| Literature DB >> 33500526 |
Naohito Fujishima1, Junki Kohmaru2, Souichi Koyota2, Keiji Kuba2,3, Tomoo Saga4, Ayumi Omokawa4, Yuki Moritoki4, Shigeharu Ueki4, Fumihiro Ishida5, Shinji Nakao6, Akira Matsuda7, Akiko Ohta8, Kaoru Tohyama9, Hiroshi Yamasaki10, Kensuke Usuki11, Yasuhiro Nakashima12, Shinya Sato13, Yasushi Miyazaki13, Yasuhito Nannya14, Seishi Ogawa14, Kenichi Sawada15, Kinuko Mitani16, Makoto Hirokawa17.
Abstract
Idiopathic pure red cell aplasia (PRCA) and secondary PRCA associated with thymoma and large granular lymphocyte leukemia are generally considered to be immune-mediated. The PRCA2004/2006 study showed that poor responses to immunosuppression and anemia relapse were associated with death. PRCA may represent the prodrome to MDS. Thus, clonal hematopoiesis may be responsible for treatment failure. We investigated gene mutations in myeloid neoplasm-associated genes in acquired PRCA. We identified 21 mutations affecting amino acid sequences in 11 of the 38 adult PRCA patients (28.9%) using stringent filtering of the error-prone sequences and SNPs. Four PRCA patients showed 7 driver mutations in TET2, DNMT3A and KDM6A, and 2 PRCA patients carried multiple mutations in TET2. Five PRCA patients had mutations with high VAFs exceeding 0.3. These results suggest that clonal hematopoiesis by stem/progenitor cells might be related to the pathophysiology of chronic PRCA in certain adult patients.Entities:
Year: 2021 PMID: 33500526 PMCID: PMC7838416 DOI: 10.1038/s41598-021-81890-5
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379