Evidence map›Paper›PMID 36258234›Full record

ArticleBiomaterials research2022

Implantable micro-scale LED device guided photodynamic therapy to potentiate antitumor immunity with mild visible light.

Jiwoong Choi, Il Seong Lee, Ju Seung Lee, Sangmin Jeon, Wan Su Yun, Suah Yang, Yujeong Moon, Jinseong Kim, Jeongrae Kim, Seunghwan Choy and 4 more

Open access · goldAbstract read
In one paragraph

Article in Biomaterials research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Biomedical optics express · 2026
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  10. Bioluminescent Systems for Theranostic Applications.International journal of molecular sciences · 2024
    Review
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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

14 authors at 5 institutions in 1 country.

Jiwoong Choi *Medicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Hwarangno 14-gil 5, Seongbuk-gu, 02792, Seoul, Republic of Korea.
Il Seong Lee *Medicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Hwarangno 14-gil 5, Seongbuk-gu, 02792, Seoul, Republic of Korea.
Ju Seung Lee *School of Chemical Engineering, Sungkyunkwan University (SKKU), 16419, Suwon, Republic of Korea.
Sangmin JeonMedicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Hwarangno 14-gil 5, Seongbuk-gu, 02792, Seoul, Republic of Korea.
Wan Su YunMedicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Hwarangno 14-gil 5, Seongbuk-gu, 02792, Seoul, Republic of Korea.
Suah YangMedicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Hwarangno 14-gil 5, Seongbuk-gu, 02792, Seoul, Republic of Korea.
Yujeong MoonMedicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Hwarangno 14-gil 5, Seongbuk-gu, 02792, Seoul, Republic of Korea.
Jinseong KimMedicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Hwarangno 14-gil 5, Seongbuk-gu, 02792, Seoul, Republic of Korea.
Jeongrae KimMedicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Hwarangno 14-gil 5, Seongbuk-gu, 02792, Seoul, Republic of Korea.
Seunghwan ChoyDivision of Digital Clinical Research, Korea Institute of Oriental Medicine (KIOM), 1672 Yuseongdae-ro, Yuseong-gu, Daejeon, Republic of Korea.
Chanho JeongDepartment of Biomedical Engineering, Sungkyunkwan University (SKKU), 16419, Suwon, Republic of Korea.
Man Kyu ShimMedicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Hwarangno 14-gil 5, Seongbuk-gu, 02792, Seoul, Republic of Korea. mks@kist.re.kr.
Tae-Il KimSchool of Chemical Engineering, Sungkyunkwan University (SKKU), 16419, Suwon, Republic of Korea. taeilkim@skku.edu.
Kwangmeyung KimMedicinal Materials Research Center, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Hwarangno 14-gil 5, Seongbuk-gu, 02792, Seoul, Republic of Korea. kimkm@ewha.ac.kr.ORCID http://orcid.org/0000-0001-7919-188X
Korea University · KRSungkyunkwan University · KRKorea Institute of Science and Technology · KREwha Womans University · KRKorea Institute of Oriental Medicine · KR

Funding

National Research Foundation (NRF) of Korea NRF-2022M3H4A1A03067401Samsung Research Funding & Incubation Center for Future Technology of Samsung Electronics SRFC-IT1901-16
6 · The paper itself

Abstract

backgroundPhotodynamic therapy (PDT) is a promising strategy to promote antitumor immunity by inducing immunogenic cell death (ICD) in tumor cells. However, practical PDT uses an intense visible light owing to the shallow penetration depth of the light, resulting in immunosuppression at the tumor tissues.

methodsHerein, we propose an implantable micro-scale light-emitting diode device (micro-LED) guided PDT that enables the on-demand light activation of photosensitizers deep in the body to potentiate antitumor immunity with mild visible light.

resultsThe micro-LED is prepared by stacking one to four micro-scale LEDs (100 μm) on a needle-shape photonic device, which can be directly implanted into the core part of the tumor tissue. The photonic device with four LEDs efficiently elicits sufficient light output powers without thermal degradation and promotes reactive oxygen species (ROS) from a photosensitizer (verteporfin; VPF). After the intravenous injection of VPF in colon tumor-bearing mice, the tumor tissues are irradiated with optimal light intensity using an implanted micro-LED. While tumor tissues under intense visible light causes immunosuppression by severe inflammatory responses and regulatory T cell activation, mild visible light elicits potent ICD in tumor cells, which promotes dendritic cell (DC) maturation and T cell activation. The enhanced therapeutic efficacy and antitumor immunity by micro-LED guided PDT with mild visible light are assessed in colon tumor models. Finally, micro-LED guided PDT in combination with immune checkpoint blockade leads to 100% complete tumor regression and also establishes systemic immunological memory to prevent the recurrence of tumors.

conclusionCollectively, this study demonstrates that micro-LED guided PDT with mild visible light is a promising strategy for cancer immunotherapy.

Indexed as

cancer immunotherapyCell death and immune responseImmune checkpoint blockadeImplantable photonic devicePhotodynamic therapy

Identifiers

PMID36258234
PMCPMC9580183
OpenAlexW4306734838

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.