Evidence map›Paper›PMID 31590323›Full record

ArticleJournal of clinical medicine2019

A Virus-Derived Immune Modulating Serpin Accelerates Wound Closure with Improved Collagen Remodeling.

Liqiang Zhang, Jordan R Yaron, Amanda M Tafoya, Sarah E Wallace, Jacquelyn Kilbourne, Shelley Haydel, Kaushal Rege, Grant McFadden, Alexandra R Lucas

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

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  14. RecombinantPharmaceutics · 2020
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  18. A Macrophage-Based Cell Therapy Approach Promotes Collagen Deposition in Diabetic Wounds.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    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

9 authors at 2 institutions in 1 country.

Liqiang ZhangCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA. liqiang.zhang@asu.edu.
Jordan R YaronCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA. jyaron@asu.edu.
Amanda M TafoyaCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA. agonza49@asu.edu.
Sarah E WallaceCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA. 789sew@gmail.com.
Jacquelyn KilbourneCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA. Jacki.Kilbourne@asu.edu.
Shelley HaydelCenter for Bioelectronics and Biosensors, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA. Shelley.Haydel@asu.edu.
Kaushal RegeChemical Engineering, Arizona State University, Tempe, AZ 85287, USA. Kaushal.Rege@asu.edu.
Grant McFaddenCenter for Immunotherapy, Vaccines and Virotherapy, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA. grantmcf@asu.edu.
Alexandra R LucasCenter for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA. arlucas5@asu.edu.
Arizona State University · USBioElectronics (United States) · US

Funding

NIH HHS 1RC1HL100202
6 · The paper itself

Abstract

Numerous treatments have been developed to promote wound healing based on current understandings of the healing process. Hemorrhaging, clotting, and associated inflammation regulate early wound healing. We investigated treatment with a virus-derived immune modulating serine protease inhibitor (SERPIN), Serp-1, which inhibits thrombolytic proteases and inflammation, in a mouse excisional wound model. Saline or recombinant Serp-1 were applied directly to wounds as single doses of 1 μg or 2 µg or as two 1 µg boluses. A chitosan-collagen hydrogel was also tested for Serp-1 delivery. Wound size was measured daily for 15 days and scarring assessed by Masson's trichrome, Herovici's staining, and immune cell dynamics and angiogenesis by immunohistochemistry. Serp-1 treatment significantly accelerated wound healing, but was blocked by urokinase-type plasminogen activator (uPAR) antibody. Repeated dosing at a lower concentration was more effective than single high-dose serpin. A single application of Serp-1-loaded chitosan-collagen hydrogel was as effective as repeated aqueous Serp-1 dosing. Serp-1 treatment of wounds increased arginase-1-expressing M2-polarized macrophage counts and periwound angiogenesis in the wound bed. Collagen staining also demonstrated that Serp-1 improves collagen maturation and organization at the wound site. Serp-1 has potential as a safe and effective immune modulating treatment that targets thrombolytic proteases, accelerating healing and reducing scar in deep cutaneous wounds.

Indexed as

hydrogelimmune modulationscarringserpinwound healing

Identifiers

PMID31590323
PMCPMC6832452
OpenAlexW2979171250

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.