Evidence map›Paper›PMID 40564144›Full record

ReviewBiomedicines2025

Unraveling the Roles of Macrophages in Vascularized Composite Allotransplantation.

Hui-Yun Cheng, Madonna Rica Anggelia, Cheng-Hung Lin

Abstract readReview
In one paragraph

Review in Biomedicines, 2025. 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. Chronic Rejection in Facial Vascularized Composite Allotransplantation (fVCA).Results and problems in cell differentiation · 2026
    Review
  2. Review
  3. 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

3 authors.

Hui-Yun ChengCenter for Vascularized Composite Allotransplantation, Chang Gung Memorial Hospital at Linkou, Kweishan, Taoyuan 333, Taiwan.ORCID 0000-0001-5422-2598
Madonna Rica AnggeliaDepartment of Plastic and Reconstructive Surgery, Chang Gung Memorial Hospital at Linkou, Kweishan, Taoyuan 333, Taiwan.ORCID 0000-0002-6139-8505
Cheng-Hung LinCenter for Vascularized Composite Allotransplantation, Chang Gung Memorial Hospital at Linkou, Kweishan, Taoyuan 333, Taiwan.ORCID 0000-0001-7278-093X

Funding

National Science and Technology Council Taiwan MOST 111-2314-B-182A-121-MY3
6 · The paper itself

Abstract

The phenotypic heterogeneity and functional diversity of macrophages have been increasingly appreciated, particularly regarding their roles as innate immune cells in shaping transplantation outcomes. However, their functions in vascularized composite allotransplantation (VCA) remain underexplored. In this review, we first describe the development of macrophages and the heterogeneity of macrophage differentiation, then present current insights into macrophages' involvement across key stages of VCA, including ischemia-reperfusion injury at the peri-transplantation stage, and the outcomes following transplantation, including acute rejection, chronic rejection, and development of transplantation tolerance. The existing evidence supports that macrophages significantly influence both short- and long-term VCA graft survival. The presence of vascularized bone marrow within some VCA grafts further suggests the involvement of donor bone marrow-derived macrophage population and adds another layer of complexity to immune dynamics. Collectively, current understanding highlights the macrophage as a promising target for therapeutic intervention and warrants continued investigation into their diverse functions and potential for improving VCA outcomes.

Indexed as

ischemia–reperfusion injuryM1 macrophageM2 macrophagemacrophageregulatory macrophagetransplantation rejectiontransplantation tolerancevascularized composite allotransplantation

Identifiers

PMID40564144
PMCPMC12189788

What OpenQuestion holds

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LicenceCC BY
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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.