Evidence map›Paper›PMID 39309228›Full record

ArticleResearch and practice in thrombosis and haemostasis2024

Antipolyphosphate monoclonal antibodies derived from autoimmune mice.

Josepha C Sedzro, Stephanie A Smith, Alexander Scott, Yuqi Wang, Richard J Travers, Rachel Hemp, Chase N Morse, James H Morrissey

Abstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Josepha C SedzroDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Stephanie A SmithDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Alexander ScottDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Yuqi WangDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Richard J TraversDepartment of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Rachel HempDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Chase N MorseDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan, USA.
James H MorrisseyDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan, USA.

Funding

Analysis and Characterization of Trauma-Induced CoagulopathyUM1HL120877 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI MORRISSEY, JAMES H., WISNIEWSKI, STEPHEN R · 2013 to 2019
$26.6M
Mechanisms in Blood ClottingR35HL135823 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORRISSEY, JAMES H. · 2017 to 2023
$4.8M
Mechanisms in Blood ClottingR35HL171334 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI James H. Morrissey · 2024 to 2026
$2.9M
NHLBI NIH HHS R35 HL135823NHLBI NIH HHS R35 HL171334NHLBI NIH HHS UM1 HL120877
6 · The paper itself

Abstract

Background: Inorganic polyphosphates (polyPs) are linear chains of phosphates that accelerate blood clotting. Targeting polyP Objectives: To identify and characterize anti-polyP monoclonal antibodies that could be used as analytical tools and as antithrombotic agents. Methods: Hybridomas were prepared from spleen cells from autoimmune NZBWF1/J female mice and screened for anti-polyP antibodies. Antibodies that bound polyP using enzyme-linked immunosorbent assay and pull-down assays were further characterized with plate binding, surface plasmon resonance, and plasma-based clotting assays. Antithrombotic potential was evaluated in a murine ferric chloride-induced carotid artery thrombosis model. Results: Of 4 antibodies that bound polyP in our pull-down assay, 2 (PP2069 and PP2099) were available for further characterization. While analyzing these anti-polyP antibodies, we found secretory leukocyte peptidase inhibitor (SLPI) to be a common contaminant of these antibodies and that SLPI binds polyP. We removed SLPI quantitatively from our purified immunoglobulin G. Both PP2069 and PP2099 immunoglobulin G displayed high affinity for polyP but also bound to other polyanions such as DNA, heparin, and certain other glycosaminoglycans, indicating limited specificity. Both antibodies inhibited polyP-initiated plasma clotting Conclusion: Autoimmune mice spontaneously produce antibodies against polyP. The 2 examples of anti-polyP monoclonal antibodies studied here not only bound to polyP with high affinity but also cross-reacted with DNA and heparin. Neither antibody protected against thrombosis in a mouse model, but they might have some utility for

Indexed as

antibodiesautoantibodiesmicemonoclonalpolyphosphatethrombosis

Identifiers

PMID39309228
PMCPMC11414566

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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.