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Objectives: Pulmonary allografts are commonly used for right ventricular outflow tract reconstruction. Cryopreserved allografts may develop degeneration and stenosis over time due to immune-related issues. Fresh decellularized aortic and pulmonary allografts have shown favourable early outcomes. We used a sheep model to evaluate the safety of a novel decellularization protocol combined with cryopreservation applied on pulmonary allografts, aiming to improve availability and reduce cost.
Methods: Pulmonary valve replacement was performed in juvenile female sheep using cryopreserved pulmonary allograft (n = 9) and decellularized cryopreserved pulmonary allograft (n = 10). Haemodynamics were investigated by transthoracic echocardiography and magnetic resonance imaging. Allografts were explanted at 6 months for macroscopic comparison, calcium quantification using X-ray imaging and spectrometry, histological and immunohistochemical characterization.
Results: There was one operative death in each group. There were no significant haemodynamic differences between groups regarding peak gradient (P = 0.14) or degree of regurgitation (P = 0.67) at 6 months. Calcium content of macroscopically non-calcified tissue was statistically similar (P = 0.16). Overall, decellularized tissues were smooth and supple. Cryopreserved allografts developed pannus formation and pronounced subvalvular calcifications. Some grafts in both groups showed luminal fibrin thrombi, calcified in cryopreserved grafts. Histologically, cryopreserved tissues contained more inflammatory cells. Decellularized grafts had lower cell presence, acellular inner media and valve with occasional fibrin covering. No true endothelium was seen in the stained samples except at the anastomoses.
Conclusions: Haemodynamically, both cryopreserved allografts and allografts decellularized according to the newly-developed protocol produced equivalent and favourable outcomes. Decellularized allografts showed less inflammation, less pannus formation and less calcification on X-ray imaging.
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http://dx.doi.org/10.1093/icvts/ivaf131 | DOI Listing |
Eur J Immunol
September 2025
CHU Nantes, Nantes Université, INSERM, Centre de Recherche Translationnelle En Transplantation et Immunologie (CR2TI), Nantes, France.
In the field of lung transplantation (LTx), the survival of lung transplant recipients (LTRs) is limited by events such as primary graft dysfunction (PGD), infections, and acute rejection (AR), which promote the development of chronic lung allograft dysfunction (CLAD). Extracellular vesicles (EVs), including exosomes and microvesicles, have emerged as key players in LTx because of their roles in immune regulation, inflammation, and antigen presentation. EVs carry immunologically active molecules such as MHC class I/II proteins, cytokines, and lung self-antigens (SAgs), suggesting their involvement in infections and both AR and CLAD.
View Article and Find Full Text PDFEur J Intern Med
September 2025
University Hospitals Leuven, Department of Respiratory Diseases, Leuven, Belgium; KU Leuven, Department CHROMETA, BREATHE, Leuven, Belgium. Electronic address:
Transpl Immunol
September 2025
Department of Pediatrics, School of Medicine, Alborz University of Medical Sciences, Karaj, Iran.
Background And Aim: Lung transplantation (LTx) is increasingly performed worldwide, yet post-transplant survival remains lower than for other solid organs. Diabetes mellitus (DM) is common among LTx recipients and impacts outcomes. This systematic review evaluates the effects of DM on LTx outcomes and the influence of diabetes onset timing on survival.
View Article and Find Full Text PDFAm J Case Rep
September 2025
Department of Infectious Disease, University of California, Irvine, CA, USA.
BACKGROUND Adenoviruses are double-stranded DNA viruses capable of causing a spectrum of diseases from mild respiratory infections to severe systemic illnesses. Disseminated adenovirus is evidenced by gastrointestinal, pulmonary, genitourinary, neurologic and even cardiac involvement. In immunocompromised individuals, adenovirus infections can become severe and are often associated with significant morbidity and mortality.
View Article and Find Full Text PDFRes Sq
August 2025
Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School; Boston, MA, USA.
We previously showed that infiltrating cytotoxic immune cells are reprogrammed to regulatory-like/exhausted cells within accepted kidney allografts through a 'defensive tolerance' mechanism. We observed a regulatory B cell (Breg) signature within the accepted kidney. Here we show that despite a Breg phenotype, neither B cell depletion nor the use of μMT recipients which lack B cells, resulted in kidney allograft rejection.
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