Evidence map›Paper›PMID 40362208›Full record

ReviewInternational journal of molecular sciences2025

Tolerogenic Therapies in Cardiac Transplantation.

Laurenz Wolner, Johan William-Olsson, Bruno K Podesser, Andreas Zuckermann, Nina Pilat

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Gene-edited pig cardiac xenotransplantation as a bridge to allotransplantation in infants: Progress in a pig-to-baboon model.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Article
  2. Review
  3. Review
  4. 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

5 authors.

Laurenz WolnerCenter for Biomedical Research and Translational Surgery, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0009-0005-4266-9321
Johan William-OlssonCenter for Biomedical Research and Translational Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Bruno K PodesserCenter for Biomedical Research and Translational Surgery, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-4641-7202
Andreas ZuckermannDepartment of Cardiac and Thoracic Aortic Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Nina PilatCenter for Biomedical Research and Translational Surgery, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0003-4071-9397

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heart transplantation remains the gold-standard treatment for end-stage heart failure, yet long-term graft survival is hindered by chronic rejection and the morbidity and mortality caused by lifelong immunosuppression. While advances in medical and device-based therapies have reduced the overall need for transplantation, patients who ultimately require a transplant often present with more advanced disease and comorbidities. Recent advances in tolerance-inducing strategies offer promising avenues to improve allograft acceptance, while minimizing immunosuppressive toxicity. This review explores novel approaches aiming to achieve long-term immunological tolerance, including co-stimulation blockade, mixed chimerism, regulatory T-cell (Treg) therapies, thymic transplantation, and double-organ transplantation. These strategies seek to promote donor-specific unresponsiveness and mitigate chronic rejection. Additionally, expanding the donor pool remains a critical challenge in addressing organ shortages. Innovations such as ABO-incompatible heart transplantation are revolutionizing the field by increasing donor availability and accessibility. In this article, we discuss the mechanistic basis, clinical advancements, and challenges of these approaches, highlighting their potential to transform the future of heart transplantation with emphasis on clinical translation.

Indexed as

Graft RejectionHeart TransplantationImmune ToleranceTransplantation ToleranceAnimalsGraft SurvivalHumansImmunosuppression TherapyImmunosuppressive AgentsT-Lymphocytes, RegulatoryImmunosuppressive Agentsheart transplantationimmune tolerancetolerogenic therapies

Identifiers

PMID40362208
PMCPMC12072115

What OpenQuestion holds

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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.