Recipient risk factors for acute cellular rejection after orthotopic liver transplant - a single-center,

David Choi1,2, Mengyuan Liu1, Dharani Guttikonda3

  • 1Division of Gastroenterology and Hepatology, University of Illinois at Chicago, Chicago, IL, USA.

Insights

The Model for End-Stage Liver Disease (MELD) score era has changed acute cellular rejection (ACR) characteristics after liver transplants. Higher MELD scores are linked to altered ACR timing and severity, impacting immunosuppression strategies.

Area of Science:

  • Hepatology
  • Transplant Immunology
  • Nephrology

Background:

  • The Model for End-Stage Liver Disease (MELD) score implementation changed liver allocation, leading to sicker patients undergoing orthotopic liver transplant (OLT).
  • This shift raises questions about potential changes in the risk factors and severity of acute cellular rejection (ACR).

Purpose of the Study:

  • To investigate the characteristics of ACR in adult OLT recipients transplanted during the MELD score era.
  • To identify specific risk factors associated with ACR development in patients receiving a steroid-sparing immunosuppression regimen.

Main Methods:

  • A retrospective analysis of 174 adult OLT patients transplanted between 2008 and 2013 at a single tertiary care center.
  • Collection of recipient demographics, preoperative clinical data, and laboratory results.
  • Univariate and multivariate regression analyses to determine significant predictors of ACR.

Main Results:

  • The median MELD score at transplantation was 29.5.
  • The average time to ACR diagnosis was 283.9 days, with most episodes being mild to moderate.
  • Serum creatinine levels, primary sclerosing cholangitis as the liver disease etiology, and tacrolimus use were identified as significant predictors of ACR (P < 0.05).

Conclusions:

  • The study confirms a shift in the timing and severity of ACR in the MELD score era.
  • Recipient characteristics, including serum creatinine and specific disease etiologies, are crucial factors influencing ACR risk.
  • These findings suggest that individualized immunosuppression management is necessary to address altered ACR profiles in the current transplant landscape.

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