Evidence map›Paper›PMID 27913566›Full record

ArticleThe Journal of experimental medicine2017

Th2 responses are primed by skin dendritic cells with distinct transcriptional profiles.

Lisa M Connor, Shiau-Choot Tang, Emmanuelle Cognard, Sotaro Ochiai, Kerry L Hilligan, Samuel I Old, Christophe Pellefigues, Ruby F White, Deepa Patel, Adam Alexander T Smith and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

49 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
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  15. Atopic Dermatitis: The Fate of the Fat.International journal of molecular sciences · 2022
    Review
  16. Review
  17. Article
  18. Article
  19. Contact dermatitis.Nature reviews. Disease primers · 2021
    Review
  20. Diverse innate stimuli activate basophils through pathways involving Syk and IκB kinases.Proceedings of the National Academy of Sciences of the United States of America · 2021
    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

14 authors at 3 institutions in 1 country.

Lisa M ConnorMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Shiau-Choot TangMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Emmanuelle CognardMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Sotaro OchiaiMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Kerry L HilliganMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Samuel I OldMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Christophe PellefiguesMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Ruby F WhiteMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Deepa PatelMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Adam Alexander T SmithMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
David A EcclesMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Olivier LamiableMalaghan Institute of Medical Research, Wellington 6012, New Zealand.
Melanie J McConnellSchool of Biological Sciences, Victoria University of Wellington, Wellington 6012, New Zealand.
Franca RoncheseMalaghan Institute of Medical Research, Wellington 6012, New Zealand fronchese@malaghan.org.nz.
Malaghan Institute of Medical Research · NZUniversity of Otago · NZVictoria University of Wellington · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The dendritic cell signals required for the in vivo priming of IL-4-producing T cells are unknown. We used RNA sequencing to characterize DCs from skin LN of mice exposed to two different Th2 stimuli: the helminth parasite Nippostrongylus brasiliensis (Nb) and the contact sensitizer dibutyl phthalate (DBP)-FITC. Both Nb and DBP-FITC induced extensive transcriptional changes that involved multiple DC subsets. Surprisingly, these transcriptional changes were highly distinct in the two models, with only a small number of genes being similarly regulated in both conditions. Pathway analysis of expressed genes identified no shared pathways between Nb and DBP-FITC, but revealed a type-I IFN (IFN-I) signature unique to DCs from Nb-primed mice. Blocking the IFN-I receptor at the time of Nb treatment had little effect on DC migration and antigen transport to the LN, but inhibited the up-regulation of IFN-I-induced markers on DCs and effectively blunted Th2 development. In contrast, the response to DBP-FITC was not affected by IFN-I receptor blockade, a finding consistent with the known dependence of this response on the innate cytokine TSLP. Thus, the priming of Th2 responses is associated with distinct transcriptional signatures in DCs in vivo, reflecting the diverse environments in which Th2 immune responses are initiated.

Indexed as

AnimalsDendritic CellsImmunoglobulinsInterferon Type IMiceMice, Inbred C57BLNippostrongylusReceptor, Interferon alpha-betaReceptors, CytokineSkinTh2 CellsTranscription, GeneticIfnar1 protein, mouseImmunoglobulinsInterferon Type IReceptor, Interferon alpha-betaReceptors, CytokineTslpr protein, mouse

Identifiers

PMID27913566
PMCPMC5206495
OpenAlexW2559535985

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.