Evidence map›Paper›PMID 41018224›Full record

ArticleVirusdisease2025

MiR-155 and MiR-1275 relation with graft-versus-host disease and hepatitis B in hematopoietic stem cell transplant recipients.

Mani Ramzi, Hossain Ali Rostamipour, Mahdiyar Iravani Saadi, Fakhroddin Hosseini, Zahed Karimi, Zahra Shahhossein, Maryam Ahmadyan

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Article in Virusdisease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Mani RamziHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Hossain Ali RostamipourDepartment of Hematology, Medical Oncology and Stem Cell Transplantation, Shiraz University of Medical Sciences, Shiraz, Iran.
Mahdiyar Iravani SaadiHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID 0000-0002-0104-4684
Fakhroddin HosseiniDepartment of Hematology, Medical Oncology and Stem Cell Transplantation, Shiraz University of Medical Sciences, Shiraz, Iran.
Zahed KarimiDepartment of Hematology, Medical Oncology and Stem Cell Transplantation, Shiraz University of Medical Sciences, Shiraz, Iran.
Zahra ShahhosseinBurn and Wound Healing Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Maryam AhmadyanHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: MicroRNAs (miRNAs) play many roles in basic biological processes such as virus proliferation and growth. In this research, we sought to investigate the prognostic and diagnostic potential of miR-155 and miR-1275 in the induction and severity of Graft-Versus-Host Disease (aGVHD) following hematopoietic stem cell transplantation (HSCT). Additionally, we evaluated the association between these miRNAs' expression and HBV infection in patients with HSCT. Method: In the present research, 135 consecutive patients receiving allogeneic HSCT were enrolled. We assessed the expression levels of miR-155 and miR-1275 in the peripheral blood of patients before and after HSCT by SYBR Green Real-Time PCR. In these patients Hepatitis B virus (HBV) load was also determined by HBV antibody assay. Results: MiR-1275 and miR-155 expression levels were significantly lower in patients after HSCT. A significant association was found between miR-155 and miR-1275 expression levels in patients who developed aGvHD compared with those without aGvHD. We also found that only MiR-155 expression level was significantly increased in HBV + patients compared with HBV- patients. Conclusion: Both MiR-1275 and miR-155 genes have the potential to be used as therapeutic targets in HSCT patients in the future. The expression level of both could be employed as biomarkers for aGvHD induction. Moreover, MiR-155 expression level was connected to the pathogenesis of HBV infection.

Indexed as

aGVHDHematopoietic stem cell transplantationHepatitis B virusMiR-1275MiR-155

Identifiers

PMID41018224
PMCPMC12474801

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.