Evidence map›Paper›PMID 27265209›Full record

ArticleScientific reports2016

Triggering through NOD-2 Differentiates Bone Marrow Precursors to Dendritic Cells with Potent Bactericidal activity.

Nargis Khan, Mohammad Aqdas, Aurobind Vidyarthi, Shikha Negi, Susanta Pahari, Tapan Agnihotri, Javed N Agrewala

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Cumulative Signaling Through NOD-2 and TLR-4 Eliminates theFrontiers in cellular and infection microbiology · 2021
    Article
  4. Review
  5. Article
  6. 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

7 authors at 1 institution in 1 country.

Nargis KhanCSIR-Institute of Microbial Technology, Chandigarh, 160036, INDIA.
Mohammad AqdasCSIR-Institute of Microbial Technology, Chandigarh, 160036, INDIA.
Aurobind VidyarthiCSIR-Institute of Microbial Technology, Chandigarh, 160036, INDIA.
Shikha NegiCSIR-Institute of Microbial Technology, Chandigarh, 160036, INDIA.
Susanta PahariCSIR-Institute of Microbial Technology, Chandigarh, 160036, INDIA.
Tapan AgnihotriCSIR-Institute of Microbial Technology, Chandigarh, 160036, INDIA.
Javed N AgrewalaCSIR-Institute of Microbial Technology, Chandigarh, 160036, INDIA.
Institute of Microbial Technology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) play a crucial role in bridging innate and adaptive immunity by activating naïve T cells. The role of pattern recognition receptors like Toll-Like Receptors and Nod-Like Receptors expressed on DCs is well-defined in the recognition of the pathogens. However, nothing is precisely studied regarding the impact of NOD-2 signaling during the differentiation of DCs. Consequently, we explored the role of NOD-2 signaling in the differentiation of DCs and therefore their capability to activate innate and adaptive immunity. Intriguingly, we observed that NOD-2 stimulated DCs (nDCs) acquired highly activated and matured phenotype and exhibited substantially greater bactericidal activity by robust production of nitric oxide. The mechanism involved in improving the functionality of nDCs was dependent on IFN-αβ signaling, leading to the activation of STAT pathways. Furthermore, we also observed that STAT-1 and STAT-4 dependent maturation and activation of DCs was under the feedback mechanism of SOCS-1 and SOCS-3 proteins. nDCs acquired enhanced potential to activate chiefly Th1 and Th17 immunity. Taken together, these results suggest that nDCs can be exploited as an immunotherapeutic agent in bolstering host immunity and imparting protection against the pathogens.

Indexed as

Adaptive ImmunityAnimalsBone Marrow CellsCell DifferentiationCells, CulturedDendritic CellsImmunity, InnateInterferon-alphaInterferon-betaMiceMycobacteriumNod2 Signaling Adaptor ProteinSignal TransductionSTAT Transcription FactorsTh17 CellsTh1 CellsInterferon-alphaInterferon-betaNod2 protein, mouseNod2 Signaling Adaptor ProteinSTAT Transcription Factors

Identifiers

PMID27265209
PMCPMC4893688
OpenAlexW2417323792

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.