Evaluation of a new bead-based assay to measure levels of human tissue factor antigen in extracellular vesicles in plasma.

COVID‐19 biomarker extracellular vesicle thrombosis tissue factor

Journal

Research and practice in thrombosis and haemostasis
ISSN: 2475-0379
Titre abrégé: Res Pract Thromb Haemost
Pays: United States
ID NLM: 101703775

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 12 01 2022
revised: 03 02 2022
accepted: 08 02 2022
entrez: 14 3 2022
pubmed: 15 3 2022
medline: 15 3 2022
Statut: epublish

Résumé

Circulating tissue factor (TF)-expressing extracellular vesicles (EVs) are associated with thrombosis in several diseases, such as coronavirus disease 2019 (COVID-19). Activity assays have higher sensitivity and specificity compared to antigen assays for measuring TF+ EVs in plasma. The MACSPlex Exosome Kit is designed to detect 37 exosomal surface epitopes, including TF, on EVs in plasma using various fluorescently labeled beads. The different EV-bead complexes are detected by flow cytometry. A recent study used the MACSPlex Exosome Kit to measure levels of TF+ EVs in serum from patients with COVID-19. To evaluate the ability of the MACSPlex Exosome Kit to detect TF on EVs in plasma. We measured levels of TF+ EVs isolated from plasma with or without TF detected using our in-house EVTF activity assay and the MACSPlex Exosome Kit. The MACSPlex Exosome Kit gave a very low TF antigen signal (TF bead signal) compared to platelet-derived CD41b+ EVs, which was used as a control. Lipopolysaccharide (LPS) increased levels of EVTF activity but not TF bead signal in four donors. Inhibition of TF reduced levels of EVTF activity but did not affect the TF bead signal in EVs isolated from plasma from LPS-treated blood. Finally, we found no correlation between levels of EVTF activity and TF bead signal in EVs isolated from plasma from ovarian cancer patients ( Our data suggest that the MACSPlex Exosome Kit gives a nonspecific signal for TF and does not have the sensitivity to detect TF+ EVs in plasma.

Sections du résumé

Background UNASSIGNED
Circulating tissue factor (TF)-expressing extracellular vesicles (EVs) are associated with thrombosis in several diseases, such as coronavirus disease 2019 (COVID-19). Activity assays have higher sensitivity and specificity compared to antigen assays for measuring TF+ EVs in plasma. The MACSPlex Exosome Kit is designed to detect 37 exosomal surface epitopes, including TF, on EVs in plasma using various fluorescently labeled beads. The different EV-bead complexes are detected by flow cytometry. A recent study used the MACSPlex Exosome Kit to measure levels of TF+ EVs in serum from patients with COVID-19.
Objectives UNASSIGNED
To evaluate the ability of the MACSPlex Exosome Kit to detect TF on EVs in plasma.
Methods UNASSIGNED
We measured levels of TF+ EVs isolated from plasma with or without TF detected using our in-house EVTF activity assay and the MACSPlex Exosome Kit.
Results UNASSIGNED
The MACSPlex Exosome Kit gave a very low TF antigen signal (TF bead signal) compared to platelet-derived CD41b+ EVs, which was used as a control. Lipopolysaccharide (LPS) increased levels of EVTF activity but not TF bead signal in four donors. Inhibition of TF reduced levels of EVTF activity but did not affect the TF bead signal in EVs isolated from plasma from LPS-treated blood. Finally, we found no correlation between levels of EVTF activity and TF bead signal in EVs isolated from plasma from ovarian cancer patients (
Conclusion UNASSIGNED
Our data suggest that the MACSPlex Exosome Kit gives a nonspecific signal for TF and does not have the sensitivity to detect TF+ EVs in plasma.

Identifiants

pubmed: 35284777
doi: 10.1002/rth2.12677
pii: S2475-0379(22)01168-2
pmc: PMC8897283
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e12677

Subventions

Organisme : NHLBI NIH HHS
ID : R35 HL155657
Pays : United States

Informations de copyright

© 2022 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis (ISTH).

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Auteurs

Sierra J Archibald (SJ)

Division of Hematology UNC Blood Research Center University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.

Yohei Hisada (Y)

Division of Hematology UNC Blood Research Center University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.

Victoria L Bae-Jump (VL)

Division of Gynecologic Oncology University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.
Lineberger Comprehensive Cancer Center Department of Medicine University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.

Nigel Mackman (N)

Division of Hematology UNC Blood Research Center University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.

Classifications MeSH