Evidence map›Paper›PMID 39310283›Full record

ArticleTransplantation direct2024

Molecular Signature Associated With Acute Rejection in Vascularized Composite Allotransplantation.

Michael F Cassidy, Nicole A Doudican, Nicholas Frazzette, Piul S Rabbani, John A Carucci, Bruce E Gelb, Eduardo D Rodriguez, Catherine P Lu, Daniel J Ceradini

Abstract read
In one paragraph

Article in Transplantation direct, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Michael F CassidyHansjörg Wyss Department of Plastic Surgery, NYU Langone Health, New York, NY.ORCID https://orcid.org/0000-0001-8763-6797
Nicole A DoudicanRonald O. Perelman Department of Dermatology, NYU Langone Health, New York, NY.
Nicholas FrazzetteRonald O. Perelman Department of Dermatology, NYU Langone Health, New York, NY.
Piul S RabbaniHansjörg Wyss Department of Plastic Surgery, NYU Langone Health, New York, NY.
John A CarucciRonald O. Perelman Department of Dermatology, NYU Langone Health, New York, NY.
Bruce E GelbTransplant Institute, NYU Langone Health, New York, NY.
Eduardo D RodriguezHansjörg Wyss Department of Plastic Surgery, NYU Langone Health, New York, NY.
Catherine P LuHansjörg Wyss Department of Plastic Surgery, NYU Langone Health, New York, NY.
Daniel J CeradiniHansjörg Wyss Department of Plastic Surgery, NYU Langone Health, New York, NY.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: A deeper understanding of acute rejection in vascularized composite allotransplantation is paramount for expanding its utility and longevity. There remains a need to develop more precise and accurate tools for diagnosis and prognosis of these allografts, as well as alternatives to traditional immunosuppressive regimens. Methods: Twenty-seven skin biopsies collected from 3 vascularized composite allotransplantation recipients, consisting of face and hand transplants, were evaluated by histology, immunohistochemistry staining, and gene expression profiling. Results: Biopsies with clinical signs and symptoms of rejection, irrespective of histopathological grading, were significantly enriched for genes contributing to the adaptive immune response, innate immune response, and lymphocyte activation. Inflammation episodes exhibited significant fold change correlations between the face and hands, as well as across patients. Immune checkpoint genes were upregulated during periods of inflammation that necessitated treatment. A gene signature consisting of Conclusions: The mechanism of vascularized composite allograft-specific inflammation and rejection appears to be conserved across different patients and skin on different anatomical sites. A concise gene signature can be utilized to ascertain graft status along with a continuous scale, providing valuable diagnostic and prognostic information to supplement current gold standards of graft evaluation.

Identifiers

PMID39310283
PMCPMC11415116

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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.