Evidence map›Paper›PMID 27014268›Full record

ArticleFrontiers in immunology2016

TLR3 Signaling Promotes the Induction of Unique Human BDCA-3 Dendritic Cell Populations.

Nicholas J Colletti, Hong Liu, Adam C Gower, Yuriy O Alekseyev, Christopher W Arendt, Michael H Shaw

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. The Biology of Dendritic Cells: In Health and Disease.Advances in experimental medicine and biology · 2025
    Review
  3. Review
  4. Molluscum Contagiosum Virus: Biology and Immune Response.Advances in experimental medicine and biology · 2024
    Review
  5. Article
  6. Review
  7. Review
  8. Mechanism of Rhinovirus Immunity and Asthma.Frontiers in immunology · 2021
    Review
  9. Article
  10. LILRB4, from the immune system to the disease target.American journal of translational research · 2020
    Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Glycyrrhizin AttenuatesFrontiers in immunology · 2018
    Article
  17. 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

6 authors at 2 institutions in 1 country.

Nicholas J CollettiSanofi Pharmaceuticals, Cambridge, MA, USA; Department of Biological Science, Seton Hall University, South Orange, NJ, USA.
Hong LiuSanofi Pharmaceuticals , Cambridge, MA , USA.
Adam C GowerClinical and Translational Science Institute, Boston University , Boston, MA , USA.
Yuriy O AlekseyevDepartment of Pathology and Laboratory Medicine, Boston University , Boston, MA , USA.
Christopher W ArendtSanofi Pharmaceuticals , Cambridge, MA , USA.
Michael H ShawSanofi Pharmaceuticals , Cambridge, MA , USA.
Sanofi (United States) · USBoston University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conventional and plasmacytoid dendritic cells (cDCs and pDCs) are the two populations of DCs that can be readily identified in human blood. Conventional DCs have been subdivided into CD1c(+), or blood dendritic cells antigen (BDCA) 1 and CD141(+), or BDCA-3, DCs, each having both unique gene expression profiles and functions. BDCA-3 DCs express high levels of toll-like receptor 3 and upon stimulation with Poly I:C secrete IFN-β, CXCL10, and IL-12p70. In this article, we show that activation of human BDCA-3 DCs with Poly I:C induces the expression of activation markers (CD40, CD80, and CD86) and immunoglobulin-like transcript (ILT) 3 and 4. This Poly I:C stimulation results in four populations identifiable by flow cytometry based on their expression of ILT3 and ILT4. We focused our efforts on profiling the ILT4(-) and ILT4(+) DCs. These ILT-expressing BDCA-3 populations exhibit similar levels of activation as measured by CD40, CD80, and CD86; however, they exhibit differential cytokine secretion profiles, unique gene signatures, and vary in their ability to prime allogenic naïve T cells. Taken together, these data illustrate that within a pool of BDCA-3 DCs, there are cells poised to respond differently to a given input stimulus with unique output of immune functions.

Indexed as

BDCA-3dendritic cellILT3ILT4TLR3

Identifiers

PMID27014268
PMCPMC4789364
OpenAlexW2305694786

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.