Evidence map›Paper›PMID 31557129›Full record

ArticleAging2019

CCL28 promotes locomotor recovery after spinal cord injury via recruiting regulatory T cells.

Pengfei Wang, Xiangbei Qi, Guohui Xu, Jianning Liu, Jichao Guo, Xu Li, Xinzhe Ma, Hui Sun

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Regulatory T cells attenuate astrogliosis via IL-10/STAT3/PKC/vimentin signaling and promote neurological recovery after spinal cord injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Bone Marrow-Derived GCAAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  9. Article
  10. Article
  11. Role of regulatory T cells in spinal cord injury.European journal of medical research · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. 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

8 authors at 2 institutions in 1 country.

Pengfei WangDepartment of Neurosurgery, The Third Hospital, Hebei Medical University, Shijiazhuang 050051, China.
Xiangbei QiDepartment of Orthopaedics, The Third Hospital, Hebei Medical University, Shijiazhuang 050051, China.
Guohui XuDepartment of Orthopaedics, The Third Hospital, Hebei Medical University, Shijiazhuang 050051, China.
Jianning LiuDepartment of Orthopaedics, The Third Hospital, Hebei Medical University, Shijiazhuang 050051, China.
Jichao GuoDepartment of Orthopaedics, The Third Hospital, Hebei Medical University, Shijiazhuang 050051, China.
Xu LiDepartment of Orthopaedics, The Third Hospital, Hebei Medical University, Shijiazhuang 050051, China.
Xinzhe MaDepartment of Orthopaedics, The Third Hospital, Hebei Medical University, Shijiazhuang 050051, China.
Hui SunDepartment of Orthopaedics, The Third Hospital, Hebei Medical University, Shijiazhuang 050051, China.
Hebei Medical University · CNThird Hospital of Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChemokines play a key role in post-traumatic inflammation and secondary injury after spinal cord injury (SCI). CCL28, the chemokine CC-chemokine ligand 28, is involved in the epithelial and mucosal immunity. However, whether CCL28 participates in the physiopathologic processes after SCI remains unclear.

resultsCCL28 is upregulated in the spinal cord after SCI. In addition, neutralizing antibodies against IL-1β or TNF-α, or treatment of ML120B, a selective inhibitor of IKK-β, remarkably decrease CCL28 upregulation, suggesting that CCL28 upregulation relies on NF-κB pathway activated by IL-1β and TNF-α after SCI. Moreover, CD4

methodsThe neutralizing antibodies and recombinant CCL28 were injected intraspinally into the mice prior to SCI, which was established via hemitransection. RT-qPCR analysis was performed to determine transcript level, and Western blot analysis and ELISA assay were used to detect protein expression. Immune cells were analyzed by flow cytometry and visualized by immunofluorescence. The chemotaxis was assessed by

conclusionsThese results indicate that NF-κB pathway-regulated CCL28 production plays a protective role after SCI through recruiting CCR10-expressing and immunosuppressive Treg cells, and suggest that interfering CCL28-CCR10 axis might be of potential clinical benefit in improving SCI recovery.

Indexed as

AnimalsAntibodies, NeutralizingChemokines, CCGene Expression RegulationInterleukin-1betaLocomotionMiceNF-kappa BReceptors, CCR10Recombinant ProteinsSpinal Cord InjuriesT-Lymphocytes, RegulatoryTumor Necrosis Factor-alphaUp-RegulationAntibodies, NeutralizingCcl28 protein, mouseCcr10 protein, mouseChemokines, CCInterleukin-1betaNF-kappa BReceptors, CCR10Recombinant ProteinsTumor Necrosis Factor-alphaCCL28CCR10locomotor recoveryregulatory T cellspinal cord injury

Identifiers

PMID31557129
PMCPMC6781990
OpenAlexW2976547402

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.