Abstract
Immunotherapy is promising to improve the prognosis of human leukemias, at least as adjuvant treatment. Tumor-associated antigens such as antigens encoded by MAGE-A1, -A2, -A3, -A4, -A6 and -A12 genes might provide tools in this field. We demonstrated recently that the presentation peptides encoded by MAGE-Agenes might make leukemic blasts suitable targets to cytolytic T lymphocytes. We reported previously negative data of MAGE-A1 gene expression in hematological malignancies, but in further studies positive results of MAGE-A gene expression were published in some subtypes of hematological malignancies such as T leukemia, myeloma and Hodgkin's disease. This led us to enlarge the screening of MAGE-A gene expression in human leukemias. In the RT-PCR screening of a large panel including 154 patients, only weak signal were detected in a few samples. We conclude that MAGE-A genes are not expressed in human leukemias.
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Acknowledgements
We are particularly grateful to Mrs M Swinarska and to Mrs S Landi for excellent technical assistance. We thank Pr AM Capodano and Dr C Brunet for cryopreservation of leukemic cells from childhood leukemias.
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Chambost, H., van Baren, N., Brasseur, F. et al. MAGE-A genes are not expressed in human leukemias. Leukemia 15, 1769–1771 (2001). https://doi.org/10.1038/sj.leu.2402278
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DOI: https://doi.org/10.1038/sj.leu.2402278
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