Evidence map›Paper›PMID 24829416›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Targeting antigens through blood dendritic cell antigen 2 on plasmacytoid dendritic cells promotes immunologic tolerance.

Craig P Chappell, Natalia V Giltiay, Kevin E Draves, ChangHung Chen, Martha S Hayden-Ledbetter, Mark J Shlomchik, Daniel H Kaplan, Edward A Clark

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. 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
1.7field-weighted citation impact, top 16% 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, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. FOXP3-Positive Regulatory T Cells and Kidney Allograft Tolerance.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2017
    Review
  10. Article
  11. Review
  12. Article
  13. Human dendritic cell subsets and function in health and disease.Cellular and molecular life sciences : CMLS · 2015
    Review
  14. Review
  15. Review
  16. Review
  17. 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

8 authors at 4 institutions in 1 country.

Craig P Chappell *Department of Immunology, School of Medicine, University of Washington, Seattle, WA, USA.
Natalia V Giltiay *Department of Immunology, School of Medicine, University of Washington, Seattle, WA, USA.
Kevin E DravesDepartment of Immunology, School of Medicine, University of Washington, Seattle, WA, USA.
ChangHung ChenElAb Bio, Gaithersburg MD.
Martha S Hayden-LedbetterDepartment of Immunology, School of Medicine, University of Washington, Seattle, WA, USA.
Mark J ShlomchikDepartment of Immunology, School of Medicine, University of Pittsburg, Pittsburg, PA, USA.
Daniel H KaplanDepartment of Dermatology, University of Minnesota Medical School, Minneapolis, MN, USA.
Edward A ClarkDepartment of Immunology, School of Medicine, University of Washington, Seattle, WA, USA.
University of Washington · USQuality Biological · USUniversity of Minnesota Medical Center · USUniversity of Pittsburgh · US

Funding

Programming protective immunity by targeting antigens to the CD180 receptorR01AI052203 · NIAID · UNIVERSITY OF WASHINGTON · PI FULLER, DEBORAH H. · 2003 to 2019
$6.3M
FDRC1 AND FOLLICULAR DENDRITIC CELL SIGNALING PATHWAYSR37AI044257 · NIAID · UNIVERSITY OF WASHINGTON · PI CLARK, EDWARD A · 2004 to 2013
$4.0M
Role of B cell activating factor (BAFF) in B cell responses and autoimmunityR01AI044257 · NIAID · UNIVERSITY OF WASHINGTON · PI GILTIAY, NATALIA V · 1999 to 2020
$3.7M
NIAID NIH HHS AI44257NIAID NIH HHS AI52203NIAID NIH HHS R01 AI044257NIAID NIH HHS R01 AI052203NIAID NIH HHS R37 AI044257
6 · The paper itself

Abstract

The C-type lectin receptor blood dendritic cell Ag 2 (BDCA2) is expressed exclusively on human plasmacytoid DCs (pDCs) and plays a role in Ag capture, internalization, and presentation to T cells. We used transgenic mice that express human BDCA2 and anti-BDCA2 mAbs to deliver Ags directly to BDCA2 on pDCs in vivo. Targeting Ag to pDCs in this manner resulted in significant suppression of Ag-specific CD4(+) T cell and Ab responses upon secondary exposure to Ag in the presence of adjuvant. Suppression of Ab responses required both a decrease in effector CD4(+) T cells and preservation of Foxp3(+) regulatory T cells (Tregs). Reduction in Treg numbers following Ag delivery to BDCA2 restored both CD4(+) T cell activation and Ab responses, demonstrating that Tregs were required for the observed tolerance. Our results demonstrate that Ag delivery to pDCs through BDCA2 is an effective method to induce immunological tolerance, which may be useful for treating autoimmune diseases or to inhibit unwanted Ab responses.

Indexed as

AnimalsDendritic CellsHumansImmune ToleranceLectins, C-TypeMembrane GlycoproteinsMiceMice, TransgenicPlasma CellsReceptors, ImmunologicT-Lymphocytes, RegulatoryCLEC4C protein, humanLectins, C-TypeMembrane GlycoproteinsReceptors, Immunologic

Identifiers

PMID24829416
PMCPMC4048786
OpenAlexW2129152169

What OpenQuestion holds

Textmetadata
LicenceTDM
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.