Long-term outcomes following ABO-incompatible living donor liver transplantation for acute liver failure: a single-center experience of over 20 years

Surg Today. 2023 Oct;53(10):1160-1172. doi: 10.1007/s00595-023-02678-w. Epub 2023 Jun 5.

Abstract

Purpose: Acute liver failure is a life-threatening condition for which ABO-incompatible living donor liver transplantation (ABOi-LDLT) is sometimes the only life-saving treatment option. We reviewed a single-center experience of adult ABOi-LDLT treatment for acute liver failure (ALF).

Methods: Preoperative treatment, immune indices (B cell marker, anti-donor blood-type antibody), and postoperative outcomes were compared between ALF and non-ALF groups.

Results: There were 5 and 33 patients in the ALF and non-ALF groups, respectively. The ALF group received higher doses of steroids, underwent more rounds of plasma exchange (PE), and underwent transplantation for ALF with a shorter interval following preoperative rituximab (RTx) administration (median: 2 vs 13 days; P < 0.05) than the non-ALF group. Preoperatively, CD19-positive lymphocytes in the peripheral blood were sufficiently depleted in all of the non-ALF group patients, whereas they were poorly depleted in the ALF group. Postoperatively, neither group suffered anti-donor blood-type antibody titer rebound or antibody-mediated rejection. The ALF group had a comparable 5-year survival rate to the non-ALF group (80.0% vs 77.9%).

Conclusions: Despite the delayed preoperative administration of RTx, the ALF group showed an uneventful immunological response and acceptable long-term survival rate. Thus, ABOi-LDLT seems a viable treatment option for ALF.

Keywords: ABO incompatible; Acute liver failure; Living donor liver transplantation; Rituximab; Steroids.

MeSH terms

  • ABO Blood-Group System
  • Adult
  • Blood Group Incompatibility
  • Graft Rejection
  • Humans
  • Liver Failure, Acute* / drug therapy
  • Liver Failure, Acute* / surgery
  • Liver Transplantation*
  • Living Donors
  • Rituximab / therapeutic use

Substances

  • ABO Blood-Group System
  • Rituximab