Evidence map›Paper›PMID 34473953›Full record

ArticleNeuron2021

IL-23/IL-17A/TRPV1 axis produces mechanical pain via macrophage-sensory neuron crosstalk in female mice.

Xin Luo, Ouyang Chen, Zilong Wang, Sangsu Bang, Jasmine Ji, Sang Hoon Lee, Yul Huh, Kenta Furutani, Qianru He, Xueshu Tao and 7 more

Open access · greenAbstract read
In one paragraph

Article in Neuron, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed, 1 pooled it
16.1field-weighted citation impact, top 1% 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

116 citing papers in PubMed, 1 synthesis or guideline pooled it, 189 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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  5. Article
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  7. Article
  8. CD4The journal of headache and pain · 2026
    Article
  9. Review
  10. Article
  11. A novel role for TRPV1 in macrophage giant cell formation.bioRxiv : the preprint server for biology · 2026
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
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  18. Article
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56 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Xin LuoCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA. Electronic address: xin.luo21@hotmail.com.
Ouyang ChenCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA; Department of Cell Biology, Duke University Medical Center, Durham, NC, USA.
Zilong WangCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Sangsu BangCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Jasmine JiCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Sang Hoon LeePain Research Center, Department of Anesthesiology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Yul HuhCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA; Department of Cell Biology, Duke University Medical Center, Durham, NC, USA.
Kenta FurutaniCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Qianru HeCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Xueshu TaoCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Mei-Chuan KoDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Andrey BortsovCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Christopher R DonnellyCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Yong ChenDepartment of Neurology, Duke University Medical Center, Durham, NC, USA.
Andrea NackleyCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA; Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, USA.
Temugin BertaPain Research Center, Department of Anesthesiology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Ru-Rong JiCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA; Department of Cell Biology, Duke University Medical Center, Durham, NC, USA; Department of Neurobiology, Duke University Medical Center, Durham, NC, USA. Electronic address: ru-rong.ji@duke.edu.
Duke Medical Center · USDuke University Hospital · USUniversity of Cincinnati Medical Center · USWake Forest University · US

Funding

INTEGRATED TRAINING IN ANESTHESIOLOGY RESEARCHT32GM008600 · NIGMS · DUKE UNIVERSITY · PI Miriam Treggiari · 1996 to 2026
$6.6M
Sexual dimorphism of neuroimmune interactions in temporomandibular joint disorders pain: contribution of a newly identified female-specific pain signaling axis IL23/IL17A/TRPV1R01DE027454 · NIDCR · DUKE UNIVERSITY · PI CHEN, YONG · 2018 to 2022
$2.7M
Targeting sensory ganglia and glial signaling for the treatment of acute and chronic painR01NS113243 · NINDS · UNIVERSITY OF CINCINNATI · PI BERTA, TEMUGIN · 2019 to 2019
$2.0M
Spinal BNP-NPRA Signaling in Regulating Itch and Pain in PrimatesR21AR069861 · NIAMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KO, MEI-CHUAN · 2018 to 2019
$375k
NIAMS NIH HHS R21 AR069861NIDCR NIH HHS R01 DE027454NIGMS NIH HHS T32 GM008600NINDS NIH HHS R01 NS113243
6 · The paper itself

Abstract

Although sex dimorphism is increasingly recognized as an important factor in pain, female-specific pain signaling is not well studied. Here we report that administration of IL-23 produces mechanical pain (mechanical allodynia) in female but not male mice, and chemotherapy-induced mechanical pain is selectively impaired in female mice lacking Il23 or Il23r. IL-23-induced pain is promoted by estrogen but suppressed by androgen, suggesting an involvement of sex hormones. IL-23 requires C-fiber nociceptors and TRPV1 to produce pain but does not directly activate nociceptor neurons. Notably, IL-23 requires IL-17A release from macrophages to evoke mechanical pain in females. Low-dose IL-17A directly activates nociceptors and induces mechanical pain only in females. Finally, deletion of estrogen receptor subunit α (ERα) in TRPV1

Indexed as

AnimalsCells, CulturedEstrogen Receptor alphaFemaleHumansInterleukin-17Interleukin-23MacrophagesMaleMiceMice, Inbred C57BLNerve Fibers, UnmyelinatedNociceptive PainNociceptorsSex FactorsSignal TransductionEstrogen Receptor alphaInterleukin-17Interleukin-23TRPV1 protein, mouseTRPV Cation Channelsdorsal root ganglionestrogen receptor αhumanIL-17IL-23macrophagemechanical allodynianociceptornonhuman primatesex dimorphism

Identifiers

PMID34473953
PMCPMC8425601
OpenAlexW3184174289

What OpenQuestion holds

Textmetadata
LicenceTDM
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.