Evidence map›Paper›PMID 34049875›Full record

ArticleScience advances2021

Tissue-engineered vascular microphysiological platform to study immune modulation of xenograft rejection.

Tae Hee Kim, Ji-Jing Yan, Joon Young Jang, Gwang-Min Lee, Sun-Kyung Lee, Beom Seok Kim, Justin J Chung, Soo Hyun Kim, Youngmee Jung, Jaeseok Yang

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Vascular microphysiological systems.Current opinion in hematology · 2024
    Review
  4. Article
  5. Review
  6. 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

10 authors at 4 institutions in 1 country.

Tae Hee KimCenter for Biomaterials, Biomedical Research Institute, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.ORCID 0000-0002-3862-6610
Ji-Jing YanBiomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0002-4048-1406
Joon Young JangBiomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0003-2372-1161
Gwang-Min LeeBiomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.
Sun-Kyung LeeBiomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0003-0311-7709
Beom Seok KimDivision of Nephrology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-5732-2583
Justin J ChungCenter for Biomaterials, Biomedical Research Institute, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
Soo Hyun KimCenter for Biomaterials, Biomedical Research Institute, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.ORCID 0000-0002-8391-3686
Youngmee JungCenter for Biomaterials, Biomedical Research Institute, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea. jcyjs@snu.ac.kr winnie97@kist.re.kr.ORCID 0000-0002-4778-4629
Jaeseok YangBiomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea. jcyjs@snu.ac.kr winnie97@kist.re.kr.ORCID 0000-0002-5378-7797
Korea Institute of Science and Technology · KRSeoul National University Hospital · KRSeoul National University · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most of the vascular platforms currently being studied are lab-on-a-chip types that mimic capillary networks and are applied for vascular response analysis in vitro. However, these platforms have a limitation in clearly assessing the physiological phenomena of native blood vessels compared to in vivo evaluation. Here, we developed a simply fabricable tissue-engineered vascular microphysiological platform (TEVMP) with a three-dimensional (3D) vascular structure similar to an artery that can be applied for ex vivo and in vivo evaluation. Furthermore, we applied the TEVMP as ex vivo and in vivo screening systems to evaluate the effect of human CD200 (hCD200) overexpression in porcine endothelial cells (PECs) on vascular xenogeneic immune responses. These screening systems, in contrast to 2D in vitro and cellular xenotransplantation in vivo models, clearly demonstrated that hCD200 overexpression effectively suppressed vascular xenograft rejection. The TEVMP has a high potential as a platform to assess various vascular-related responses.

Identifiers

PMID34049875
PMCPMC8163083
OpenAlexW3164445443

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.