Evidence map›Paper›PMID 27257889›Full record

ArticlePloS one2016

Novel Phospholipid-Protein Conjugates Allow Improved Detection of Antibodies in Patients with Autoimmune Diseases.

Simone V Samuelsen, Arindam Maity, Mads Nybo, Claudia Macaubas, Lars Lønstrup, Imelda M Balboni, Elizabeth D Mellins, Kira Astakhova

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. 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
0.3field-weighted citation impact, top 36% 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

8 authors at 3 institutions in 2 countries.

Simone V SamuelsenDepartment of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense, Denmark.
Arindam MaityDepartment of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense, Denmark.
Mads NyboDepartment of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense, Denmark.
Claudia MacaubasDepartment of Pediatrics, Program in Immunology, Stanford University, Stanford, California, United States of America.
Lars LønstrupDepartment of Business and Economics, University of Southern Denmark, Odense, Denmark.
Imelda M BalboniDepartment of Pediatrics, Program in Immunology, Stanford University, Stanford, California, United States of America.
Elizabeth D MellinsDepartment of Pediatrics, Program in Immunology, Stanford University, Stanford, California, United States of America.
Kira AstakhovaDepartment of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense, Denmark.
University of Southern Denmark · DKStanford University · USOdense University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reliable measurement of clinically relevant autoimmune antibodies toward phospholipid-protein conjugates is highly desirable in research and clinical assays. To date, the development in this field has been limited to the use of natural heterogeneous antigens. However, this approach does not take structural features of biologically active antigens into account and leads to low reliability and poor scientific test value. Here we describe novel phospholipid-protein conjugates for specific detection of human autoimmune antibodies. Our synthetic approach includes mild oxidation of synthetic phospholipid cardiolipin, and as the last step, coupling of the product with azide-containing linker and copper-catalyzed click chemistry with β2-glycoprotein I and prothrombin. To prove utility of the product antigens, we used enzyme-linked immunosorbent assay and three cohorts of samples obtained from patients in Denmark (n = 34) and the USA (n = 27 and n = 14). Afterwards we analyzed correlation of the obtained autoantibody titers with clinical parameters for each patient. Our results prove that using novel antigens clinically relevant autoantibodies can be detected with high repeatability, sensitivity and specificity. Unlike previously used antigens the obtained autoantibody titers strongly correlate with high disease activity and in particular, with arthritis, renal involvement, anti-Smith antibodies and high lymphocyte count. Importantly, chemical composition of antigens has a strong influence on the correlation of detected autoantibodies with disease activity and manifestations. This confirms the crucial importance of antigens' composition on research and diagnostic assays, and opens up exciting perspectives for synthetic antigens in future studies of autoimmunity.

Indexed as

AdolescentAntibodies, AntiphospholipidAutoantibodiesAutoimmune DiseasesChildFemaleHumansMaleReproducibility of ResultsYoung AdultAntibodies, AntiphospholipidAutoantibodies

Identifiers

PMID27257889
PMCPMC4892602
OpenAlexW2413537431

What OpenQuestion holds

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LicenceCC BY
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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.