Evidence map›Paper›PMID 30312535›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2019

Chronic rejection of human face allografts.

Nicco Krezdorn, Christine G Lian, Michael Wells, Luccie Wo, Sotirios Tasigiorgos, Shuyun Xu, Thiago J Borges, Rayven M Frierson, Ewelina Stanek, Leonardo V Riella and 2 more

Open access · hybridAbstract read
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
5.4field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 76 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Article
  7. Chronic Rejection in Facial Vascularized Composite Allotransplantation (fVCA).Results and problems in cell differentiation · 2026
    Review
  8. Ten-year follow-up after face transplantation-A single-center retrospective cohort study.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Autologous Tissue Repair and Total Face Restoration.JAMA otolaryngology-- head & neck surgery · 2024
    Article
  14. Article
  15. International consensus recommendations on face transplantation: A 2-step Delphi study.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2024
    Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

12 authors at 1 institution in 2 countries.

Nicco KrezdornDivision of Plastic Surgery, Department of Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-2662-6290
Christine G LianProgram in Dermatopathology, Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Michael WellsProgram in Dermatopathology, Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Luccie WoDivision of Plastic Surgery, Department of Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Sotirios TasigiorgosDivision of Plastic Surgery, Department of Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0001-6826-8503
Shuyun XuProgram in Dermatopathology, Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Thiago J BorgesTransplant Research Center, Renal Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Rayven M FriersonProgram in Dermatopathology, Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Ewelina StanekProgram in Dermatopathology, Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Leonardo V RiellaTransplant Research Center, Renal Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Bohdan PomahacDivision of Plastic Surgery, Department of Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
George F MurphyProgram in Dermatopathology, Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Brigham and Women's Hospital · US

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
Cellular Pathology of Graft Versus Host DiseaseR01HL084815 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MURPHY, GEORGE F · 2006 to 2010
$1.5M
NCRR NIH HHS UL1 RR025758NHLBI NIH HHS R01 HL084815U.S. Department of Defense #W911QY-09-C-0216
6 · The paper itself

Abstract

Face vascularized composite allografts (FVCAs) have helped patients with severe facial disfigurement, with acute rejection now largely controlled through iatrogenic immunosuppression. However, little is known regarding the incidence and mechanism(s) of more long-term pathologic alterations in FVCAs that may affect function and graft durability. Protocol surveillance biopsy specimens for up to an 8-year interval in 7 patients who received FVCAs at our institution revealed histopathologic evidence of chronic rejection. Clinical manifestations included features of premature aging, mottled leukoderma accentuating suture lines, telangiectasia, and dryness of nasal mucosa. Pathologic changes consisted of epidermal thinning accompanied by discrete foci of lymphocyte-mediated cytotoxicity, hyperkeratosis, follicular plugging, vascular ectasia, and sclerosis beneath the epidermal layer associated with collagen type I deposition. Genomic interrogation and immunohistochemistry of sclerotic zones revealed upregulation of the AP-1 pathway components, JunB and c-Fos, previously implicated in overproduction of type I dermal collagen in the setting of systemic sclerosis. We conclude that some patients develop chronic rejection in FVCAs with striking similarities to alterations seen in certain autoimmune cutaneous disorders (lupus erythematosus and scleroderma/chronic sclerodermoid graft-versus-host disease). Identification of relevant pathways and genes, such as JunB and c-Fos, may provide new targets for preventative therapies for chronic immune-mediated changes in vascularized composite allografts.

Indexed as

Graft RejectionAdultChronic DiseaseComposite Tissue AllograftsFacial TransplantationFemaleGene Expression ProfilingHumansImmunosuppressive AgentsMaleMiddle AgedImmunosuppressive Agentsclinical research/practicefibrosisgenomicsimmunohistochemistrymolecular biology: mRNA/mRNA expressionpathology/histopathologyrejection: chronicvascularized composite and reconstructive transplantation

Identifiers

PMID30312535
PMCPMC6433509
OpenAlexW2897822162

What OpenQuestion holds

Textmetadata
LicenceTDM
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.