Literature DB >> 7539011

Elimination of B-lineage leukemia and lymphoma cells from bone marrow grafts using anti-B4-blocked-ricin immunotoxin.

D C Roy1, C Perreault, R Bélanger, M Gyger, C Le Houillier, W A Blättler, J M Lambert, J Ritz.   

Abstract

Bone marrow is the primary site of disease in patients with acute lymphoblastic leukemia (ALL) and is frequently involved in patients with non-Hodgkin's lymphoma (NHL). At the time of autologous bone marrow transplantation, marrow grafts from patients with leukemia and lymphoma are often still contaminated by malignant cells, even when such patients achieve complete clinical remission. In this study, we evaluated the potential of anti-B4-blocked-ricin (anti-B4-bR) immunotoxin to eliminate residual ALL and NHL cells from bone marrow. Anti-B4-bR binds to the CD19 antigen, which is B-lineage specific, and, at concentrations of 5 x 10(-9) M or greater, could eliminate more than 3 logs of CD19+ Nalm-6 or Namalwa cells in a 20-fold excess of normal irradiated bone marrow after only 5 hr of incubation. This activity was abrogated by the addition of anti-B4 but not by the presence of galactose, which is the natural ligand for native ricin. Also, when used at these high concentrations, anti-B4-bR showed little nonspecific toxicity against normal hematopoietic progenitors. In conclusion, a single short exposure to anti-B4-bR is capable of inducing high levels of depletion of CD19+ leukemia and lymphoma cells without significant nonspecific toxicity against normal marrow progenitors. Therefore, anti-B4-bR offers an interesting approach to the elimination of B-lineage malignant cells prior to autologous bone marrow transplantation.

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Year:  1995        PMID: 7539011     DOI: 10.1007/bf01489490

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  27 in total

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3.  Culture studies of human pluripotent hemopoietic progenitors.

Authors:  H A Messner; A A Fauser
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4.  Minimal residual disease in childhood B-lineage lymphoblastic leukemia. Persistence of leukemic cells during the first 18 months of treatment.

Authors:  M Yamada; R Wasserman; B Lange; B A Reichard; R B Womer; G Rovera
Journal:  N Engl J Med       Date:  1990-08-16       Impact factor: 91.245

5.  Detection of minimal residual disease in acute lymphoblastic leukemia using immunoglobulin hypervariable region specific oligonucleotide probes.

Authors:  O G Jonsson; R L Kitchens; F C Scott; R G Smith
Journal:  Blood       Date:  1990-11-15       Impact factor: 22.113

6.  Autologous bone marrow transplantation in high-risk remission B-lineage acute lymphoblastic leukemia using a cocktail of three monoclonal antibodies (BA-1/CD24, BA-2/CD9, and BA-3/CD10) plus complement and 4-hydroperoxycyclophosphamide for ex vivo bone marrow purging.

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7.  Radioimmunolocalization of neuroblastoma xenografts with chimeric antibody chCE7.

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8.  Autologous bone marrow transplantation for acute myelocytic leukemia in first remission: a European survey of the role of marrow purging.

Authors:  N C Gorin; P Aegerter; B Auvert; G Meloni; A H Goldstone; A Burnett; A Carella; M Korbling; P Herve; D Maraninchi
Journal:  Blood       Date:  1990-04-15       Impact factor: 22.113

9.  Detection of residual acute lymphoblastic leukemia cells in cultures of bone marrow obtained during remission.

Authors:  Z Estrov; T Grunberger; I D Dubé; Y P Wang; M H Freedman
Journal:  N Engl J Med       Date:  1986-08-28       Impact factor: 91.245

10.  A monoclonal antibody reactive with normal and leukemic human myeloid progenitor cells.

Authors:  J D Griffin; D Linch; K Sabbath; P Larcom; S F Schlossman
Journal:  Leuk Res       Date:  1984       Impact factor: 3.156

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Review 1.  Promising approaches in acute leukemia.

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  1 in total

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