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

Am J Transplant. 2016 Oct;16(10):2973-2985. doi: 10.1111/ajt.13815. Epub 2016 May 12.

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.

Trial registration: ClinicalTrials.gov NCT02314949.

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

Publication types

  • Clinical Trial
  • Observational Study

MeSH terms

  • Adolescent
  • Adult
  • Blood Transfusion
  • Child
  • Child, Preschool
  • Cohort Studies
  • Female
  • Follow-Up Studies
  • Graft Rejection / immunology
  • Graft Rejection / mortality*
  • Graft Rejection / prevention & control
  • Graft Survival / immunology*
  • Humans
  • Immune Tolerance / immunology*
  • Immunosuppression Therapy
  • Intestinal Diseases / surgery*
  • Intestines / transplantation*
  • Male
  • Middle Aged
  • Prognosis
  • Risk Factors
  • Survival Rate
  • T-Lymphocytes, Regulatory / immunology*
  • Tissue Donors
  • Transplantation, Homologous
  • Young Adult

Associated data

  • ClinicalTrials.gov/NCT02314949