Evidence map›Paper›PMID 30089712›Full record

ArticleJCI insight2018

Platelet-targeted dual pathway antithrombotic inhibits thrombosis with preserved hemostasis.

Donny Hanjaya-Putra, Carolyn Haller, Xiaowei Wang, Erbin Dai, Bock Lim, Liying Liu, Patrick Jaminet, Joy Yao, Amy Searle, Thomas Bonnard and 3 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.9field-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

14 citing papers in PubMed, 35 citations in OpenAlex.

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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

13 authors at 3 institutions in 3 countries.

Donny Hanjaya-PutraDepartment of Surgery, Beth Israel Deaconess Medical Center (BIDMC), Harvard Medical School, Boston, Massachusetts, USA.
Carolyn HallerDepartment of Surgery, Beth Israel Deaconess Medical Center (BIDMC), Harvard Medical School, Boston, Massachusetts, USA.
Xiaowei WangBaker Heart and Diabetes Research Institute, Melbourne, VIC 8008, Australia.
Erbin DaiDepartment of Surgery, Beth Israel Deaconess Medical Center (BIDMC), Harvard Medical School, Boston, Massachusetts, USA.
Bock LimBaker Heart and Diabetes Research Institute, Melbourne, VIC 8008, Australia.
Liying LiuDepartment of Surgery, Beth Israel Deaconess Medical Center (BIDMC), Harvard Medical School, Boston, Massachusetts, USA.
Patrick JaminetUniversity Hospital, Freiburg, Germany.
Joy YaoBaker Heart and Diabetes Research Institute, Melbourne, VIC 8008, Australia.
Amy SearleBaker Heart and Diabetes Research Institute, Melbourne, VIC 8008, Australia.
Thomas BonnardBaker Heart and Diabetes Research Institute, Melbourne, VIC 8008, Australia.
Christoph E HagemeyerBaker Heart and Diabetes Research Institute, Melbourne, VIC 8008, Australia.
Karlheinz PeterBaker Heart and Diabetes Research Institute, Melbourne, VIC 8008, Australia.
Elliot L ChaikofDepartment of Surgery, Beth Israel Deaconess Medical Center (BIDMC), Harvard Medical School, Boston, Massachusetts, USA.
Baker Heart and Diabetes Institute · AUBeth Israel Deaconess Medical Center · USUniversity Medical Center Freiburg · DE

Funding

A PSGL-1 Glycopeptide Mimetic for Treatment of Venous ThromboembolismR01HL128237 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CHAIKOF, ELLIOT · 2015 to 2018
$1.7M
NHLBI NIH HHS R01 HL128237
6 · The paper itself

Abstract

Despite advances in antithrombotic therapy, the risk of recurrent coronary/cerebrovascular ischemia or venous thromboembolism remains high. Dual pathway antithrombotic blockade, using both antiplatelet and anticoagulant therapy, offers the promise of improved thrombotic protection; however, widespread adoption remains tempered by substantial risk of major bleeding. Here, we report a dual pathway therapeutic capable of site-specific targeting to activated platelets and therapeutic enrichment at the site of thrombus growth to allow reduced dosing without compromised antithrombotic efficacy. We engineered a recombinant fusion protein, SCE5-TAP, which consists of a single-chain antibody (SCE5) that targets and blocks the activated GPIIb/IIIa complex, and tick anticoagulant peptide (TAP), a potent direct inhibitor of activated factor X (FXa). SCE5-TAP demonstrated selective platelet targeting and inhibition of thrombosis in murine models of both carotid artery and inferior vena cava thrombosis, without a significant impact on hemostasis. Selective targeting to activated platelets provides an attractive strategy to achieve high antithrombotic efficacy with reduced risk of bleeding complications.

Indexed as

AnimalsArthropod ProteinsBlood PlateletsDisease Models, AnimalFactor Xa InhibitorsHealthy VolunteersHemostasisHumansImmunoconjugatesIntercellular Signaling Peptides and ProteinsMicePlatelet ActivationRecombinant Fusion ProteinsSingle-Chain AntibodiesThrombosisArthropod ProteinsFactor Xa InhibitorsImmunoconjugatesIntercellular Signaling Peptides and ProteinsRecombinant Fusion ProteinsSingle-Chain Antibodiestick anticoagulant peptideCardiologyHematologyPharmacologyPlateletsThrombosis

Identifiers

PMID30089712
PMCPMC6129120
OpenAlexW2885094357

What OpenQuestion holds

Textmetadata
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.