Evidence map›Paper›PMID 35432343›Full record

ArticleFrontiers in immunology2022

IL-33/ST2 Axis Protects Against Traumatic Brain Injury Through Enhancing the Function of Regulatory T Cells.

Di Xie, Wanying Miao, Fei Xu, Chunling Yuan, Sicheng Li, Chujun Wang, Aditi Junagade, Xiaoming Hu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 4% of its field
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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  4. Targeting IL-33 in Precision Neuroimmunology: Cellular Mechanisms and Therapeutic Strategies for CNS Disorders.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
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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

8 authors at 2 institutions in 1 country.

Di XieDepartment of Neurology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Wanying MiaoDepartment of Neurology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Fei XuDepartment of Neurology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Chunling YuanDepartment of Neurology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Sicheng LiDepartment of Neurology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Chujun WangDepartment of Neurology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Aditi JunagadeDepartment of Neurology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Xiaoming HuDepartment of Neurology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
University of Pittsburgh · USGeriatric Research Education and Clinical Center · US

Funding

Interleukin-33 as an immune therapy for strokeI01BX003651 · VA · VETERANS HEALTH ADMINISTRATION · PI HU, XIAOMING · 2019 to 2023
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BLRD VA I01 BX003651BLRD VA I01 BX005589
6 · The paper itself

Abstract

Traumatic brain injury (TBI) is a devastating condition due to its long-term sequelae on neurological functions. Inflammatory responses after TBI are critical for injury expansion and repair. Recent research in central nervous system (CNS) disorders reveals the importance of IL-33 and its receptor (ST2) as an alarmin system to initiate immune responses. This study explored the role of IL-33/ST2 signaling in TBI. TBI was induced in adult male C57BL/6J mice using a controlled cortical impact (CCI) model. We found that the expression of IL-33 increased in the injured brain and blood, and ST2 was elevated in the circulating and infiltrating regulatory T cells (Tregs) early after TBI. ST2 deficient mice exhibited reduced Treg numbers in the blood and brain 5 days after TBI. The brain lesion size was enlarged in ST2 knockout mice, which was accompanied by deteriorated sensorimotor function 5 days after TBI. In contrast, post-TBI treatment with IL-33 (2 μg/30 g body weight, intranasal) for 3 days significantly reduced brain lesion size and improved neurological functions 5 days after TBI. Meanwhile, IL-33 treatment increased ST2 expression in circulating and brain infiltrating Tregs. To further explore the involvement of Tregs in IL-33/ST2-mediated neuroprotection, Tregs were depleted by CD25 antibody injection. The absence of Tregs significantly reduced the protective effect of IL-33 after TBI.

Indexed as

Brain Injuries, TraumaticInterleukin-33AnimalsInterleukin-1 Receptor-Like 1 ProteinMaleMiceMice, Inbred C57BLT-Lymphocytes, RegulatoryInterleukin-1 Receptor-Like 1 ProteinInterleukin-33IL-33neuroprotectionregulatory T cellsST2traumatic brain injury

Identifiers

PMID35432343
PMCPMC9006950
OpenAlexW4220926622

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.