Evidence map›Paper›PMID 41263118›Full record

ArticleAdvanced biology2026

Lung Microphysiological System Validates Novel Cell Therapy for Acute Respiratory Distress Syndrome.

Bokyong Kim, So-Hui Kim, Jieun Kim, Eun-Young Eo, Hyung-Jun Kim, Jae Ho Lee, Choon-Taek Lee, Taeho Kong, Su Kyoung Seo, Seunghee Lee and 2 more

Abstract read
In one paragraph

Article in Advanced biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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

12 authors.

Bokyong KimDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-ro 173 Beon-gil, Bundang-gu, Seongnam-si, Gyeonggi-do, 13620, Republic of Korea.ORCID 0000-0002-1326-5206
So-Hui KimSchool of Biomedical Convergence Engineering, Pusan National University, Busandaehak-ro 49 Beon-gil, Yangsan-si, Gyeongsangnam-do, 50612, Republic of Korea.ORCID 0009-0002-3319-422X
Jieun KimDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-ro 173 Beon-gil, Bundang-gu, Seongnam-si, Gyeonggi-do, 13620, Republic of Korea.ORCID 0009-0001-8992-4060
Eun-Young EoDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-ro 173 Beon-gil, Bundang-gu, Seongnam-si, Gyeonggi-do, 13620, Republic of Korea.ORCID 0000-0001-8656-3733
Hyung-Jun KimDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-ro 173 Beon-gil, Bundang-gu, Seongnam-si, Gyeonggi-do, 13620, Republic of Korea.ORCID 0000-0003-1984-8864
Jae Ho LeeDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-ro 173 Beon-gil, Bundang-gu, Seongnam-si, Gyeonggi-do, 13620, Republic of Korea.ORCID 0000-0002-4766-1231
Choon-Taek LeeDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-ro 173 Beon-gil, Bundang-gu, Seongnam-si, Gyeonggi-do, 13620, Republic of Korea.ORCID 0000-0001-8030-3332
Taeho KongStem Cell and Regenerative Bioengineering Institute, Global R&D Center, Kangstem Biotech Co., Ltd, Ace Highend Tower 8, 84, Gasan Digital 1-ro, Geumcheon-gu, Seoul, 08590, Republic of Korea.
Su Kyoung SeoStem Cell and Regenerative Bioengineering Institute, Global R&D Center, Kangstem Biotech Co., Ltd, Ace Highend Tower 8, 84, Gasan Digital 1-ro, Geumcheon-gu, Seoul, 08590, Republic of Korea.
Seunghee LeeStem Cell and Regenerative Bioengineering Institute, Global R&D Center, Kangstem Biotech Co., Ltd, Ace Highend Tower 8, 84, Gasan Digital 1-ro, Geumcheon-gu, Seoul, 08590, Republic of Korea.
Jeongbin ParkSchool of Biomedical Convergence Engineering, Pusan National University, Busandaehak-ro 49 Beon-gil, Yangsan-si, Gyeongsangnam-do, 50612, Republic of Korea.ORCID 0000-0002-9064-4912
Young-Jae ChoDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, 82, Gumi-ro 173 Beon-gil, Bundang-gu, Seongnam-si, Gyeonggi-do, 13620, Republic of Korea.ORCID 0000-0001-6943-4462

Funding

Korean government (the Ministry of Health and Welfare) KFRM 21C0710S1-21Korean government (the Ministry of Science and ICT) RS-2024-00439078
6 · The paper itself

Abstract

Acute Respiratory Distress Syndrome (ARDS) is a life-threatening condition characterized by severe inflammation and lung damage, leading to critical hypoxemia. Despite its high mortality rate, the only currently available treatment, Dexamethasone, is associated with significant side effects. This study aims to evaluate the efficacy of primed human umbilical cord blood-derived mesenchymal stem cells (hUCB-pMSCs) as a potential alternative treatment for ARDS. A novel lung microphysiological system (MPS) modeling the lung environment is developed and treated with lipopolysaccharide (LPS) to simulate ARDS. The effects of hUCB-pMSCs and dexamethasone are compared using state-of-the-art methods, including fluorescence-based imaging and single-cell RNA sequencing. The hUCB-pMSCs significantly activated angiogenesis-related pathways in endothelial cells and enhanced the formation of tip-like endothelial cells involved in new blood vessel formation. These findings are corroborated by fluorescence microscopy, demonstrating the robust potential of hUCB-pMSCs as a therapeutic approach. Overall, the results support the potential of hUCB-pMSCs as a promising alternative treatment for ARDS.

Indexed as

Cell- and Tissue-Based TherapyLungMesenchymal Stem CellsMesenchymal Stem Cell TransplantationRespiratory Distress SyndromeCells, CulturedDexamethasoneFetal BloodHumansLipopolysaccharidesMicrophysiological SystemsDexamethasoneLipopolysaccharidesacute respiratory distress syndromeendotheliummesenchymal stem cellsmicrophysiological systemtranslational research

Identifiers

PMID41263118
PMCPMC12789962

What Socratic 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 Socratic graph.