Evidence map›Paper›PMID 31730284›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2020

Recombinant human ADAMTS13 treatment and anti-NET strategies enhance skin allograft survival in mice.

Siu Ling Wong, Jeremy Goverman, Caleb Staudinger, Denisa D Wagner

Open access · hybridAbstract read
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Neutrophil extracellular traps in homeostasis and disease.Signal transduction and targeted therapy · 2024
    Review
  6. The Highs and Lows of ADAMTS13 Activity.Journal of clinical medicine · 2024
    Review
  7. Article
  8. Review
  9. Article
  10. Mechanisms of ADAMTS13 regulation.Journal of thrombosis and haemostasis : JTH · 2022
    Review
  11. Anti-inflammatory protective effect of ADAMTS-13 in murine arthritis models.Journal of thrombosis and haemostasis : JTH · 2022
    Article
  12. Thromboinflammation: From Atherosclerosis to COVID-19.Arteriosclerosis, thrombosis, and vascular biology · 2022
    Review
  13. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Siu Ling WongProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-2294-3187
Jeremy GovermanDepartment of Surgery, Massachusetts General Hospital, Shriners Hospitals for Children, Harvard Medical School, Boston, Massachusetts, USA.
Caleb StaudingerProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
Denisa D WagnerProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-4494-413X
Boston Children's Hospital · USHarvard University · US

Funding

How inflammation and thrombosis fuel disease and aging: Focus on NETsR35HL135765 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI WAGNER, DENISA D · 2017 to 2023
$6.2M
Baxalta US Inc H15-30683NHLBI NIH HHS R35 HL135765Plastic Surgeon Foundation
6 · The paper itself

Abstract

Enhancing skin allograft longevity lessens the need for new allografts before optimal intervention is available. Reduced activity of ADAMTS13 (an enzyme that cleaves the pro-thrombotic and proinflammatory von Willebrand factor) and presence of neutrophil extracellular traps (NETs) have been implicated in liver and lung allograft failures. The effect of ADAMTS13 treatment and the impact of NETs on skin allografts, however, remain unexplored. Here, we adopted a murine model of complete mismatch full-thickness skin transplant by grafting dorsal skin from BALB/c mice to C57BL/6J background mice. Recombinant human ADAMTS13 (rhADAMTS13) treatment of graft recipients increased allograft survival. Western blot and immunofluorescence microscopy revealed the presence of NETs in allografts of vehicle, but surprisingly, not in rhADAMTS13-treated mice, 3 days after surgery. Recapitulating the observations in mice, NETs were also observed in all the examined allografts from burn patients. Intriguingly, knocking out peptidylarginine deiminase 4 (PAD4, a key enzyme for NET formation) or DNase 1 treatment (which cleaves NETs) also prolonged allograft survival. In summary, rhADAMTS13 lessens inflammation in allografts by reducing NET burden, resulting in enhanced allograft survival. RhADAMTS13 and anti-NET treatments could be new therapeutic strategies to promote skin allograft longevity and, hence, the survival of patients with severe burns.

Indexed as

Graft Survivalvon Willebrand FactorADAMTS13 ProteinAllograftsAnimalsGraft RejectionHumansMiceMice, Inbred BALB CMice, Inbred C57BLTransplantation, HomologousADAMTS13 ProteinADAMTS13 protein, humanADAMTS13 protein, mousevon Willebrand Factoradhesion molecules/integrinsanimal models: murinebasic (laboratory) research/scienceimmunobiologyorgan transplantation in generalrejectionthrombolytic therapy/thrombolysistissue (nonvascularized) transplantationtranslational research/science

Identifiers

PMID31730284
PMCPMC7103495
OpenAlexW2987754376

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.