Evidence map›Paper›PMID 26700618›Full record

ArticleOncotarget2016

The role of TRPV1 in the CD4+ T cell-mediated inflammatory response of allergic rhinitis.

Ramachandran Samivel, Dae Woo Kim, Hye Ran Son, Yun-Hee Rhee, Eun Hee Kim, Ji Hye Kim, Jun-Sang Bae, Young-Jun Chung, Phil-Sang Chung, Eyal Raz and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Article
  3. TRPV1: The key bridge in neuroimmune interactions.Journal of intensive medicine · 2024
    Review
  4. Evaluation ofMolecules (Basel, Switzerland) · 2024
    Article
  5. Review
  6. Review
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  8. Review
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  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Calcium signalling in T cells.Nature reviews. Immunology · 2019
    Review
  19. Review
  20. 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

11 authors at 3 institutions in 2 countries.

Ramachandran SamivelDepartment of Otorhinolaryngology, Dankook University College of Medicine, Cheonan, South Korea.
Dae Woo KimDepartment of Otorhinolaryngology-Head and Neck Surgery, Boramae Medical Center, Seoul National University College of Medicine, Seoul, South Korea.
Hye Ran SonDepartment of Otorhinolaryngology, Dankook University College of Medicine, Cheonan, South Korea.
Yun-Hee RheeBeckman Laser Institute Korea, Dankook University College of Medicine, Cheonan, South Korea.
Eun Hee KimDepartment of Otorhinolaryngology, Dankook University College of Medicine, Cheonan, South Korea.
Ji Hye KimDepartment of Otorhinolaryngology, Dankook University College of Medicine, Cheonan, South Korea.
Jun-Sang BaeBeckman Laser Institute Korea, Dankook University College of Medicine, Cheonan, South Korea.
Young-Jun ChungDepartment of Otorhinolaryngology, Dankook University College of Medicine, Cheonan, South Korea.
Phil-Sang ChungDepartment of Otorhinolaryngology, Dankook University College of Medicine, Cheonan, South Korea.
Eyal RazDepartment of Medicine, University of California, San Diego, La Jolla, California, USA.
Ji-Hun MoDepartment of Otorhinolaryngology, Dankook University College of Medicine, Cheonan, South Korea.
Dankook University · KRSNUH SMG-SNU Boramae Medical Center · KRUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transient receptor potential vanilloid 1 (TRPV1), which has been identified as a molecular target for the activation of sensory neurons by various painful stimuli, was reported to regulate the signaling and activation of CD4+ T cells. However, the role of TRPV1 in CD4+ T cell in allergic rhinitis remains poorly understood. In this study, TRPV1 expression was localized in CD4+ T cells. Both knockout and chemical inhibition of TRPV1 suppressed Th2/Th17 cytokine production in CD4 T cells and Jurkat T cells, respectively, and can suppress T cell receptor signaling pathways including NF-κB, MAP kinase, and NFAT. In TRPV1 knockout allergic rhinitis (AR) mice, eosinophil infiltration, Th2/Th17 cytokines in the nasal mucosa, and total and ova-specific IgE levels in serum decreased, compared with wild-type AR mice. The TRPV1 antagonists, BCTC or theobromine, showed similar inhibitory immunologic effects on AR mice models. In addition, the number of TRPV1+/CD4+ inflammatory cells increased in the nasal mucosa of patients with AR, compared with that of control subjects. Thus, TRPV1 activation on CD4+ T cells is involved in T cell receptor signaling, and it could be a novel therapeutic target in AR.

Indexed as

AdolescentAdultAnimalsBlotting, WesternCD4-Positive T-LymphocytesCytokinesEosinophilsFemaleHumansImmunoglobulin EImmunohistochemistryInflammationJurkat CellsMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutCytokinesImmunoglobulin EOvalbuminTRPV Cation Channelsallergic rhinitisBCTCCD4 T lymphocyteImmune responseImmunityImmunology and Microbiology SectionOVATRPV1

Identifiers

PMID26700618
PMCPMC4807989
OpenAlexW2213898944

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.