Evidence map›Paper›PMID 21945394›Full record

ArticleJournal of immunological methods2012

A quantitative proteomic approach for detecting protein profiles of activated human myeloid dendritic cells.

Daniela M Schlatzer, Julia Sugalski, Jean-Eudes Dazard, Mark R Chance, Donald D Anthony

Abstract read
In one paragraph

Article in Journal of immunological methods, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings.American journal of medical genetics. Part A · 2017
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

5 authors at 1 institution in 1 country.

Daniela M SchlatzerCenter for Proteomics and Bioinformatics, Case Western Reserve University, Cleveland, OH 44106, United States. dms73@case.edu
Julia Sugalski
Jean-Eudes Dazard
Mark R Chance
Donald D Anthony
Case Western Reserve University · US

Funding

WG3: HIV, Co-infections and Co-morbiditiesP30AI036219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI Sharon L. Hillier, JONATHAN KARN · 1994 to 2026
$50.0M
Proteomics of Immune Restoration and Opioid Exposure in HIV DiseaseP20DA026133 · NIDA · CASE WESTERN RESERVE UNIVERSITY · PI ANTHONY, DONALD D · 2009 to 2011
$3.0M
Role of immature DC in host defense against HCVR01DK068361 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI ANTHONY, DONALD D · 2006 to 2010
$1.3M
NIAID NIH HHS AI 36219NIAID NIH HHS P30 AI036219NIDA NIH HHS P20 DA026133NIDA NIH HHS P20-DA-026133NIDDK NIH HHS R01 DK068361
6 · The paper itself

Abstract

Dendritic cells (DC) direct the magnitude, polarity and effector function of the adaptive immune response. DC express toll-like receptors (TLR), antigen capturing and processing machinery, and costimulatory molecules, which facilitate innate sensing and T cell activation. Once activated, DC can efficiently migrate to lymphoid tissue and prime T cell responses. Therefore, DC play an integral role as mediators of the immune response to multiple pathogens. Elucidating the molecular mechanisms involved in DC activation is therefore central in gaining an understanding of host response to infection. Unfortunately, technical constraints have limited system-wide 'omic' analysis of human DC subsets collected ex vivo. Here we have applied novel proteomic approaches to human myeloid dendritic cells (mDCs) purified from 100 mL of peripheral blood to characterize specific molecular networks of cell activation at the individual patient level, and have successfully quantified over 700 proteins from individual samples containing as little as 200,000 mDCs. The proteomic and network readouts after ex vivo stimulation of mDCs with TLR3 agonists are measured and verified using flow cytometry.

Indexed as

AdultDendritic CellsFemaleFlow CytometryHumansLymphocyte ActivationMaleMiddle AgedMyeloid CellsProteomicsReproducibility of ResultsSensitivity and SpecificityT-LymphocytesToll-Like Receptor 3TLR3 protein, humanToll-Like Receptor 3

Identifiers

PMID21945394
PMCPMC3253886
OpenAlexW2050744869

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.