Evidence map›Paper›PMID 31548524›Full record

ArticleAntibodies (Basel, Switzerland)2017

Potential Roles of Antiphospholipid Antibodies in Generating Platelet-C4d in Systemic Lupus Erythematosus.

Chau-Ching Liu, Travis Schofield, Amy Tang, Susan Manzi, Joseph M Ahearn

Open access · goldAbstract read
In one paragraph

Article in Antibodies (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 89% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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.

Chau-Ching LiuLupus Center of Excellence, Autoimmunity Institute, Allegheny Health Network Research Institute, Allegheny Health Network, Pittsburgh 15212, PA, USA. chauching.liu@ahn.org.
Travis SchofieldLupus Center of Excellence, Autoimmunity Institute, Allegheny Health Network Research Institute, Allegheny Health Network, Pittsburgh 15212, PA, USA. txs101TSS@aol.com.
Amy TangLupus Center of Excellence, Autoimmunity Institute, Allegheny Health Network Research Institute, Allegheny Health Network, Pittsburgh 15212, PA, USA. amy.tang@ahn.org.
Susan ManziLupus Center of Excellence, Autoimmunity Institute, Allegheny Health Network Research Institute, Allegheny Health Network, Pittsburgh 15212, PA, USA. susan.manzi@ahn.org.
Joseph M AhearnLupus Center of Excellence, Autoimmunity Institute, Allegheny Health Network Research Institute, Allegheny Health Network, Pittsburgh 15212, PA, USA. joseph.ahearn@ahn.org.
Allegheny Health Network · US

Funding

Department of Defense Peer Reviewed Medical Research Grant W81XWH-06-2-0038
6 · The paper itself

Abstract

Premature, accelerated onset of atherothrombotic disease is prevalent in patients with systemic lupus erythematosus (SLE). Most, if not all, atherothrombotic diseases are likely to involve platelets and complement. Previously, we discovered that platelets bearing complement activation product C4d (P-C4d) are present in SLE patients, and are significantly associated with antiphospholipid (aPL) antibody positivity and stroke in SLE patients. The goal of the present study was to further elucidate the role of aPL and other platelet-reactive autoantibodies in the generation of P-C4d. To determine the association between P-C4d and aPL antibodies, the serum levels of aPL antibodies and P-C4d of 180 SLE patients were measured by enzyme-linked immunoassays and flow cytometry, respectively. To investigate the role of aPL antibodies, and possibly other autoantibodies as well, in mediating the generation of P-C4d, in vitro 2-step P-C4d induction experiments were performed. The results showed that the presence and levels of aPL antibodies in the serum were specifically elevated in SLE patients with positive P-C4d. The plasma and immunoglobulins purified from SLE patients who were positive for P-C4d and aPL were capable of inducing C4d deposition on normal platelets in vitro. The capacity of SLE plasma in inducing P-C4d appeared to correlate proportionately to the serum aPL levels. Collectively, the results demonstrate that both aPL and other platelet-reactive autoantibodies may participate in mediating the generation of P-C4d in SLE patients.

Indexed as

anti-cardiolipin antibodiesantiphospholipid antibodiesanti-β2 glycoprotein I antibodiescell-bound complement activation products (CB-CAPs)complementplateletsystemic lupus erythematosus

Identifiers

PMID31548524
PMCPMC6698828
OpenAlexW2733821833

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.