset:  IM    
Affiliation:
Metabolism Branch, Center for Cancer Research, National Cancer Institute, NIH Building 10, Bethesda, Maryland 20892-1374, USA. tawald@helix.nih.gov
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MeSH Terms
Descriptor/Qualifier:
Animals
Antibodies, Monoclonal / immunology,  pharmacology,  therapeutic use*
Autoimmune Diseases / drug therapy*
Binding, Competitive / immunology
Graft Rejection / immunology,  prevention & control*
Humans
Immunoglobulin G / immunology,  pharmacology,  therapeutic use*
Immunosuppressive Agents / therapeutic use*
Interleukin-2 / antagonists & inhibitors,  immunology
Interleukin-2 Receptor alpha Subunit / antagonists & inhibitors,  immunology
Leukemia / drug therapy*,  metabolism
Leukemia-Lymphoma, Adult T-Cell / drug therapy
Mice
Paraparesis, Tropical Spastic / drug therapy
Receptors, Interleukin-2 / antagonists & inhibitors,  drug effects*,  immunology
Uveitis / drug therapy
Chemical
Reg. No./Substance:
0/Antibodies, Monoclonal; 0/Immunoglobulin G; 0/Immunosuppressive Agents; 0/Interleukin-2; 0/Interleukin-2 Receptor alpha Subunit; 0/Receptors, Interleukin-2; 152923-56-3/daclizumab

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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