Antiphospholipid antibodies in patients with stroke during COVID-19: A role in the signaling pathway leading to platelet activation

BackgroundSeveral viral and bacterial infections, including COVID-19, may lead to both thrombotic and hemorrhagic complications. Previously, it has been demonstrated an “in vitro” pathogenic effect of “antiphospholipid” antibodies (aPLs), which are able to activate a proinflammatory and procoagulant...

Full description

Bibliographic Details
Main Authors: Antonella Capozzi, Gloria Riitano, Serena Recalchi, Valeria Manganelli, Agostina Longo, Anne Falcou, Manuela De Michele, Tina Garofalo, Fabio M. Pulcinelli, Maurizio Sorice, Roberta Misasi
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-03-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2023.1129201/full
_version_ 1811161764366123008
author Antonella Capozzi
Gloria Riitano
Serena Recalchi
Valeria Manganelli
Agostina Longo
Anne Falcou
Manuela De Michele
Tina Garofalo
Fabio M. Pulcinelli
Maurizio Sorice
Roberta Misasi
author_facet Antonella Capozzi
Gloria Riitano
Serena Recalchi
Valeria Manganelli
Agostina Longo
Anne Falcou
Manuela De Michele
Tina Garofalo
Fabio M. Pulcinelli
Maurizio Sorice
Roberta Misasi
author_sort Antonella Capozzi
collection DOAJ
description BackgroundSeveral viral and bacterial infections, including COVID-19, may lead to both thrombotic and hemorrhagic complications. Previously, it has been demonstrated an “in vitro” pathogenic effect of “antiphospholipid” antibodies (aPLs), which are able to activate a proinflammatory and procoagulant phenotype in monocytes, endothelial cells and platelets. This study analyzed the occurrence of aPL IgG in patients with acute ischemic stroke (AIS) during COVID-19, evaluating the effect of Ig fractions from these patients on signaling and functional activation of platelets.Materials and methodsSera from 10 patients with AIS during COVID-19, 10 non-COVID-19 stroke patients, 20 COVID-19 and 30 healthy donors (HD) were analyzed for anti-cardiolipin, anti-β2-GPI, anti-phosphatidylserine/prothrombin and anti-vimentin/CL antibodies by ELISA. Platelets from healthy donors were incubated with Ig fractions from these patients or with polyclonal anti-β2-GPI IgG and analyzed for phospho-ERK and phospho-p38 by western blot. Platelet secretion by ATP release dosage was also evaluated.ResultsWe demonstrated the presence of aPLs IgG in sera of patients with AIS during COVID-19. Treatment with the Ig fractions from these patients or with polyclonal anti-β2-GPI IgG induced a significant increase of phospho-ERK and phospho-p38 expression. In the same vein, platelet activation was supported by the increase of adenyl nucleotides release induced by Ig fractions.ConclusionsThis study demonstrates the presence of aPLs in a subgroup of COVID-19 patients who presented AIS, suggesting a role in the mechanisms contributing to hypercoagulable state in these patients. Detecting these antibodies as a serological marker to check and monitor COVID-19 may contribute to improve the risk stratification of thromboembolic manifestations in these patients.
first_indexed 2024-04-10T06:19:26Z
format Article
id doaj.art-55e066f3b315407ea5cf5b6dd849935f
institution Directory Open Access Journal
issn 1664-3224
language English
last_indexed 2024-04-10T06:19:26Z
publishDate 2023-03-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Immunology
spelling doaj.art-55e066f3b315407ea5cf5b6dd849935f2023-03-02T05:01:41ZengFrontiers Media S.A.Frontiers in Immunology1664-32242023-03-011410.3389/fimmu.2023.11292011129201Antiphospholipid antibodies in patients with stroke during COVID-19: A role in the signaling pathway leading to platelet activationAntonella Capozzi0Gloria Riitano1Serena Recalchi2Valeria Manganelli3Agostina Longo4Anne Falcou5Manuela De Michele6Tina Garofalo7Fabio M. Pulcinelli8Maurizio Sorice9Roberta Misasi10Department of Experimental Medicine, “Sapienza” University of Rome, Rome, ItalyDepartment of Experimental Medicine, “Sapienza” University of Rome, Rome, ItalyDepartment of Experimental Medicine, “Sapienza” University of Rome, Rome, ItalyDepartment of Experimental Medicine, “Sapienza” University of Rome, Rome, ItalyDepartment of Experimental Medicine, “Sapienza” University of Rome, Rome, ItalyEmergency Department, “Sapienza” University of Rome, Rome, ItalyEmergency Department, “Sapienza” University of Rome, Rome, ItalyDepartment of Experimental Medicine, “Sapienza” University of Rome, Rome, ItalyDepartment of Experimental Medicine, “Sapienza” University