Evidence map›Paper›PMID 33182499›Full record

ReviewInternational journal of molecular sciences2020

Molecular Mechanisms of "Antiphospholipid Antibodies" and Their Paradoxical Role in the Pathogenesis of "Seronegative APS".

Roberta Misasi, Agostina Longo, Serena Recalchi, Daniela Caissutti, Gloria Riitano, Valeria Manganelli, Tina Garofalo, Maurizio Sorice, Antonella Capozzi

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Effect of vitamin DClinics (Sao Paulo, Brazil) · 2024
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  17. Autoantibodies: are they a clue for liver diseases?Clinical and experimental hepatology · 2022
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  19. Article
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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

9 authors at 1 institution in 1 country.

Roberta MisasiDepartment of Experimental Medicine, University of Rome "La Sapienza", 00161 Rome, Italy.
Agostina LongoDepartment of Experimental Medicine, University of Rome "La Sapienza", 00161 Rome, Italy.
Serena RecalchiDepartment of Experimental Medicine, University of Rome "La Sapienza", 00161 Rome, Italy.
Daniela CaissuttiDepartment of Experimental Medicine, University of Rome "La Sapienza", 00161 Rome, Italy.
Gloria RiitanoDepartment of Experimental Medicine, University of Rome "La Sapienza", 00161 Rome, Italy.
Valeria ManganelliDepartment of Experimental Medicine, University of Rome "La Sapienza", 00161 Rome, Italy.
Tina GarofaloDepartment of Experimental Medicine, University of Rome "La Sapienza", 00161 Rome, Italy.
Maurizio SoriceDepartment of Experimental Medicine, University of Rome "La Sapienza", 00161 Rome, Italy.
Antonella CapozziDepartment of Experimental Medicine, University of Rome "La Sapienza", 00161 Rome, Italy.
Sapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antiphospholipid Syndrome (APS) is an autoimmune disease characterized by arterial and/or venous thrombosis and/or pregnancy morbidity, associated with circulating antiphospholipid antibodies (aPL). In some cases, patients with a clinical profile indicative of APS (thrombosis, recurrent miscarriages or fetal loss), who are persistently negative for conventional laboratory diagnostic criteria, are classified as "seronegative" APS patients (SN-APS). Several findings suggest that aPL, which target phospholipids and/or phospholipid binding proteins, mainly β-glycoprotein I (β-GPI), may contribute to thrombotic diathesis by interfering with hemostasis. Despite the strong association between aPL and thrombosis, the exact pathogenic mechanisms underlying thrombotic events and pregnancy morbidity in APS have not yet been fully elucidated and multiple mechanisms may be involved. Furthermore, in many SN-APS patients, it is possible to demonstrate the presence of unconventional aPL ("non-criteria" aPL) or to detect aPL with alternative laboratory methods. These findings allowed the scientists to study the pathogenic mechanism of SN-APS. This review is focused on the evidence showing that these antibodies may play a functional role in the signal transduction pathway(s) leading to thrombosis and pregnancy morbidity in SN-APS. A better comprehension of the molecular mechanisms triggered by aPL may drive development of potential therapeutic strategies in APS patients.

Indexed as

AnimalsAntibodies, AntiphospholipidAntiphospholipid SyndromeAutoimmune DiseasesFemaleHumansPregnancySignal TransductionThrombosisAntibodies, Antiphospholipidlipid rafts“non-criteria” aPLPTMsSN-APSTLR-4 pathwaysβ2GPI

Identifiers

PMID33182499
PMCPMC7665122
OpenAlexW3106120788

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.