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The formation of a somatic mutation in the HLA-B gene throughout the development of the disease from severe aplastic anaemia to acute myeloid leukaemia
N. Jana, V. Milena, R. Eva, N. Sara, P. Šárka, Š. Cyril, C. Pietro, B. Jana, B. Monika, DJ. Evangelista,
Jazyk angličtina Země Velká Británie
Typ dokumentu kazuistiky, časopisecké články, práce podpořená grantem
Grantová podpora
MZ ČR - RVO (ÚHKT CZ00023736)
Czech Ministry of Health - International
PubMed
31733047
DOI
10.1111/tan.13762
Knihovny.cz E-zdroje
- MeSH
- akutní myeloidní leukemie genetika patologie MeSH
- aplastická anemie genetika patologie MeSH
- dospělí MeSH
- HLA-B antigeny genetika MeSH
- lidé MeSH
- mutace * MeSH
- myelodysplastické syndromy genetika patologie MeSH
- nádorová transformace buněk genetika MeSH
- progrese nemoci MeSH
- stupeň závažnosti nemoci MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- práce podpořená grantem MeSH
We detected a somatic mutation in the HLA-B gene in a Czech hematooncological patient. We followed the development of this somatic mutation during the transition from severe aplastic anaemia through to myelodysplastic syndrome to acute myeloid leukaemia until haploidentical related transplantation. The somatic mutation differs from HLA-B*14:02 in exon 3 resulting in an exchange from cysteine to serine at position 101 of the mature protein. Homology modelling of mutated S101 in HLA-B*14 indicated possible conformational changes, which might also result in an aberrant expression. The assumption is that somatic mutation arose as a possible result of a selection mediated by a protective immune response against leukaemia.
Institute of Experimental Cellular Therapy University Hospital Essen Essen Germany
Institute of Hematology and Blood Transfusion Hematology and Blood Transfusion Prague Czech Republic
Citace poskytuje Crossref.org
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