Evidence map›Paper›PMID 39535214›Full record

ArticleThe Journal of infectious diseases2025

An Antimicrobial Blue Light Prototype Device Controls Infected Wounds in a Preclinical Porcine Model.

Laisa Bonafim Negri, William Farinelli, Sandeep Korupolu, Ying Wang, Yara Mannaa, Hang Lee, Jie Hui, Pu-Ting Dong, Andrea Slate, Joshua Tam and 3 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. 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

13 authors.

Laisa Bonafim NegriWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0001-9365-0763
William FarinelliWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0003-0972-485X
Sandeep KorupoluWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0009-0004-7650-9396
Ying WangWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Yara MannaaWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Hang LeeMassachusetts General Hospital, Department of Dermatology, Boston, Massachusetts, USA.ORCID 0000-0002-3498-236X
Jie HuiWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Pu-Ting DongThe ADA Forsyth Institute, Center for Comparative Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0003-2818-2021
Andrea SlateCenter for Comparative Medicine, Massachusetts Institute of Technology, Boston, USA.
Joshua TamWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-1649-3888
R Rox AndersonWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Seok-Hyun Andy YunWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Jeffrey A GelfandWellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-4118-5676

Funding

Harvard Clinical and Translational Science CenterUM1TR004408 · NCATS · HARVARD MEDICAL SCHOOL · PI Lindsey Robert Baden, Lee Marshall Nadler · 2023 to 2026
$43.3M
Differentiation of Microbe-microbe Interactions at Single-cell Level Through Unconventional Utilization of Expansion MicroscopyK99DE033794 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI DONG, PU-TING · 2024 to 2025
$324k
Edmund C. Lynch, Jr Research FundHarvard UniversityNCATS NIH HHS UM1 TR004408NIDCR NIH HHS K99 DE033794NIH HHS UM1TR004408
6 · The paper itself

Abstract

We developed a translational prototype antimicrobial blue light (ABL) device for treating skin wounds with ABL. Partial-thickness surgical wounds were created in live swine (an animal whose skin is considered the most like human skin), then heavily contaminated and left untreated for 24 hours with methicillin-resistant Staphylococcus aureus (MRSA). ABL treatment stabilized and reduced MRSA infection by greater than 4 orders of magnitude (>99.99%; P < .0001) compared with untreated wounds in the same animal, after only 2 daily treatments. These data support further development of such devices for controlling infection in skin wounds. ABL, with or without concomitant administration of negative pressure, antimicrobials, or photosensitizers, could play an important role in modern wound care by reducing the amount, duration, and cost of antibiotics needed, helping reduce antimicrobial resistance. No such device for treating human cutaneous wounds currently exists. This deserves further development and study.

Indexed as

LightMethicillin-Resistant Staphylococcus aureusPhototherapyStaphylococcal InfectionsWound InfectionAnimalsBlue LightDisease Models, AnimalSwineantimicrobial blue lightantimicrobial resistancephototherapyStaphylococcus aureus; MRSAwound infection

Identifiers

PMID39535214
PMCPMC11911787

What OpenQuestion holds

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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.