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2006 | 53 | 2 | 377-382

Article title

CD40 stimulation induces differentiation of acute lymphoblastic leukemia cells into dendritic cells

Content

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Languages of publication

EN

Abstracts

EN
Despite the very high percentage of long-term remissions in acute lymphoblastic leukemia (ALL) in children, some of them suffer from recurrence of the disease. New treatment modalities, e.g. effective geno- and immunotherapy are needed. The use of neoplasmatic cells to present tumor antigens is one of the approaches in cancer vaccines. ALL cells lack the expression of costimulatory molecules and are poor antigen presenting cells (APCs) for T-cell activation. CD40/40L interaction stimulates B-cells to proliferate, differentiate, upregulate costimulatory molecules and increase antigen presentation. The aim of the study was to test the hypothesis that ALL cells can be turned into professional APCs by CD40L activation. Children with B-cell precursor ALL were enrolled into the study. Mononuclear cells from bone marrow or peripheral blood were stimulated with CD40L and interleukin 4. Results: 1) after culture we noted upregulation of all assessed costimulatory, adhesion and activatory molecules i.e. CD1a, CD11c, CD40, CD54, CD80, CD83, CD86, CD123, HLA class I and II; 2) CD40L activated ALL cells induced proliferation of allogeneic T-cells (measured by [3H]thymidine incorporation). These results confirm the possibility of enhancing the immunogenicity of ALL cells with the CD40L system and indicate that this approach can be used in immunotherapeutic trials.

Year

Volume

53

Issue

2

Pages

377-382

Physical description

Dates

published
2006
received
2005-11-18
revised
2006-03-22
accepted
2006-04-19
(unknown)
2006-05-29

Contributors

  • Department of Pediatric Oncology, Medical University of Białystok, Białystok, Poland
  • Department of Flow Cytometry, Medical University of Białystok, Białystok, Poland
  • Department of Cytogenetics, Medical University of Białystok, Białystok, Poland
  • Department of Pediatric Oncology, Medical University of Białystok, Białystok, Poland
  • Department of Pediatrics, Hematology and Oncology, Medical University of Warsaw, Warsaw, Poland
  • Department of Pediatric Hematology and Oncology, Medical University of Lublin, Lublin, Poland
  • Department of Nuclear Medicine, Medical University of Białystok, Białystok, Poland
  • Students Scientific Section at the Department of Pediatric Oncology, Medical University of Białystok, Białystok, Poland

References

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Publication order reference

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bwmeta1.element.bwnjournal-article-abpv53p377kz
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