Evidence map›Paper›PMID 32859929›Full record

ArticleScientific reports2020

Non-invasive screening for subclinical liver graft injury in adults via donor-specific anti-HLA antibodies.

Anne Höfer, Danny Jonigk, Björn Hartleben, Murielle Verboom, Michael Hallensleben, Michael P Manns, Elmar Jaeckel, Richard Taubert

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 34 citations in OpenAlex.

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  12. Strategies for Liver Transplantation Tolerance.International journal of molecular sciences · 2021
    Review
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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

8 authors at 2 institutions in 1 country.

Anne HöferDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
Danny JonigkInstitute for Pathology, Hannover Medical School, Hannover, Germany.
Björn HartlebenInstitute for Pathology, Hannover Medical School, Hannover, Germany.
Murielle VerboomInstitute for Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.
Michael HallenslebenInstitute for Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.
Michael P MannsDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
Elmar JaeckelDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
Richard TaubertDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany. taubert.richard@mh-hannover.de.
Medizinische Hochschule Hannover · DEERN RARE-LIVER

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The majority of liver grafts exhibit abnormal histological findings late after transplantation, even when liver enzymes are normal. Such subclinical graft injuries were associated with rejection and fibrosis progression in recent studies. The identification of non-invasive biomarkers for subclinical graft injury might help to individualize immunosuppression. Therefore, graft injury was assessed in 133 liver biopsies with normal/near normal liver enzymes from a prospective liver biopsy program. Cytokeratin-18 cell death marker (M65) and donor specific anti-HLA antibodies (DSA) were measured as non-invasive markers in paired plasma samples in addition to routine parameters. M65 was associated with subclinical graft injury but this association was too weak for reasonable clinical application. DSA positivity was associated with more graft inflammation (OR = 5.4) and more fibrosis (OR = 4.2). Absence of DSA excluded fibrosis in 87-89%, while presence of DSA excluded histological criteria for immunosuppression minimization attempts in 92-97%. While CK18 cell death marker had no diagnostic value for the detection of subclinical liver graft injury, DSA testing can help to preselect patients for immunosuppression reduction in case of DSA negativity, while DSA positivity should prompt elastography or liver biopsy for the assessment of subclinical graft injury.

Indexed as

AdultAgedAllograftsBiomarkersBiopsyFemaleGraft RejectionGraft SurvivalHLA AntigensHumansImmunosuppression TherapyIsoantibodiesKeratin-18LiverLiver TransplantationMaleBiomarkersHLA AntigensIsoantibodiesKeratin-18M65 antigen, humanPeptide Fragments

Identifiers

PMID32859929
PMCPMC7455737
OpenAlexW3082562253

What OpenQuestion holds

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Registered trials

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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.