Evidence map›Paper›PMID 23131610›Full record

ReviewCurrent opinion in immunology2012

The pathogenesis of systemic lupus erythematosus-an update.

Jinyoung Choi, Sang Taek Kim, Joe Craft

Registry-linked trialAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03189017 (A Phase I Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Trial in Healthy Subjects to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ICP-022 Following Single and Multiple Escalating Dose), which is not on this map. Cited by 147 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
147citing papers in PubMed, 7 pooled it
–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.

NCT03189017 phase1completednot on this mapstarted 2017, after this paper: background citation

A Phase I Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Trial in Healthy Subjects to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ICP-022 Following Single and Multiple Escalating Dose

TypeinterventionalSponsorInnocare Pharma Australia Pty LtdRan2017 to 2018Enrolled64ConditionsSystemic Lupus Erythematosus, Rheumatoid ArthritisArmsICP-022, Placebos
3 · Its place in the literature

Who cites it

147 citing papers in PubMed, 7 syntheses or guidelines pooled it.

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  13. Biological multi-omics approaches to next-generation biomarkers in immune-related disorders and malignancies: An overview.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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87 more citing papers are in PubMed but not listed here.

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

3 authors.

Jinyoung ChoiDepartment of Internal Medicine (Rheumatology), Yale School of Medicine, New Haven, CT 06520, United States.
Sang Taek Kim
Joe Craft

Funding

TRAINING PROGRAM IN INVESTIGATIVE RHEUMATOLOGYT32AR007107 · NIAMS · YALE UNIVERSITY · PI RICHARD J BUCALA · 1986 to 2026
$7.5M
IMMUNE RESPONSES IN LUPUSR37AR040072 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2000 to 2025
$7.4M
Yale Rheumatic Diseases Research Core CenterP30AR053495 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2007 to 2017
$7.0M
GENETIC ANALYSIS OF T CELLS IN LUPUSR01AR044076 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 1996 to 2010
$4.1M
MOLECULAR CHARACTERIZATION OF THE SNRNP POLYPEPTIDESR01AR040072 · NIAMS · YALE UNIVERSITY · PI Joseph Edgar Craft · 1990 to 2026
$2.5M
Dissecting the role for IL-15 in CD8+ T cell homeostasis in human lupusR01AI075157 · NIAID · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2008 to 2012
$2.0M
Manipulation of Follicular Helper T Cells in Immunity and AutoimmunityR21AR063942 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2012 to 2013
$402k
A Novel B Cell Marker and Therapeutic Target in LupusR21AR062842 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2012 to 2013
$402k
NIAID NIH HHS AI075157NIAID NIH HHS R01 AI075157NIAMS NIH HHS AR053495NIAMS NIH HHS AR40072NIAMS NIH HHS AR44076NIAMS NIH HHS P30 AR053495NIAMS NIH HHS R01 AR040072NIAMS NIH HHS R01 AR044076NIAMS NIH HHS R21 AR062842NIAMS NIH HHS R21 AR063942NIAMS NIH HHS R37 AR040072NIAMS NIH HHS T32 AR007107
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE, lupus) is characterized by a global loss of self-tolerance with activation of autoreactive T and B cells leading to production of pathogenic autoantibodies and tissue injury. Innate immune mechanisms are necessary for the aberrant adaptive immune responses in SLE. Recent advances in basic and clinical biology have shed new light on disease mechanisms in lupus, with this review discussing the recent studies that offer valuable insights into disease-specific therapeutic targets.

Indexed as

AutoantibodiesAutoimmunityB-LymphocytesHumansImmunity, InnateLupus Erythematosus, SystemicT-LymphocytesAutoantibodies

Identifiers

PMID23131610
PMCPMC3508331

What OpenQuestion holds

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Registered trials

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.