Evidence map›Paper›PMID 39900564›Full record

ArticleJournal of cellular and molecular medicine2025

Anti-Inflammatory Resveratrol Protects Mice From Early Mortality After Haematopoietic Stem Cell Transplantation.

Xiao Zhang, Wei Yu, Yimeng Sun, Xinyu Ye, Yu He, Xin Huang, Fuhao Wang, Yi Lu, Jian Zhang

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Xiao ZhangSchool of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong, China.ORCID 0000-0003-1963-2991
Wei YuDepartment of Anesthesiology, the First Affiliated Hospital, Jinan University, Guangzhou, Guangdong, China.
Yimeng SunSchool of Clinical Medicine, Weifang Medical University, Weifang, Shandong, China.
Xinyu YeSchool of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong, China.
Yu HeSchool of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong, China.
Xin HuangSchool of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong, China.
Fuhao WangSchool of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong, China.
Yi LuSchool of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong, China.
Jian ZhangSchool of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong, China.

Funding

National Natural Science Foundation of China NFSC-81972420National Natural Science Foundation of China NFSC-81972766National Natural Science Foundation of China NFSC-82173336Science, Technology and Innovation Commission of Shenzhen Municipality JCYJ20190809161811237Science, Technology and Innovation Commission of Shenzhen Municipality JCYJ20210324104214040
6 · The paper itself

Abstract

The occurrence of inflammation subsequent to haematopoietic stem cell transplantation is associated with an elevated risk of transplant-related mortality (TRM). However, the duration of inflammation and the potential efficacy of anti-inflammatory agents in reducing TRM remain uncertain. We performed a comprehensive investigation to examine the post-transplantation alterations of inflammatory mediators and to ascertain the correlation between inflammation level and TRM through the neutrophil-lymphocyte ratio, ELISAs and cytometric bead array. The findings revealed that the 30-day interval following transplantation is characterised by the most pronounced inflammatory response in both human and murine subjects, thereby elevating the risk of TRM. The inflammation is primarily caused by myeloid bias during haematopoietic reconstitution, which is a commonly overlooked aspect in clinical transplantation, additionally, a lesser extent of irradiation-induced injury. The administration of the anti-inflammatory agent resveratrol has the potential to reduce systemic inflammation and TRM by suppressing the NOD-like receptor signalling pathway and slowing down granulocyte implantation in HSCT mice. This approach did not impair the differentiation potential of haematopoietic stem cells. These findings demonstrate that the 30-day post-transplant period represents an opportunity to facilitate HSCT colonisation, mitigate transplant-related adverse effects, and potentially reap the benefits of anti-inflammatory treatments.

Indexed as

Anti-Inflammatory AgentsHematopoietic Stem Cell TransplantationResveratrolAnimalsFemaleHematopoietic Stem CellsHumansInflammationMaleMiceMice, Inbred C57BLNeutrophilsAnti-Inflammatory AgentsResveratrolhaematopoietic stem cell transplantationinflammationmyeloid biasresveratroltransplant‐related mortality

Identifiers

PMID39900564
PMCPMC11790355

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Registered trials

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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.