Evidence map›Paper›PMID 30712125›Full record

ReviewCurrent rheumatology reports2019

SLE-associated risk factors affect DC function.

Sun Jung Kim

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current rheumatology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

1 author.

Sun Jung KimCenter for Autoimmune and Musculoskeletal Disease, Department of Molecular Medicine, The Feinstein Institute for Medical Research, School of Medicine at Northwell-Hofstra University, 350 Community Drive, Manhasset, NY, 11030, USA. SJKIM@NORTHWELL.EDU.

Funding

The Blimp-1 SLE risk variant regulates inflammatory function in dendritic cellsR01AR065209 · NIAMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI KIM, SUN JUNG · 2014 to 2017
$1.8M
Function of Blimp1/prdm-1 in dendritic cells in the generation of autoantibodiesK01AR059378 · NIAMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI KIM, SUN JUNG · 2010 to 2014
$568k
NIAMS NIH HHS K01 AR059378NIAMS NIH HHS R01 AR065209
6 · The paper itself

Abstract

purpose of reviewIdentification of function and potential pathogenic mechanisms of SLE risk genes in dendritic cells. RECENT

findingsFunctional studies of individual SLE risk factors in dendritic cells were performed, and functional alterations of some risk genes in dendritic cells were observed. Recent studies confirmed the pathogenic function of known risk genes. These findings postulate novel pathogenic mechanisms made by dendritic cells. SLE is a complex disease and its etiology is not clearly understood. Dendritic cells are innate immune cells and critical for determining immune activation and immune tolerance. Genetic studies identified several new candidate genes which predispose to development of autoimmune diseases, but the mechanism of those genes has not been identified. This report updates functional implications or pathways in dendritic cells which are putatively important for the development or propagation of SLE based on genetic and functional studies performed in both human and animal models.

Indexed as

AnimalsAntigen PresentationDendritic CellsGenetic Predisposition to DiseaseHumansImmune ToleranceLupus Erythematosus, SystemicPolymorphism, Single NucleotideReceptors, IgGRisk FactorsReceptors, IgGDendritic cellsgenetic risk factorsSLE

Identifiers

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.