Abstract |
Monoclonal antibodies are a promising new class of therapeutic agents that can be employed to target specific molecules of the immune system or any tissue. They are currently being tested in a number of clinical trials in autoimmune diseases such as multiple sclerosis (MS). One of these, the humanized monoclonal anti-CD25 antibody daclizumab ( Zenapax), is directed against the interleukin-2 (IL-2) receptor alpha chain (CD25) that is involved in clonal expansion of autoreactive T-cells by binding of its ligand IL- 2. Several years ago daclizumab was approved for the prevention of renal allograft rejection. Following promising observations in uveitis, daclizumab has since been tested in a number of small clinical trials in MS based on the rationale that blocking CD25 would prevent the expansion of autoreactive T-lymphocytes. Safety and efficacy data from the preliminary clinical exploration as well as findings about the mechanism of action of anti-CD25 treatment are reviewed here.
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Authors | Dr Sven Schippling, Roland Martin |
Journal | International MS journal
(Int MS J)
Vol. 15
Issue 3
Pg. 94-8
(Sep 2008)
ISSN: 1352-8963 [Print] England |
PMID | 18808743
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
- Antibodies, Monoclonal
- Antibodies, Monoclonal, Humanized
- Immunoglobulin G
- Immunosuppressive Agents
- Interleukin-2 Receptor alpha Subunit
- Daclizumab
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Topics |
- Antibodies, Monoclonal
(adverse effects, therapeutic use)
- Antibodies, Monoclonal, Humanized
- Clinical Trials as Topic
- Daclizumab
- Humans
- Immunoglobulin G
(adverse effects, therapeutic use)
- Immunosuppressive Agents
(adverse effects, therapeutic use)
- Interleukin-2 Receptor alpha Subunit
(antagonists & inhibitors)
- Multiple Sclerosis, Chronic Progressive
(drug therapy)
- Multiple Sclerosis, Relapsing-Remitting
(drug therapy)
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