Evidence map›Paper›PMID 26462419›Full record

ArticleMucosal immunology2016

Plasmacytoid dendritic cell-derived IFNα modulates Th17 differentiation during early Bordetella pertussis infection in mice.

V Wu, A A Smith, H You, T A Nguyen, R Ferguson, M Taylor, J E Park, P Llontop, K R Youngman, T Abramson

Open access · bronzeAbstract read
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In one paragraph

Article in Mucosal immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Frontiers in immunology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Naturally circulating pertactin-deficientEmerging microbes & infections · 2021
    Article
  9. Review
  10. Age-Dependent Effects of Type I and Type III IFNs in the Pathogenesis ofJournal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Immunity by equilibrium.Nature reviews. Immunology · 2016
    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.

V WuDepartment of Biology, San José State University, San José, California, USA.
A A SmithDepartment of Biology, San José State University, San José, California, USA.
H YouDepartment of Biology, San José State University, San José, California, USA.
T A NguyenDepartment of Biology, San José State University, San José, California, USA.
R FergusonDepartment of Biology, San José State University, San José, California, USA.
M TaylorDepartment of Biology, San José State University, San José, California, USA.
J E ParkDepartment of Biology, San José State University, San José, California, USA.
P LlontopDepartment of Biology, San José State University, San José, California, USA.
K R YoungmanDepartment of Biology, San José State University, San José, California, USA.
T AbramsonDepartment of Biology, San José State University, San José, California, USA.
San Jose State University · US

Funding

Immunodulation by Bordetella Pertussis of Lymphocytes Trafficking to the LungsSC3GM100854 · NIGMS · SAN JOSE STATE UNIVERSITY · PI ABRAMSON, TZVIA · 2012 to 2015
$426k
NIGMS NIH HHS SC3 GM100854
6 · The paper itself

Abstract

Whooping cough is a highly contagious respiratory disease caused by Bordetella pertussis (B. pertussis). T helper 17 (Th17) cells have a central role in the resolution of the infection. Emerging studies document that type I interferons (IFNs) suppress Th17 differentiation and interleukin (IL)-17 responses in models of infection and chronic inflammation. As plasmacytoid dendritic cells (pDCs) are a major source of type I IFNs, we hypothesize that during B. pertussis infection in mice, pDC-derived IFNα inhibits a rapid increase in Th17 cells. We found that IFNα-secreting pDCs appear in the lungs during the early stages of infection, while a robust rise of Th17 cells in the lungs is detected at 15 days post-infection or later. The presence of IFNα led to reduced Th17 differentiation and proliferation in vitro. Furthermore, in vivo blocking of IFNα produced by pDCs during infection with B. pertussis infection resulted in early increase of Th17 frequency, inflammation, and reduced bacterial loads in the airways of infected mice. Taken together, the experiments reported here describe an inhibitory role for pDCs and pDC-derived IFNα in modulating Th17 responses during the early stages of B. pertussis infection, which may explain the prolonged nature of whooping cough.

Indexed as

AnimalsAntibodies, BlockingBacterial LoadBordetella pertussisCell DifferentiationCells, CulturedCoculture TechniquesDendritic CellsFemaleHumansImmunomodulationInterferon-alphaLungLymphocyte ActivationMiceMice, Inbred BALB CAntibodies, BlockingInterferon-alpha

Identifiers

PMID26462419
OpenAlexW119941668

What OpenQuestion holds

Textmetadata
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.