Literature DB >> 27037650

The Leuven Immunomodulatory Protocol Promotes T-Regulatory Cells and Substantially Prolongs Survival After First Intestinal Transplantation.

L J Ceulemans1, F Braza2, D Monbaliu1, I Jochmans1, G De Hertogh3, J Du Plessis4, M-P Emonds5,6, H Kitade6, M Kawai6, Y Li7, X Zhao7, T Koshiba6,7, B Sprangers6, S Brouard2, M Waer6, J Pirenne1.   

Abstract

Intestinal transplantation (ITx) remains challenged by frequent/severe rejections and immunosuppression-related complications (infections/malignancies/drug toxicity). We developed the Leuven Immunomodulatory Protocol (LIP) in the lab and translated it to the clinics. LIP consists of experimentally proven maneuvers, destined to promote T-regulatory (Tregs)-dependent graft-protective mechanisms: donor-specific blood transfusion (DSBT); avoiding high-dose steroids/calcineurin-inhibitors; and minimizing reperfusion injury and endotoxin translocation. LIP was tested in 13 consecutive ITx from deceased donors (2000-2014) (observational cohort study). Recipient age was 37 years (2.8-57 years). Five-year graft/patient survival was 92%. One patient died at 9 months due to aspergillosis, another at 12 years due to nonsteroidal anti-inflammatory drug-induced enteropathy. Early acute rejection (AR) developed in two (15%); late AR in three (23%); all were reversible. No chronic rejection (CR) occurred. No malignancies developed and estimated glomerular filtration rate remained stable post-Tx. At last follow-up (3.5 years [0.5-12.5 years]), no donor-specific antibodies were detected and 11 survivors were total parenteral nutrition free with a Karnofsky score >90% in 8 recipients (follow-up >1 years). A high frequency of circulating CD4+ CD45RA- Foxp3hi memory Tregs was found (1.8% [1.39-2.21]), comparable to tolerant kidney transplant (KTx) recipients and superior to stable immunosuppression (IS)-KTx, KTx with CR, and healthy volunteers. In this ITx cohort we show that DSBT in a low-inflammatory/pro-regulatory environment activates Tregs at levels similar to tolerant-KTx, without causing sensitization. LIP limits rejection under reduced IS and thereby prolongs long-term survival to an extent not previously attained after ITx. © Copyright 2016 The American Society of Transplantation and the American Society of Transplant Surgeons.

Entities:  

Keywords:  T cell biology; clinical research/practice; immune regulation; intestinal disease; intestine/multivisceral transplantation; tolerance: clinical; translational research/science

Mesh:

Year:  2016        PMID: 27037650     DOI: 10.1111/ajt.13815

Source DB:  PubMed          Journal:  Am J Transplant        ISSN: 1600-6135            Impact factor:   8.086


  5 in total

Review 1.  Chronic Rejection After Intestinal Transplant: Where Are We in Order to Avert It?

Authors:  Augusto Lauro; Mihai Oltean; Ignazio R Marino
Journal:  Dig Dis Sci       Date:  2018-01-11       Impact factor: 3.199

Review 2.  Update on immunosuppressive strategies in intestinal transplantation.

Authors:  Jonathan Merola; Abrar Shamim; Joshua Weiner
Journal:  Curr Opin Organ Transplant       Date:  2022-04-01       Impact factor: 2.640

Review 3.  Innovations in Immunosuppression for Intestinal Transplantation.

Authors:  Harween Dogra; Jonathan Hind
Journal:  Front Nutr       Date:  2022-06-15

4.  Long-Term Signs of T Cell and Myeloid Cell Activation After Intestinal Transplantation With Cellular Rejections Contributing to Further Increase of CD16+ Cell Subsets.

Authors:  Nadja Stobutzki; Stephan Schlickeiser; Mathias Streitz; Katarina Stanko; Kim-Long Truong; Levent Akyuez; Katrin Vogt; Christine Appelt; Andreas Pascher; Olga Blau; Undine A Gerlach; Birgit Sawitzki
Journal:  Front Immunol       Date:  2019-05-07       Impact factor: 7.561

5.  Robotic-Assisted Live Donor Ileal Segmentectomy for Intestinal Transplantation.

Authors:  Guosheng Wu; Qianjing Li; Qingchuan Zhao; Weizhong Wang; Hai Shi; Mian Wang; Jianyong Zheng; Mengbing Li; Daiming Fan
Journal:  Transplant Direct       Date:  2017-09-21
  5 in total

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