Evidence map›Paper›PMID 35160081›Full record

ArticleJournal of clinical medicine2022

Plasma-Derived Hemopexin as a Candidate Therapeutic Agent for Acute Vaso-Occlusion in Sickle Cell Disease: Preclinical Evidence.

Thomas Gentinetta, John D Belcher, Valérie Brügger-Verdon, Jacqueline Adam, Tanja Ruthsatz, Joseph Bain, Daniel Schu, Lisa Ventrici, Monika Edler, Hadi Lioe and 19 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.4field-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

26 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  6. Acellular Hemoglobin Impairs Cardiomyocyte Excitation-Contraction Coupling.ASAIO journal (American Society for Artificial Internal Organs : 1992) · 2026
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  10. Review
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  15. Review
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  17. Understanding mechanisms of antioxidant action in health and disease.Nature reviews. Molecular cell biology · 2024
    Review
  18. Article
  19. Article
  20. Accelerated atherosclerosis in beta-thalassemia.American journal of physiology. Heart and circulatory physiology · 2023
    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

29 authors at 5 institutions in 4 countries.

Thomas GentinettaResearch and Development, CSL Behring AG, 3014 Bern, Switzerland.
John D BelcherDivision of Hematology, Oncology and Transplantation, Vascular Biology Center, Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.
Valérie Brügger-VerdonResearch and Development, CSL Behring AG, 3014 Bern, Switzerland.ORCID 0000-0001-6009-6719
Jacqueline AdamResearch and Development, CSL Behring AG, 3014 Bern, Switzerland.
Tanja RuthsatzCSL Behring Innovation GmbH, 35041 Marburg, Germany.
Joseph BainCSL Behring Innovation GmbH, 35041 Marburg, Germany.
Daniel SchuCSL Behring Innovation GmbH, 35041 Marburg, Germany.
Lisa VentriciResearch and Development, CSL Behring AG, 3014 Bern, Switzerland.
Monika EdlerResearch and Development, CSL Behring AG, 3014 Bern, Switzerland.
Hadi LioeBio21 Institute, CSL Ltd., Parkville, VIC 3052, Australia.
Kalpeshkumar PatelBio21 Institute, CSL Ltd., Parkville, VIC 3052, Australia.
Chunsheng ChenDivision of Hematology, Oncology and Transplantation, Vascular Biology Center, Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.
Julia NguyenDivision of Hematology, Oncology and Transplantation, Vascular Biology Center, Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.
Fuad AbdullaDivision of Hematology, Oncology and Transplantation, Vascular Biology Center, Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.
Ping ZhangDivision of Hematology, Oncology and Transplantation, Vascular Biology Center, Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.
Andreas WassmerResearch and Development, CSL Behring AG, 3014 Bern, Switzerland.
Meena JainResearch and Development, CSL Behring, King of Prussia, PA 19406, USA.
Marcel MischnikCSL Behring Innovation GmbH, 35041 Marburg, Germany.
Matthias PelzingBio21 Institute, CSL Ltd., Parkville, VIC 3052, Australia.
Kirstee MartinBio21 Institute, CSL Ltd., Parkville, VIC 3052, Australia.
Roslyn DavisBio21 Institute, CSL Ltd., Parkville, VIC 3052, Australia.
Svetlana DidichenkoResearch and Development, CSL Behring AG, 3014 Bern, Switzerland.
Alexander SchaubResearch and Development, CSL Behring AG, 3014 Bern, Switzerland.
Nathan BrinkmanResearch and Development, CSL Behring Ltd., Kankakee, IL 60901, USA.
Eva HerzogResearch and Development, CSL Behring, King of Prussia, PA 19406, USA.
Adrian ZürcherResearch and Development, CSL Behring AG, 3014 Bern, Switzerland.
Gregory M VercellottiDivision of Hematology, Oncology and Transplantation, Vascular Biology Center, Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.
Gregory J KatoResearch and Development, CSL Behring, King of Prussia, PA 19406, USA.ORCID 0000-0003-4465-3217
Gerald HöbarthCSL Behring GmbH, Walcherstraße 1A/Stiege 1, 1020 Vienna, Austria.
CSL (Switzerland) · CHUniversity of Minnesota · USCSL (Australia) · AUBehringwerke (Germany) · DECSL (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

People living with sickle cell disease (SCD) face intermittent acute pain episodes due to vaso-occlusion primarily treated palliatively with opioids. Hemolysis of sickle erythrocytes promotes release of heme, which activates inflammatory cell adhesion proteins on endothelial cells and circulating cells, promoting vaso-occlusion. In this study, plasma-derived hemopexin inhibited heme-mediated cellular externalization of P-selectin and von Willebrand factor, and expression of IL-8, VCAM-1, and heme oxygenase-1 in cultured endothelial cells in a dose-responsive manner. In the Townes SCD mouse model, intravenous injection of free hemoglobin induced vascular stasis (vaso-occlusion) in nearly 40% of subcutaneous blood vessels visualized in a dorsal skin-fold chamber. Hemopexin administered intravenously prevented or relieved stasis in a dose-dependent manner. Hemopexin showed parallel activity in relieving vascular stasis induced by hypoxia-reoxygenation. Repeated IV administration of hemopexin was well tolerated in rats and non-human primates with no adverse findings that could be attributed to human hemopexin. Hemopexin had a half-life in wild-type mice, rats, and non-human primates of 80-102 h, whereas a reduced half-life of hemopexin in Townes SCD mice was observed due to ongoing hemolysis. These data have led to a Phase 1 clinical trial of hemopexin in adults with SCD, which is currently ongoing.

Indexed as

hemehemoglobinhemopexinsickle cell anaemiavaso-occlusive crisis

Identifiers

PMID35160081
PMCPMC8836474
OpenAlexW4210339565

What OpenQuestion holds

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Registered trials

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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.