AI Article Synopsis

  • Advances in immunosuppressive protocols have improved short-term prevention and treatment of acute rejection in organ transplants, but long-term outcomes for solid organs have barely improved over the years.
  • Chronic allograft vasculopathy (CAV) is the leading cause of late organ failure in transplants, but its causes are still poorly understood, making effective treatments elusive.
  • The text presents a new mouse model for studying CAV through a non-suture cuff technique for aortic transplantation, aiming to facilitate better understanding and research into the development of CAV.

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Objective: To investigate the molecular mechanisms underlying the effects of arsenic trioxide (AsO) in combination with leflunomide on the hamster-to-rat heart xenotransplant.

Methods: Transplantation of LVG hamster hearts to Lewis rats was performed by anastomosis of vessels in the neck using end-to-end anastomosis with a non-suture cuff technique. Four groups of recipient rats (n=6 in each) were treated with normal saline (control), AsO [5 mg/(kg·day) intraperitoneally], leflunomide [5 mg/(kg·d) orally], or leflunomide [5 mg/(kg·d)+AsO [5 mg/(kg·d)] in combination.

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Combined treatment with vitamin D3 and antibody agents suppresses secondary heart transplant rejection in the early postoperative period.

Transpl Immunol

April 2020

Organ Transplantation institute, School of Medicine, Xiamen University, Xiamen, Fujian, China; Fujian Key Laboratory of Organ and Tissue Regeneration, Xiamen, Fujian, China; Medical College, Guangxi University, Nanning, Guangxi, China. Electronic address:

Background: Accelerated transplant rejection mediated by donor reactive memory T cells is another barrier to the induction of graft tolerance. The aim of this study was to investigate the immunosuppressing effects of vitamin D (1,25(OH)2D3), administered alone or in combination with a costimulatory blockade treatment, on rejection of secondary heart allografts in a mouse model.

Methods: Circular full-thickness skin grafts from BALB/c mice were cut and grafted onto the lumbar regions of C57BL/6 mice as allo-primed recipients.

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Murine Cervical Aortic Transplantation Model using a Modified Non-Suture Cuff Technique.

J Vis Exp

November 2019

Department of General, Visceral, and Transplant Surgery, Ludwig Maximilian University of Munich; Department of General, Visceral and Cancer Surgery, University Hospital of Cologne, University of Cologne;

Article Synopsis
  • Advances in immunosuppressive protocols have improved short-term prevention and treatment of acute rejection in organ transplants, but long-term outcomes for solid organs have barely improved over the years.
  • Chronic allograft vasculopathy (CAV) is the leading cause of late organ failure in transplants, but its causes are still poorly understood, making effective treatments elusive.
  • The text presents a new mouse model for studying CAV through a non-suture cuff technique for aortic transplantation, aiming to facilitate better understanding and research into the development of CAV.
View Article and Find Full Text PDF

Mouse Model for Pancreas Transplantation Using a Modified Cuff Technique.

J Vis Exp

December 2017

Center of Operative Medicine, Department of Visceral, Transplant and Thoracic Surgery, Medical University Innsbruck;

Mouse models have several advantages in transplantation research, including easy handling, a variety of genetically well-defined strains, and the availability of the widest range of molecular probes and reagents to perform in vivo as well as in vitro studies. Based on our experience with various murine transplantation models, we developed a heterotopic pancreas transplantation model in mice with the intent to analyze mechanisms underlying severe ischemia reperfusion injury-associated early graft damage. In contrast to previously described techniques using suture techniques, herein we describe a new procedure using a non-suture cuff technique.

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Orthotopic Hind Limb Transplantation in the Mouse.

J Vis Exp

February 2016

Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation (VCA) Laboratory, Johns Hopkins University School of Medicine;

In vivo animal model systems, and in particular mouse models, have evolved into powerful and versatile scientific tools indispensable to basic and translational research in the field of transplantation medicine. A vast array of reagents is available exclusively in this setting, including mono- and polyclonal antibodies for both diagnostic and interventional applications. In addition, a vast number of genotyped, inbred, transgenic, and knock out strains allow detailed investigation of the individual contributions of humoral and cellular components to the complex interplay of an immune response and make the mouse the gold standard for immunological research.

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