Evidence map›Paper›PMID 41282766›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Pathogenic PF4/Polyvinylsulfonate ELISA-negative Antibodies in HIT.

Adam J Kanack, Noah P Splinter, Emily E Mauch, Leben Tefera, Morayma Reyes Gil, Sakshi Jasra, Andrew Goodwin, Kristi J Smock, Hadiyah Ahmad, Aneel Ashrani and 15 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors.

Adam J KanackDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
Noah P SplinterDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
Emily E MauchDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
Leben TeferaDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
Morayma Reyes GilDepartment of Laboratory Medicine, Cleveland Clinic, Cleveland, OH.
Sakshi JasraDepartment of Medicine, University of Vermont, Burlington, VT.
Andrew GoodwinDepartment of Pathology, University of Vermont, Burlington, VT.
Kristi J SmockDepartment of Pathology, Spencer Fox Eccles School of Medicine at the University of Utah, Salt Lake City, UT.
Hadiyah AhmadDepartment of Medicine, Mayo Clinic, Rochester, MN.
Aneel AshraniDepartment of Medicine, Mayo Clinic, Rochester, MN.
Nathaniel L RobinsonDepartment of Surgery, Mayo Clinic, Rochester, MN.
Ana I CasanegraDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.
Curtis G JonesRetham Technologies, Wauwatosa, WI.
Shannon M PechauerVersiti Blood Research Institute, Milwaukee, WI.
Erin YttreVersiti Blood Research Institute, Milwaukee, WI.
Richard H AsterVersiti Blood Research Institute, Milwaukee, WI.
Mindy C KohlhagenDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
Rachel R LegerDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
David L MurrayDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
Lu ZhouVersiti Blood Research Institute, Milwaukee, WI.
Demin WangVersiti Blood Research Institute, Milwaukee, WI.
Renren WenVersiti Blood Research Institute, Milwaukee, WI.
Dong ChenDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
Rajiv K PruthiDepartment of Medicine, Mayo Clinic, Rochester, MN.
Anand PadmanabhanDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.

Funding

The Immunobiology of Vaccine-induced Immune Thrombotic ThrombocytopeniaP01HL167668 · NHLBI · VERSITI WISCONSIN, INC. · PI Peter J Newman · 2024 to 2026
$10.1M
B cell responses in heparin-induced thrombocytopeniaR01HL130724 · NHLBI · VERSITI WISCONSIN, INC. · PI WANG, DEMIN · 2017 to 2024
$4.8M
An in vitro diagnostic assay for the early and accurate detection of platelet-activating antibodies associated with Heparin-inducedThrombocytopeniaR44HL147734 · NHLBI · RETHAM TECHNOLOGIES, INC. · PI Curtis Jones · 2022 to 2026
$4.6M
Molecular Basis of the Humoral Immune Response in Heparin-Induced ThrombocytopeniaR01HL148120 · NHLBI · VERSITI WISCONSIN, INC. · PI Renren Wen · 2019 to 2026
$3.8M
New approaches to the pathophysiology, diagnosis and management of heparin-induced thrombocytopeniaR01HL158932 · NHLBI · MAYO CLINIC ROCHESTER · PI PADMANABHAN, ANAND · 2021 to 2025
$2.0M
The role of proteoglycans in Heparin-induced thrombocytopenia: Implications for pathophysiology, diagnosis and treatmentK99HL171911 · NHLBI · MAYO CLINIC ROCHESTER · PI KANACK, ADAM J · 2024 to 2025
$332k
Determinants of Pathogenic Anti-PF4 Antibody-Mediated Platelet Activationathophysiology, diagnosis and treatmentR00HL171911 · NHLBI · MAYO CLINIC ARIZONA · PI Adam J Kanack · 2026 to 2026
$249k
NHLBI NIH HHS K99 HL171911NHLBI NIH HHS P01 HL167668NHLBI NIH HHS R00 HL171911NHLBI NIH HHS R01 HL130724NHLBI NIH HHS R01 HL148120NHLBI NIH HHS R01 HL158932NHLBI NIH HHS R44 HL147734
6 · The paper itself

Abstract

backgroundPlatelet factor 4-polyanion enzyme-linked immunosorbent assays (ELISAs) are considered highly sensitive for diagnosing heparin-induced thrombocytopenia (HIT), such that current practice guidelines recommend use of ELISA-negative results to exclude HIT. Once HIT is ruled out, alternative, non-heparin-based anticoagulant treatments are ceased, and heparin reintroduction frequently occurs.

methodsAntigen-based and PF4-dependent functional testing were used to study PF4/polyvinyl sulfonate ELISA-negative platelet-activating antibodies in HIT-suspected patients and mice immunized with PF4/heparin.

resultsThree patients with clinical presentations consistent with HIT tested negative in an ELISA using PF4-polyvinylsulfonate (PF4/PVS), an antigenic target very commonly used for HIT antibody detection. All three patients demonstrated PF4-dependent platelet activation in functional testing that was sensitive to blockade of platelet FcγRIIa receptors and inhibited by high concentrations of heparin, consistent with pathogenic HIT antibodies. Functional testing-based screening of 500 ELISA-negative patients identified three patients whose sera activated platelets in a PF4- and FcγRIIa-dependent manner, and had clinical histories consistent with HIT. Five of the six ELISA-negative HIT patients were re-exposed to heparin, which precipitated a decrease in platelet counts in all re-exposed patients, and one patient developed a new thrombus. To advance the study of ELISA-negative HIT antibodies, mice were immunized with PF4/heparin, and functional and antigenic assays were simultaneously used to successfully identify an ELISA-negative, PF4-dependent platelet-activating murine monoclonal antibody that recapitulated the serological characteristics of ELISA-negative HIT patients.

conclusionsRecognition of ELISA-negative HIT is critical to avoid harm due to the cessation of alternative anticoagulation therapy and re-exposure of these patients to heparin.

Identifiers

PMID41282766
PMCPMC12637735

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