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Dendritic cells generated from acute myeloid leukemia (AML) blasts maintain the expression of immunogenic leukemia associated antigens.
- Source :
-
Cancer immunology, immunotherapy : CII [Cancer Immunol Immunother] 2005 Jul; Vol. 54 (7), pp. 685-93. Date of Electronic Publication: 2004 Dec 31. - Publication Year :
- 2005
-
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.
- Subjects :
- Acute Disease
Antigens, CD metabolism
Antigens, Neoplasm metabolism
Blast Crisis
Cell Survival immunology
Extracellular Matrix Proteins metabolism
HLA-DR Antigens metabolism
Humans
Hyaluronan Receptors metabolism
Leukemia, Myeloid pathology
Myeloblastin
RNA, Neoplasm genetics
RNA, Neoplasm metabolism
Reverse Transcriptase Polymerase Chain Reaction
Serine Endopeptidases metabolism
T-Lymphocytes immunology
T-Lymphocytes metabolism
Tumor Cells, Cultured
WT1 Proteins metabolism
Antigens, Neoplasm immunology
Dendritic Cells immunology
Leukemia, Myeloid immunology
Subjects
Details
- Language :
- English
- ISSN :
- 0340-7004
- Volume :
- 54
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Cancer immunology, immunotherapy : CII
- Publication Type :
- Academic Journal
- Accession number :
- 15627212
- Full Text :
- https://doi.org/10.1007/s00262-004-0631-8