Detailed Information on Publication Record
2018
Association of HLA class I type with prevalence and outcome of patients with acute myeloid leukemia and mutated nucleophosmin
KUZELOVA, Katerina, Barbora BRODSKA, Johannes SCHETELIG, Christoph ROLLING, Zdeněk RÁČIL et. al.Basic information
Original name
Association of HLA class I type with prevalence and outcome of patients with acute myeloid leukemia and mutated nucleophosmin
Authors
KUZELOVA, Katerina (203 Czech Republic, guarantor), Barbora BRODSKA (203 Czech Republic), Johannes SCHETELIG (276 Germany), Christoph ROLLING (276 Germany), Zdeněk RÁČIL (203 Czech Republic, belonging to the institution), Juliane Stickel WALZ (276 Germany), Grzegorz HELBIG (616 Poland), Ota FUCHS (203 Czech Republic), Milena VRANA (203 Czech Republic), Pavla PECHERKOVA (203 Czech Republic), Cyril SALEK (203 Czech Republic) and Jiří MAYER (203 Czech Republic, belonging to the institution)
Edition
Plos one, San Francisco, Public Library of Science, 2018, 1932-6203
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30204 Oncology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 2.776
RIV identification code
RIV/00216224:14110/18:00106958
Organization unit
Faculty of Medicine
UT WoS
000453451000008
Keywords in English
Acute myeloid leukemia
Tags
International impact, Reviewed
Změněno: 9/2/2019 20:46, Soňa Böhmová
Abstract
V originále
Acute myeloid leukemia with mutated nucleophosmin (NPMc+AML) forms a distinct AML subgroup with better prognosis which can potentially be associated with immune response against the mutated nucleophosmin (NPM). As the T-cell-mediated immunity involves antigen presentation on HLA class I molecules, we hypothesized that individuals with suitable HLA type could be less prone to develop NPMc+AML. We compared HLA class I distribution in NPMc+AML patient cohort (398 patients from 5 centers) with the HLA allele frequencies of the healthy population and found HLA-A*02, B*07, B*40 and C*07 underrepresented in the NPMc+AML group. Presence of B*07 or C*07:01 antigen was associated with better survival in patients without concomitant FLT3 internal tandem duplication. Candidate NPM-derived immunopeptides were found for B*40 and B*07 using prediction software tools. Our findings suggest that a T-cell-mediated immune response could actually explain better prognosis of NPMc+ patients and provide a rationale for attempts to explore the importance of immunosuppressive mechanisms in this AML subgroup.
Links
NV15-25809A, research and development project |
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