Evidence map›Paper›PMID 42681409›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Anti-platelet Factor 4/Heparin Antibody Production in a Mouse Immunization Model.

Mei Yu, Renren Wen, Demin Wang

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Mei YuVersiti Blood Research Institute, Milwaukee, WI, USA.
Renren WenVersiti Blood Research Institute, Milwaukee, WI, USA.
Demin WangVersiti Blood Research Institute, Milwaukee, WI, USA. DWang@Versiti.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heparin-induced thrombocytopenia (HIT) is the most prevalent form of drug-induced, immune-mediated thrombocytopenia. It involves the production of antibodies that target platelet factor 4 (PF4) in complex with heparin, leading to platelet activation. The pathogenesis of HIT is not fully understood, primarily due to the limitations of studying human patients. To bridge this gap and gain a deeper understanding of the mechanisms behind HIT antibody generation, researchers developed a murine model using immunization with mouse PF4 (mPF4)/heparin complexes. Here, we provide a detailed methodology for inducing mPF4/heparin antibodies in C57BL/6 mice and validating the immunization process. Through these techniques, we identified the critical subset of B cells responsible for producing mPF4/heparin-specific antibodies, as well as other immune cells essential for regulating this production. This immunization-based mouse model of HIT is a valuable tool for studying the immunopathogenesis of the condition.

Indexed as

AntibodiesAntibody FormationHeparinImmunizationPlatelet Factor 4ThrombocytopeniaAnimalsB-LymphocytesDisease Models, AnimalHumansMiceMice, Inbred C57BLAntibodiesHeparinPlatelet Factor 4Heparin-induced thrombocytopeniaMouse modelPlatelet factor 4/heparin-specific antibody

Identifiers

What OpenQuestion holds

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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.