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PMID: 15627212 Published · ppublish English Journal Article

Dendritic cells generated from acute myeloid leukemia (AML) blasts maintain the expression of immunogenic leukemia associated antigens.

Cancer immunology, immunotherapy : CII ·Vol. 54 ·No. 7 ·2005-07-00 ·Pages 685-93

Li L, Reinhardt P, Schmitt A, Barth TF, Greiner J, Ringhoffer M, Döhner H, Wiesneth M, Schmitt M

Abstract

Recently, the focus is on new specific immunotherapies for AML such as cellular therapies employing dendritic cells (DCs) generated from AML blasts. AML-DCs express constitutionally leukemia-associated antigens (LAAs) present in AML blasts they are generated from. Here we investigated whether the generation of AML-DCs would alter the expression level of LAAs. Moreover, we evaluated the presence of HLA and costimulatory molecules on AML blasts versus AML-DCs. Quantitative real-time polymerase chain reaction (PCR) was performed for the following LAAs: preferentially expressed antigen in melanoma (PRAME), the receptor for hyaluronic acid mediated motility (RHAMM/CD168), Wilms' tumor gene 1 (WT-1) and proteinase 3. The expression of HLA-ABC, HLA-DR, CD40, CD80, CD83 and CD86 was evaluated by flow cytometry. RHAMM protein expression was evaluated by immunocytochemistry, recognition of AML-DCs by PRAME epitope-specific T cells was evaluated in a chromium-release assay. Quantitative real-time PCR for AML-DCs versus AML blasts showed an alteration in mRNA expression of LAAs. An elevated PCR signal for PRAME was detected in 7/12 AML-DC preparations. 6/12 AML-DC preparations showed a significant upregulation of the PCR signal for RHAMM. A stronger WT-1 and proteinase-3 signal was observed in PCR for only 2/12 and 1/12 AML-DCs , respectively. All preparations showed a strong expression of at least one of the LAAs examined. As demonstrated by flow cytometry, AML-DCs strongly upregulated costimulatory molecules like CD40 and CD80 in comparison with AML blasts. AML-DCs tested positive for RHAMM protein. PRAME positive AML-DCs were recognized by specific T cells. AML-DCs might constitute a powerful tool in immunotherapy for AML. Real-time PCR allows a quick and quantitative assessment of immunologically relevant LAA expression with only 10(5) DCs and might be helpful for the decision whether the AML-DC vaccination strategy is favourable or not.

MeSH Terms
Acute Disease Antigens, CD/metabolism Antigens, Neoplasm/immunology,metabolism Blast Crisis Cell Survival/immunology Dendritic Cells/immunology Extracellular Matrix Proteins/metabolism HLA-DR Antigens/metabolism Humans Hyaluronan Receptors/metabolism Leukemia, Myeloid/immunology,pathology Myeloblastin RNA, Neoplasm/genetics,metabolism Reverse Transcriptase Polymerase Chain Reaction Serine Endopeptidases/metabolism T-Lymphocytes/immunology,metabolism Tumor Cells, Cultured WT1 Proteins/metabolism
Chemicals
Antigens, CD Antigens, Neoplasm Extracellular Matrix Proteins HLA-DR Antigens Hyaluronan Receptors PRAME protein, human RNA, Neoplasm WT1 Proteins hyaluronan-mediated motility receptor Serine Endopeptidases Myeloblastin
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Li Li
Third Department of Internal Medicine, University of Ulm, Robert-Koch-Street 8, 89081 Ulm, Germany.
Reinhardt Peter
Schmitt Anita
Barth Thomas F E
Greiner Jochen
Ringhoffer Mark
Döhner Hartmut
Wiesneth Markus
Schmitt Michael
Article Info
Journal
Cancer immunology, immunotherapy : CII
Abbr.
Cancer Immunol Immunother
ISSN
0340-7004
Published
2005-07-00
Epub
2004-00-31
Pages
685-93
Language
English
Region
Germany
NLM ID
8605732
Subset
IM
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