Evidence map›Paper›PMID 35056114›Full record

ArticlePharmaceuticals (Basel, Switzerland)2022

Presence of TRPA1 Modifies CD4+/CD8+ T Lymphocyte Ratio and Activation.

Katalin Szabó, Ágnes Kemény, Noémi Balázs, Esam Khanfar, Zoltán Sándor, Ferenc Boldizsár, Rolland Gyulai, József Najbauer, Erika Pintér, Tímea Berki

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

10 authors at 1 institution in 1 country.

Katalin SzabóDepartment of Immunology and Biotechnology, University of Pécs Medical School, H-7624 Pécs, Hungary.ORCID 0000-0001-6569-3862
Ágnes KeményDepartment of Pharmacology and Pharmacotherapy, University of Pécs Medical School, H-7624 Pécs, Hungary.ORCID 0000-0002-4523-3938
Noémi BalázsDepartment of Immunology and Biotechnology, University of Pécs Medical School, H-7624 Pécs, Hungary.
Esam KhanfarDepartment of Immunology and Biotechnology, University of Pécs Medical School, H-7624 Pécs, Hungary.ORCID 0000-0001-5260-7937
Zoltán SándorDepartment of Pharmacology and Pharmacotherapy, University of Pécs Medical School, H-7624 Pécs, Hungary.
Ferenc BoldizsárDepartment of Immunology and Biotechnology, University of Pécs Medical School, H-7624 Pécs, Hungary.ORCID 0000-0001-7831-1018
Rolland GyulaiDepartment of Dermatology, Venereology and Oncodermatology, University of Pécs Medical School, H-7624 Pécs, Hungary.ORCID 0000-0002-3286-8846
József NajbauerDepartment of Immunology and Biotechnology, University of Pécs Medical School, H-7624 Pécs, Hungary.
Erika PintérDepartment of Pharmacology and Pharmacotherapy, University of Pécs Medical School, H-7624 Pécs, Hungary.ORCID 0000-0001-9898-632X
Tímea BerkiDepartment of Immunology and Biotechnology, University of Pécs Medical School, H-7624 Pécs, Hungary.ORCID 0000-0002-0134-8127
University of Pecs · HU

Funding

Hungarian Academy of Sciences Ágnes Kemény, János Bolyai Research ScholarshipsMinistry for Innovation and Technology in Hungary NKFIH K_18_128210 Research Grant.Ministry for Innovation and Technology in Hungary NKP-2017-00002 (NAP-2; Chronic Pain Research Group)National Research, Development and Innovation Fund of Hungary 2020-4.1.1-TKP2020National Research, Development and Innovation Fund of Hungary TKP2020-IKA-08
6 · The paper itself

Abstract

Transient Receptor Potential Ankyrin 1 (TRPA1) has been reported to influence neuroinflammation and lymphocyte function. We analysed the immune phenotype and activation characteristics of TRPA1-deficient mice (knockout-KO) generated by targeted deletion of the pore-loop domain of the ion channel. We compared TRPA1 mRNA and protein expression in monocyte and lymphocyte subpopulations isolated from primary and secondary lymphatic organs of wild type (WT) and KO mice. qRT-PCR and flow cytometric studies indicated a higher level of TRPA1 in monocytes than in lymphocytes, but both were orders of magnitude lower than in sensory neurons. We found lower CD4+/CD8+ thymocyte ratios, diminished CD4/CD8 rates, and B cell numbers in the KO mice. Early activation marker CD69 was lower in CD4+ T cells of KO, while the level of CD8+/CD25+ cells was higher. In vitro TcR-mediated activation did not result in significant differences in CD69 level between WT and KO splenocytes, but lower cytokine (IL-1β, IL-6, TNF-α, IL-17A, IL-22, and RANTES) secretion was observed in KO splenocytes. Basal intracellular Ca

Indexed as

B cellsCD4+ cellsCD8+ cellscytokineimiquimodintracellular Ca2+lymphocytesmonocytesmultiparameter flow cytometryqRT-PCRTcR activationTRPA1

Identifiers

PMID35056114
PMCPMC8781558
OpenAlexW4205843874

What OpenQuestion holds

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Registered trials

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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.