of Rome, Rome, ItalyDepartment of Experimental Medicine, “Sapienza” University of Rome, Rome, ItalyDepartment of Experimental Medicine, “Sapienza” University of Rome, Rome, ItalyBackgroundSeveral viral and bacterial infections, including COVID-19, may lead to both thrombotic and hemorrhagic complications. Previously, it has been demonstrated an “in vitro” pathogenic effect of “antiphospholipid” antibodies (aPLs), which are able to activate a proinflammatory and procoagulant phenotype in monocytes, endothelial cells and platelets. This study analyzed the occurrence of aPL IgG in patients with acute ischemic stroke (AIS) during COVID-19, evaluating the effect of Ig fractions from these patients on signaling and functional activation of platelets.Materials and methodsSera from 10 patients with AIS during COVID-19, 10 non-COVID-19 stroke patients, 20 COVID-19 and 30 healthy donors (HD) were analyzed for anti-cardiolipin, anti-β2-GPI, anti-phosphatidylserine/prothrombin and anti-vimentin/CL antibodies by ELISA. Platelets from healthy donors were incubated with Ig fractions from these patients or with polyclonal anti-β2-GPI IgG and analyzed for phospho-ERK and phospho-p38 by western blot. Platelet secretion by ATP release dosage was also evaluated.ResultsWe demonstrated the presence of aPLs IgG in sera of patients with AIS during COVID-19. Treatment with the Ig fractions from these patients or with polyclonal anti-β2-GPI IgG induced a significant increase of phospho-ERK and phospho-p38 expression. In the same vein, platelet activation was supported by the increase of adenyl nucleotides release induced by Ig fractions.ConclusionsThis study demonstrates the presence of aPLs in a subgroup of COVID-19 patients who presented AIS, suggesting a role in the mechanisms contributing to hypercoagulable state in these patients. Detecting these antibodies as a serological marker to check and monitor COVID-19 may contribute to improve the risk stratification of thromboembolic manifestations in these patients.https://www.frontiersin.org/articles/10.3389/fimmu.2023.1129201/fullantiphospholipid antibodiesβ2-GPICOVID-19thrombosisstroke.
spellingShingle Antonella Capozzi
Gloria Riitano
Serena Recalchi
Valeria Manganelli
Agostina Longo
Anne Falcou
Manuela De Michele
Tina Garofalo
Fabio M. Pulcinelli
Maurizio Sorice
Roberta Misasi
Antiphospholipid antibodies in patients with stroke during COVID-19: A role in the signaling pathway leading to platelet activation
Frontiers in Immunology
antiphospholipid antibodies
β2-GPI
COVID-19
thrombosis
stroke.
title Antiphospholipid antibodies in patients with stroke during COVID-19: A role in the signaling pathway leading to platelet activation
title_full Antiphospholipid antibodies in patients with stroke during COVID-19: A role in the signaling pathway leading to platelet activation
title_fullStr Antiphospholipid antibodies in patients with stroke during COVID-19: A role in the signaling pathway leading to platelet activation
title_full_unstemmed Antiphospholipid antibodies in patients with stroke during COVID-19: A role in the signaling pathway leading to platelet activation
title_short Antiphospholipid antibodies in patients with stroke during COVID-19: A role in the signaling pathway leading to platelet activation
title_sort antiphospholipid antibodies in patients with stroke during covid 19 a role in the signaling pathway leading to platelet activation
topic antiphospholipid antibodies
β2-GPI
COVID-19
thrombosis
stroke.
url https://www.frontiersin.org/articles/10.3389/fimmu.2023.1129201/full
work_keys_str_mv AT antonellacapozzi antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation
AT gloriariitano antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation
AT serenarecalchi antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation
AT valeriamanganelli antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation
AT agostinalongo antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation
AT annefalcou antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation
AT manuelademichele antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation
AT tinagarofalo antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation
AT fabiompulcinelli antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation
AT mauriziosorice antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation
AT robertamisasi antiphospholipidantibodiesinpatientswithstrokeduringcovid19aroleinthesignalingpathwayleadingtoplateletactivation