Demonstration of highly specific toxicity of the alpha-emitting radioimmunoconjugate(211)At-rituximab against non-Hodgkin's lymphoma cells.

E Aurlien, R H Larsen, G Kvalheim, O S Bruland
Author Information
  1. E Aurlien: Department of Oncology, The Norwegian Radium Hospital, Montebello, Oslo, N-0310, USA.

Abstract

The ability of an alpha-emitter conjugated to a chimaeric anti-CD20 monoclonal antibody to kill selectively human B-lymphoma cells in vitro is reported. Two B-lymphoma cell lines RAEL and K422, and normal haematopoietic progenitor cells from human bone marrow aspirates were incubated with(211)At-rituximab (Rituxan(R) or MabTheratrade mark) and plated in clonogenic assays for survival analyses. Following 1 h incubation with(211)At-rituximab, in concentrations which gave an initial activity of 50 kBq ml(-1), a high tumour cell to normal bone marrow cell toxicity ratio was obtained; 4.1 to 1.0 log cell kill. Biodistribution studies of(211)At-rituximab in Balb/c mice showed similar stability as that of the iodinated analogue. The data indicate that testing of(211)At-rituximab in human patients is warranted.

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MeSH Term

Antibodies, Monoclonal
Antibodies, Monoclonal, Murine-Derived
Antineoplastic Agents
Astatine
Cell Death
Cell Survival
Hematopoietic Stem Cells
Humans
Immunoconjugates
Lymphoma, Non-Hodgkin
Radioisotopes
Rituximab
Tumor Cells, Cultured

Chemicals

Antibodies, Monoclonal
Antibodies, Monoclonal, Murine-Derived
Antineoplastic Agents
Immunoconjugates
Radioisotopes
Rituximab
Astatine

Word Cloud

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