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Lookup NU author(s): Dr Rachel CrosslandORCiD
This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).
© 2025 The Authors. Published by Elsevier Inc. on behalf of American Society for Histocompatibility and Immunogenetics. This is an open access article under the CC BY-NC license. http://creativecommons.org/licenses/by-nc/4.0/Cytomegalovirus (CMV) reactivation is a common complication after allogeneic haematopoietic stem cell transplantation (HSCT). It occurs in over a third of alloHSCT recipients, and is a major source of post-transplant mortality. miRNAs are small non-coding RNA molecules that are important regulators of gene expression. They are often dysregulated during disease, including transplant-related complications. Due to their presence in all body fluids, they can be used as potential biomarkers. In this study, we performed miRNA profiling to find differentially expressed host miRNAs in serum that could be linked to CMV reactivation after HSCT. CMV reactivation was confirmed by detection of CMV DNA in serum. We identified two miRNAs, miR-302d-3p (p < 0.001) and miR-6721-5p (p = 0.018), as differentially expressed between day + 30 and + 90 after HSCT in patients with CMV reactivation. Of these, miR-302d-3p was confirmed as overexpressed on day + 30 in a verification analysis performed on an independent cohort of patients (p = 0.027). Furthermore, we analysed two genetic variants in the gene coding for miR-302d-3p. We found one of them, rs13136737, to be significantly associated with CMV reactivation (p = 0.015). In conclusion, our study showed that miR-302d-3p is dysregulated and that its genetic variant rs13136737 may be important in development of CMV reactivation after HSCT.
Author(s): Lacina P, Crossland RE, Siemaszko J, Szeremet A, Majcherek M, Czyz A, Sobczyk-Kruszelnicka M, Fidyk W, Solarska I, Nasilowska-Adamska B, Skowronska P, Bieniaszewska M, Tomaszewska A, Basak GW, Giebel S, Wrobel T, Bogunia-Kubik K
Publication type: Article
Publication status: Published
Journal: Human Immunology
Year: 2025
Volume: 86
Issue: 6
Print publication date: 01/11/2025
Online publication date: 08/10/2025
Acceptance date: 24/09/2025
Date deposited: 03/11/2025
ISSN (print): 0198-8859
ISSN (electronic): 1879-1166
Publisher: Elsevier Inc.
URL: https://doi.org/10.1016/j.humimm.2025.111599
DOI: 10.1016/j.humimm.2025.111599
PubMed id: 41067185
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