Evidence map›Paper›PMID 38801403›Full record

ArticleJournal of cellular and molecular medicine2024

Unraveling CCL20's role by regulating Th17 cell chemotaxis in experimental autoimmune prostatitis.

Cheng Zhang, Shun Xu, Rui-Jie Hu, Xian-Hong Liu, Shao-Yu Yue, Xiao-Ling Li, Bang-Shun Dai, Chao-Zhao Liang, Chang-Sheng Zhan

Erratum issuedAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Cheng ZhangDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Shun XuDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Rui-Jie HuDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Xian-Hong LiuDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Shao-Yu YueDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Xiao-Ling LiDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Bang-Shun DaiDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Chao-Zhao LiangDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.ORCID 0000-0003-2317-1323
Chang-Sheng ZhanDepartment of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.ORCID 0009-0003-4306-360X

Funding

Anhui Postdoctoral Science Foundation 2008085QH360National Natural Science Foundation of China 82000720National Natural Science Foundation of China 82370776
6 · The paper itself

Abstract

Chronic prostatitis and chronic pelvic pain syndrome (CP/CPPS), a prevalent urological ailment, exerts a profound influence upon the well-being of the males. Autoimmunity driven by Th17 cells has been postulated as a potential factor in CP/CPPS pathogenesis. Nonetheless, elucidating the precise mechanisms governing Th17 cell recruitment to the prostate, triggering inflammation, remained an urgent inquiry. This study illuminated that CCL20 played a pivotal role in attracting Th17 cells to the prostate, thereby contributing to prostatitis development. Furthermore, it identified prostate stromal cells and immune cells as likely sources of CCL20. Additionally, this research unveiled that IL-17A, released by Th17 cells, could stimulate macrophages to produce CCL20 through the NF-κB/MAPK/PI3K pathway. The interplay between IL-17A and CCL20 establishes a positive feedback loop, which might serve as a critical mechanism underpinning the development of chronic prostatitis, thus adding complexity to its treatment challenges.

Indexed as

Autoimmune DiseasesChemokine CCL20ChemotaxisInterleukin-17ProstatitisTh17 CellsAnimalsAutoimmunityDisease Models, AnimalHumansMacrophagesMaleMiceMice, Inbred C57BLNF-kappa BPhosphatidylinositol 3-KinasesCCL20 protein, mouseChemokine CCL20Interleukin-17NF-kappa BPhosphatidylinositol 3-KinasesCCL20/CCR6 axisexperimental autoimmune prostatitisIL‐17AMAPKNF‐κBPI3KTh17

Identifiers

PMID38801403
PMCPMC11129727

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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.