Abstract
B cells play an important role in the pathogenesis of many autoimmune diseases. Different approaches targeting the B cell compartment are under investigation. Selective modulation of B cells has been recently achieved using a humanised monoclonal antibody against the B cell surface marker CD22. This antibody (epratuzumab) was originally developed for the treatment of non-Hodgkin's lymphoma and was found to be effective, with a very good safety profile. Recent studies have demonstrated the efficacy and safety of epratuzumab in several autoimmune diseases, including systemic lupus erythematosus and primary Sjögren's syndrome.
MeSH terms
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Animals
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Antibodies, Monoclonal / administration & dosage
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Antibodies, Monoclonal / therapeutic use*
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Antibodies, Monoclonal, Humanized
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Antineoplastic Agents / administration & dosage
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Antineoplastic Agents / therapeutic use*
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B-Lymphocytes / drug effects
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B-Lymphocytes / immunology
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Drug Administration Schedule
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Drug Interactions
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Drug Therapy, Combination
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Humans
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Lupus Erythematosus, Systemic / drug therapy*
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Lupus Erythematosus, Systemic / immunology
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Lymphoma, Non-Hodgkin / drug therapy*
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Lymphoma, Non-Hodgkin / immunology
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Randomized Controlled Trials as Topic
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Sialic Acid Binding Ig-like Lectin 2 / immunology*
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Sjogren's Syndrome / drug therapy*
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Sjogren's Syndrome / immunology
Substances
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Humanized
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Antineoplastic Agents
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Sialic Acid Binding Ig-like Lectin 2
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epratuzumab