Evidence map›Paper›PMID 26683146›Full record

ReviewImmunological reviews2016

Endosomal Toll-like receptors in clinically overt and silent autoimmunity.

Robert M Clancy, Androo J Markham, Jill P Buyon

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

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  10. Mobilization of innate and adaptive antitumor immune responses by the RNP-targeting antibody ATRC-101.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Biomarkers in the Light of the Etiopathology of IC/BPS.Diagnostics (Basel, Switzerland) · 2021
    Review
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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 at 1 institution in 1 country.

Robert M ClancyDivision of Rheumatology, Department of Medicine, New York University School of Medicine, New York, NY, USA.
Androo J MarkhamDivision of Rheumatology, Department of Medicine, New York University School of Medicine, New York, NY, USA.
Jill P BuyonDivision of Rheumatology, Department of Medicine, New York University School of Medicine, New York, NY, USA.
New York University · US

Funding

Maternal Autoantibodies: Pathogenesis of Neonatal LupusR37AR042455 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BUYON, JILL P · 2008 to 2018
$4.0M
Preventive Approach to Congenital Heart Block with Hydroxychloroquine (PATCH)R01HD079951 · NICHD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BUYON, JILL P · 2015 to 2019
$1.4M
Preventive Approach to Congenital Heart Block with Hydroxychloroquine (PATCH)R03HD069986 · NICHD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BUYON, JILL P · 2012 to 2014
$249k
RESEARCH REGISTRY FOR NEONATAL LUPUS-264942220N01AR042220 · NIAMS · HOSPITAL FOR JOINT DISEASES ORTHO INST · 1994 to 2003
$148k
NIAMS NIH HHS 3R37AR042455-21S1NIAMS NIH HHS 3R37AR042455-21S2NIAMS NIH HHS N01 AR042220NIAMS NIH HHS N01-AR-4-2220NIAMS NIH HHS R37 AR042455NIAMS NIH HHS R37AR042455NICHD NIH HHS 1 R01 HD079951-01A1NICHD NIH HHS R01 HD079951NICHD NIH HHS R03 HD069986
6 · The paper itself

Abstract

Toll-like receptors (TLRs), first identified as pattern recognition receptors, are now recognized to serve as a key interface between innate and adaptive immunity. Systemic lupus erythematosus (SLE) is characterized by both continuous and cyclic stimulation of the innate and adaptive immune system by endogenous nucleic acids released from apoptotic or necrotic cells. TLR7 and TLR9 function as innate sensors of viral infection as their ligands are ssRNA and dsDNA, respectively. Recognition of self nucleic acids by endosomal TLRs in B cells and pDCs is thought to be an important step in the pathogenesis of SLE, generating anti-nuclear antibodies and producing type I IFN. In this review, we take a specific look at how TLR7, non-coding RNA, and SSA/Ro60 can contribute to clinical autoimmunity and organ damage in the context of neonatal lupus (NL). Although 15 times less common than SLE, NL provides a unique opportunity to study two different aspects of autoimmunity: passively acquired tissue injury in a developing fetus and clinical progression of disease in an asymptomatic mother found to have anti-Ro60 autoantibodies only after identification of heart block/rash in a child. Finally, we discuss hydroxychloroquine (HCQ) use by asymptomatic subjects which may forestall the clinical expression of autoimmunity.

Indexed as

AnimalsAsymptomatic DiseasesAutoantibodiesAutoimmunityEndosomesHeart BlockHumansHydroxychloroquineImmunity, Maternally-AcquiredInfant, NewbornLupus Erythematosus, SystemicRibonucleoproteinsSS-A AntigenToll-Like Receptor 7AutoantibodiesHydroxychloroquineRibonucleoproteinsSS-A AntigenToll-Like Receptor 7anti-SSA/Ro60autoimmunitylupusneonatal lupusTLR7

Identifiers

PMID26683146
PMCPMC4685960
OpenAlexW2209284337

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.