Evidence map›Paper›PMID 29740052›Full record

ArticleScientific reports2018

VIPER regulates naive T cell activation and effector responses: Implication in TLR4 associated acute stage T cell responses.

Subhransu Sekhar Sahoo, Belluru M Pratheek, Vikram S Meena, Tapas Kumar Nayak, P Sanjai Kumar, Saumya Bandyopadhyay, Prasanta Kumar Maiti, Subhasis Chattopadhyay

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. 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
0.4field-weighted citation impact, top 41% 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, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
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.

Subhransu Sekhar SahooSchool of Biological Sciences, National Institute of Science Education and Research, HBNI, Bhubaneswar, Jatni, Khurda, 752050, Odisha, India.
Belluru M PratheekSchool of Biological Sciences, National Institute of Science Education and Research, HBNI, Bhubaneswar, Jatni, Khurda, 752050, Odisha, India.
Vikram S MeenaSchool of Biological Sciences, National Institute of Science Education and Research, HBNI, Bhubaneswar, Jatni, Khurda, 752050, Odisha, India.
Tapas Kumar NayakSchool of Biological Sciences, National Institute of Science Education and Research, HBNI, Bhubaneswar, Jatni, Khurda, 752050, Odisha, India.
P Sanjai KumarSchool of Biological Sciences, National Institute of Science Education and Research, HBNI, Bhubaneswar, Jatni, Khurda, 752050, Odisha, India.
Saumya BandyopadhyaySchool of Biological Sciences, National Institute of Science Education and Research, HBNI, Bhubaneswar, Jatni, Khurda, 752050, Odisha, India.
Prasanta Kumar MaitiAbgenex India Pvt Ltd, Bhubaneswar, India.
Subhasis ChattopadhyaySchool of Biological Sciences, National Institute of Science Education and Research, HBNI, Bhubaneswar, Jatni, Khurda, 752050, Odisha, India. subho@niser.ac.in.
National Institute of Science Education and Research · INIMGENEX India (India) · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Naive T cells are known to express the modest level of TLR4 while it is known to go down during TCR activation. However, information towards the requirement of TLR4 signaling during TCR or mitogenic activation of naive wild-type T cells remains scanty. Here we have investigated the endogenous functional expression of TLR4 in naive mice T cells during TCR and mitogenic stimulation in presence of VIPER peptide (VP), an established inhibitor of TLR4 signaling. As expected we found that TLR4 expression goes down during TCR and mitogenic activation. Interestingly, we observed that VP treatment restores TLR4 expression on those activated T cells. Moreover, VP was found to regulate such activation of naive T cell as evident by reduction of CD25, CD69 expression, effector cytokines (IL-2, IFN-γ, TNF) production, T cell proliferation and down-regulation of T cell activation-dependent Fas (CD95), FasL (CD95L) expression. Together, our current observation highlights a possible requirement of TLR4 responses in T cells, which might have possible implication towards the pathogenic acute phase activation of naive T cells.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensCell ProliferationCytokinesFas Ligand ProteinGene Expression RegulationInterleukin-2 Receptor alpha SubunitLectins, C-TypeMiceSignal TransductionT-LymphocytesToll-Like Receptor 4Tumor Necrosis Factor Receptor Superfamily, Member 7Viral ProteinsA46R protein, vaccinia virusAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensCytokinesFas Ligand ProteinInterleukin-2 Receptor alpha SubunitLectins, C-TypeTlr4 protein, mouseToll-Like Receptor 4Tumor Necrosis Factor Receptor Superfamily, Member 7Viral Proteins

Identifiers

PMID29740052
PMCPMC5940837
OpenAlexW2806209828

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.