Abstract
The mechanism of action of alemtuzumab (CAMPATH 1H) in chronic lymphocytic leukemia (CLL) is uncertain. We tested the hypothesis that alemtuzumab alone can induce apoptosis in cultured CLL cells. Purified peripheral blood B-lymphocytes from CLL patients were treated in serum free medium (AIM-V). There was minimal spontaneous apoptosis in untreated cells. Alemtuzumab ligation did not alter the membrane distribution of CD52 in single cells but many cells formed transient, small, tightly adherent clusters. Alemtuzumab alone did not induce apoptosis. In contrast, alemtuzumab plus complement was rapidly cytotoxic. We conclude that alemtuzumab does not cause apoptosis in purified CLL B cells cultured in serum free medium.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Alemtuzumab
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Antibodies, Monoclonal / pharmacology*
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Antibodies, Monoclonal, Humanized
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Antibodies, Neoplasm / pharmacology*
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Antineoplastic Agents / pharmacology*
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Apoptosis / drug effects*
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Cell Line, Tumor
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Chlorambucil / pharmacology
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Complement System Proteins / physiology
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Culture Media, Serum-Free
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Humans
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Immunoglobulin Fab Fragments / pharmacology
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Leukemia, Lymphocytic, Chronic, B-Cell / drug therapy*
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Leukemia, Lymphocytic, Chronic, B-Cell / pathology
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Vidarabine / analogs & derivatives*
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Vidarabine / pharmacology
Substances
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Humanized
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Antibodies, Neoplasm
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Antineoplastic Agents
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Culture Media, Serum-Free
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Immunoglobulin Fab Fragments
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Chlorambucil
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Alemtuzumab
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Complement System Proteins
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Vidarabine
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fludarabine