Evidence map›Paper›PMID 42120756›Full record

ArticleCommunications medicine2026

Exploring donor-derived cell-free DNA as a rejection biomarker during uterus transplant follow up.

Eva González-Roca, Mariona Rius, María José Ramírez-Bajo, Aina Montalbán-Casafont, Elisenda Bañón-Maneus, Natalia Hierro-García, Mireia Musquera, Adela Saco, Antonio Alcaraz, Mercè Brunet and 4 more

Abstract read
In one paragraph

Article in Communications medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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.

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

14 authors.

Eva González-Roca *Molecular Biology CORE Lab, CDB, Hospital Clínic de Barcelona (HCB), Barcelona, Spain.ORCID http://orcid.org/0000-0002-1126-0321
Mariona Rius *Department of Gynecology, Institut Clínic de Ginecologia, Obstetrícia, i Neonatologia, HCB, Barcelona, Spain.
María José Ramírez-BajoLaboratori Experimental de Nefrologia i Trasplantament (LENIT), Fundació per a la Recerca Biomèdica - Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Aina Montalbán-CasafontMolecular Biology CORE Lab, CDB, Hospital Clínic de Barcelona (HCB), Barcelona, Spain.ORCID http://orcid.org/0000-0002-1842-9441
Elisenda Bañón-ManeusLaboratori Experimental de Nefrologia i Trasplantament (LENIT), Fundació per a la Recerca Biomèdica - Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Natalia Hierro-GarcíaLaboratori Experimental de Nefrologia i Trasplantament (LENIT), Fundació per a la Recerca Biomèdica - Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Mireia MusqueraDepartment of Urology, HCB, Barcelona, Spain.
Adela SacoPathology Department, CDB, HCB, Barcelona, Spain.
Antonio AlcarazDepartment of Urology, HCB, Barcelona, Spain.
Mercè BrunetFarmacologia i Toxicologia, Servei de Bioquímica i Genètica Molecular, Centre de Diagnòstic Biomèdic.Hospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain.
Eduard PalouDepartment of Immunology, HCB, Barcelona, Spain.ORCID http://orcid.org/0000-0003-1544-1485
Fritz DiekmannLaboratori Experimental de Nefrologia i Trasplantament (LENIT), Fundació per a la Recerca Biomèdica - Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Francisco Carmona *Department of Gynecology, Institut Clínic de Ginecologia, Obstetrícia, i Neonatologia, HCB, Barcelona, Spain. Fcarmona@clinic.cat.ORCID http://orcid.org/0000-0002-0172-1761
Joan Anton Puig-Butillé *Molecular Biology CORE Lab, CDB, Hospital Clínic de Barcelona (HCB), Barcelona, Spain.ORCID http://orcid.org/0000-0003-4345-9631

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUterus transplantation (UTx) is a treatment option for women with absolute uterine factor infertility who wish to become pregnant and have a healthy live birth. Tissue biopsy is the gold standard for diagnosing allograft rejection. Circulating donor-derived cell-free DNA (dd-cfDNA) has recently emerged as a non-invasive biomarker with strong predictive value for rejection in solid organ transplants.

methodsdd-cfDNA quantification by next-generation sequencing (NGS) was evaluated in two UTx patients from transplantation to childbirth. The results were compared with cervical biopsies. Additionally, capillary electrophoresis was used to characterize cfDNA fragmentation pattern.

resultsdd-cfDNA levels significantly increase during biopsy-proven rejection episodes (0.39% vs 0.17% in patient 1 and 0.34% vs 0.26% in patient 2). Additionally, cfDNA fragment analysis shows an elevation of high molecular weight cfDNA fragments during rejection.

conclusionsThese findings support dd-cfDNA as a promising non-invasive tool for monitoring UTx rejection. Future studies should focus on characterizing dd-cfDNA kinetics and cfDNA fragmentomics in larger cohorts to optimize rejection detection and improve patient outcomes.

Identifiers

PMID42120756
PMCPMC13389477

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