Evidence map›Paper›PMID 33550369›Full record

ArticleInteractive cardiovascular and thoracic surgery2021

Microvasculature in murine tracheal allografts after combined therapy with clopidogrel and everolimus.

Christian Heim, Annika Kuckhahn, Martina Ramsperger-Gleixner, Mark R Nicolls, Michael Weyand, Stephan M Ensminger

Open access · bronzeAbstract read
In one paragraph

Article in Interactive cardiovascular and thoracic surgery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 3 institutions in 2 countries.

Christian HeimDepartment of Cardiac Surgery, University of Erlangen-Nuremberg, Erlangen, Germany.ORCID 0000-0001-5884-5856
Annika KuckhahnDepartment of Cardiac Surgery, University of Erlangen-Nuremberg, Erlangen, Germany.
Martina Ramsperger-GleixnerDepartment of Cardiac Surgery, University of Erlangen-Nuremberg, Erlangen, Germany.
Mark R NicollsVeterans Affairs Palo Alto Health Care System/Stanford University School of Medicine, Stanford, CA, USA.
Michael WeyandDepartment of Cardiac Surgery, University of Erlangen-Nuremberg, Erlangen, Germany.
Stephan M EnsmingerDepartment of Cardiac Surgery, University of Luebeck, Luebeck, Germany.
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity of Lübeck · DEVA Palo Alto Health Care System · US

Funding

Critical Role for Microvasculature in Airway TransplantationR01HL095686 · NHLBI · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI NICOLLS, MARK ROBERT · 2010 to 2022
$4.7M
NHLBI NIH HHS R01 HL095686
6 · The paper itself

Abstract

objectivesSurvival after lung transplantation is mainly limited by the development of chronic lung allograft dysfunction. Previous studies have suggested T-cell mediated proliferation and microvascular changes in experimental small airways models as potential therapeutic targets. The aim of this study was to assess microvascular changes in murine orthotopic tracheal allografts after treatment with everolimus alone or in combination with clopidogrel.

methodsC57Bl/6 (H-2b) donor tracheas were orthotopically transplanted into CBA (H-2k) recipients. Mice received daily injections of everolimus (0.05 mg/kg) alone or combined with clopidogrel (1 mg/kg). Twenty-eight days after transplantation, ratio of the thickness of tracheal epithelium and lamina propria was measured as an indicator for chronic rejection. Additionally, graft oxygenation and graft perfusion were detected on postoperative days 4, 10 and 28. Quantitative reverse transcription polymerase chain reaction analysis was used for gene expression analysis.

resultsWhile syngeneic grafts showed a stable tissue pO2 and undisturbed microvascular perfusion, rejecting allografts had a drastic decline in both parameters as well as a flattened epithelium and an increased thickness of the lamina propria. Treatment with everolimus reduced allogeneic fibroproliferation, but had no protective effects on the microvasculature; polymerase chain reaction analysis indicated hypoxic stress and inflammation. Combining everolimus with clopidogrel improved microvascular integrity in the tracheal grafts, but had no synergistic effect in preventing obliterative bronchiolitis development.

conclusionsThese data demonstrate that the ability of everolimus to reduce the development of post-transplant obliterative bronchiolitis is not caused by microvascular protection and has no synergistic effects with clopidogrel in acute airway rejection.

Indexed as

TracheaAllograftsAnimalsBronchiolitis ObliteransClopidogrelEverolimusGraft RejectionLung TransplantationMiceMice, Inbred BALB CMice, Inbred C57BLMice, Inbred CBAMicrovesselsClopidogrelEverolimusBronchiolitis obliterans syndromeChronic lung allograft dysfunctionClopidogrelEverolimusMicrovascular integrityObliterative bronchiolitis

Identifiers

PMID33550369
PMCPMC8600037
OpenAlexW3127353412

What OpenQuestion holds

Textmetadata
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.