Abstract
Rituximab has been administered successfully in patients with polyneuropathy associated with antibodies to myelin-associated glycoprotein (anti-MAG). The authors present a follow-up study with high-dose rituximab. Increase of rituximab from 375 mg/m2 to a dose of 750 mg/m2 was well tolerated and led to clinical improvement in four of eight patients, along with improvement of nerve conduction velocities and a reduction of anti-MAG antibody titers.
MeSH terms
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Aged
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Antibodies, Monoclonal / adverse effects
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Antibodies, Monoclonal / therapeutic use*
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Antibodies, Monoclonal, Murine-Derived
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Antibody-Dependent Cell Cytotoxicity
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B-Lymphocytes / immunology
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Female
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Follow-Up Studies
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Humans
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Immunoglobulin M / blood
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Immunologic Factors / adverse effects
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Immunologic Factors / therapeutic use*
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Male
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Middle Aged
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Myelin-Associated Glycoprotein / immunology*
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Polyneuropathies / drug therapy*
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Polyneuropathies / immunology*
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Rituximab
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Time Factors
Substances
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Murine-Derived
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Immunoglobulin M
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Immunologic Factors
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Myelin-Associated Glycoprotein
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Rituximab