Evidence map›Paper›PMID 41595984›Full record

ArticleBioengineering (Basel, Switzerland)2025

Antibody and Cellular Immune Responses in Old α1,3-Galactosyltransferase-Knockout Mice Implanted with Bioprosthetic Heart Valve Tissues.

Kelly Casós, Roger Llatjós, Arnau Blasco-Lucas, Sebastián G Kuguel, Fabrizio Sbraga, Cesare Galli, Vered Padler-Karavani, Thierry Le Tourneau, Marta Vadori, Jean-Christian Roussel and 6 more

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2025. 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
–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

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

16 authors.

Kelly CasósInfectious Diseases and Transplantation Division, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, 08908 Barcelona, Spain.
Roger LlatjósPathology Department, Bellvitge University Hospital, L'Hospitalet de Llobregat, 08907 Barcelona, Spain.ORCID 0000-0002-0566-9577
Arnau Blasco-LucasCardiac Surgery Department, Bellvitge University Hospital, L'Hospitalet de Llobregat, 08907 Barcelona, Spain.ORCID 0000-0002-2796-7428
Sebastián G KuguelInfectious Diseases and Transplantation Division, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, 08908 Barcelona, Spain.ORCID 0000-0001-7213-6503
Fabrizio SbragaCardiac Surgery Department, Bellvitge University Hospital, L'Hospitalet de Llobregat, 08907 Barcelona, Spain.ORCID 0000-0003-1249-4119
Cesare GalliAvantea, Laboratory of Reproductive Technologies, Via Porcellasco 7/F, 26100 Cremona, Italy.ORCID 0000-0002-9529-6136
Vered Padler-KaravaniDepartment of Cell Research and Immunology, The Shmunis School of Biomedicine and Cancer Research, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.ORCID 0000-0002-4761-3571
Thierry Le TourneauInstitut du Thorax, INSERM UMR1087, Nantes University Hospital, 8 Quai Moncousu, 44007 Nantes, France.ORCID 0000-0002-0110-9054
Marta VadoriTransplantation Immunology Unit, Padua University Hospital, 35128 Padova, Italy.ORCID 0000-0002-9763-2383
Jean-Christian RousselInstitut du Thorax, INSERM UMR1087, Nantes University Hospital, 8 Quai Moncousu, 44007 Nantes, France.ORCID 0000-0003-3928-6977
Tomaso BottioDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova Medical School, 35122 Padova, Italy.ORCID 0000-0001-7299-2983
Emanuele CozziTransplantation Immunology Unit, Padua University Hospital, 35128 Padova, Italy.ORCID 0000-0001-7855-5055
Jean-Paul SoulillouInstitut de Transplantation-Urologie-Néphrologie, INSERM Unité Mixte de Recherche 1064, Nantes University Hospital, 44093 Nantes, France.ORCID 0000-0001-7468-5135
Manuel GaliñanesDepartment of Cardiac Surgery and Reparative Therapy of the Heart, Vall d'Hebron Research Institute (VHIR), University Hospital Vall d'Hebron, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.ORCID 0000-0002-0888-976X
Rafael MáñezInfectious Diseases and Transplantation Division, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, 08908 Barcelona, Spain.ORCID 0000-0002-0884-5564
Cristina CostaInfectious Diseases and Transplantation Division, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, 08908 Barcelona, Spain.ORCID 0000-0002-1837-4268

Funding

European Union Seventh Framework Programme FP7/2007 - 2013: 603049Ministerio de Economía y Competitividad-ISCiii PI15/00181PERIS, Department of Health of Generalitat de Catalunya SLT002/16/00445
6 · The paper itself

Abstract

Structural valve deterioration (SVD) remains a key limitation in bioprosthetic heart valve (BHV) usage influenced by patient age. A deeper understanding of SVD pathogenesis, particularly of the immune-mediated processes altering current BHV materials, is therefore critical. To this end, commercially available BHV tissues of bovine, porcine, and equine origin were investigated following subcutaneous implantation into α1,3-galactosyltransferase-knockout (Gal KO) mice. We compared the immune responses between adult and aged animals via histological assessments of explants and measurement of serum anti-galactose α1,3-galactose (Gal) and anti-non-Gal antibodies at 2 months post-implantation. In contrast to adult mice, old Gal KO mice did not show increased levels of serum anti-Gal or -non-Gal antibodies after receiving specific BHV tissue (i.e., Freedom-Solo). Instead, a significant decrease in serum anti-Gal IgM was found in old recipients of Freedom-Solo. Furthermore, the overall cellular immune response was attenuated in explants from old mice compared with adults (i.e., ATS 3f and Crown). Nevertheless, the Freedom-Solo (bovine) and the Hancock-II (porcine) tissues still elicited strong cellular immune infiltration in the old cohorts. Therefore, the Gal KO mouse model offers a valuable platform to investigate age-related differences regarding cellular and humoral immune responses to various BHV tissues, contributing to our understanding of SVD.

Indexed as

aginganti-Gal antibodiesbioprosthetic heart valvescellular immune responsestructural valve deteriorationα1,3-galactosyltransferase-knockout mice

Identifiers

PMID41595984
PMCPMC12838042

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.