Evidence map›Paper›PMID 42794682›Full record

ReviewInternational journal of molecular sciences2026

IL-33/ST2 Signaling and Microglial Functional-State Transitions After Spinal Cord Injury: Direct Evidence and Mechanistic Hypotheses.

Ziyu Ma, Zicheng Lu, Zipeng Zhou, Tianhao Wang, Jinhui Zhang, Yifei Ma, Ruihan Niu, Licheng Zhang, Junhao Deng, Yongfei Zhao

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Ziyu MaSenior Department of Orthopedics, Chinese PLA Hospital, Beijing 100853, China.
Zicheng LuSenior Department of Orthopedics, Chinese PLA Hospital, Beijing 100853, China.
Zipeng ZhouSenior Department of Orthopedics, Chinese PLA Hospital, Beijing 100853, China.
Tianhao WangSenior Department of Orthopedics, Chinese PLA Hospital, Beijing 100853, China.
Jinhui ZhangSenior Department of Orthopedics, Chinese PLA Hospital, Beijing 100853, China.
Yifei MaSenior Department of Orthopedics, Chinese PLA Hospital, Beijing 100853, China.
Ruihan NiuSenior Department of Orthopedics, Chinese PLA Hospital, Beijing 100853, China.
Licheng ZhangSenior Department of Orthopedics, Chinese PLA Hospital, Beijing 100853, China.
Junhao DengSenior Department of Orthopedics, Chinese PLA Hospital, Beijing 100853, China.
Yongfei ZhaoSenior Department of Orthopedics, Chinese PLA Hospital, Beijing 100853, China.

Funding

Beijing Natural Science Foundation L248070China Postdoctoral Science Foundation 2025M774434National Natural Science Foundation of China 82272127National Natural Science Foundation of China 82272478National Natural Science Foundation of China 82402786Postdoctoral Research Foundation of China GZC20242291
6 · The paper itself

Abstract

Spinal cord injury (SCI) triggers a complex and evolving cascade of pathological events in which neuroinflammation and microenvironmental imbalance critically constrain repair. Among the cellular mediators, microglia exhibit remarkable functional plasticity, transitioning across diverse states that can either support tissue repair or exacerbate secondary damage. However, the mechanisms governing this dynamic reprogramming remain incompletely understood, limiting the development of effective immunomodulatory strategies. Recent evidence identifies the interleukin-33 (IL-33)/ST2 axis as an emerging, context-dependent regulator linking immune responses to neural repair. Rapidly released as an alarmin following injury, IL-33 modulates microglial function across spatiotemporal dimensions. Here, we propose a two-stage working model integrating direct evidence from SCI with extrapolated insights from broader central nervous system (CNS) pathologies. While acute IL-33 signaling is directly demonstrated in SCI models to limit early neuroinflammation and contain tissue damage, its putative role in driving a subsequent reparative microglial phenotype-encompassing metabolic adaptation and specialized phagocytic clearance-remains a hypothesis largely inferred from brain injury and neurodegenerative paradigms. Furthermore, we explore how IL-33 might modulate intercellular crosstalk with regulatory T cells and astrocytes, emphasizing that these downstream reparative mechanisms require definitive validation within the specific microenvironment of the injured spinal cord. In this Review, we synthesize current advances in the understanding of SCI pathology, microglial heterogeneity, and IL-33-mediated signaling. We highlight how IL-33 integrates inflammatory, metabolic, and transcriptional programs to drive microglial functional reprogramming, and we evaluate emerging therapeutic strategies targeting this pathway. Despite promising preclinical findings, challenges remain in optimizing delivery, timing, and safety. A deeper understanding of the IL-33/ST2 axis and its context-dependent effects may enable precise immunomodulation, offering new avenues to overcome barriers to regeneration and improve functional recovery after SCI.

Indexed as

Interleukin-1 Receptor-Like 1 ProteinInterleukin-33MicrogliaSignal TransductionSpinal Cord InjuriesAnimalsHumansIL1RL1 protein, humanInterleukin-1 Receptor-Like 1 ProteinInterleukin-33IL-33microglial heterogeneityspinal cord injurytissue repair

Identifiers

PMID42794682
PMCPMC13607314

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.