Tailored strategies for emergency ABO-incompatible living donor liver transplantation: a series of three cases

ABO-incompatible (ABOi) living donor liver transplantation (LDLT) carries a substantial risk of antibody-mediated rejection (AMR) in both the short and long term. However, when no ABO-compatible donor is available, ABOi LDLT can be a viable option for patients with liver failure requiring emergency transplantation. To prevent AMR, various strategies have been implemented. However, typically, a pretransplant preparation period of at least 2 to 3 weeks is required to reduce the CD19+ or CD20+ cell count and antibody levels to an acceptable threshold (1:64). In emergency ABOi cases, due to time constraints, the desensitization protocol must be modified in accordance with the patient's needs. We present a series of three cases involving emergency ABOi LDLT: one of primary graft nonfunction and two of acute-on-chronic liver failure. The goal was to achieve both short- and long-term rejection-free outcomes. Each case required different protocols based on the patient's antibody titer, clinical condition, and intraoperative findings, and postoperative immunosuppression regimens were also individualized according to each patient's clinical condition. This case series demonstrates the safety and feasibility of emergency ABOi LDLT with modifications to the desensitization protocol. However, further research into emergency ABOi transplantation is necessary to establish recommendations for managing such patients.

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Publication Details

Journal
Clinical Transplantation and Research
Published
2025-02-18
DOI
https://doi.org/10.4285/ctr.24.0061
Citations
1
Primary Topic
Liver Disease and Transplantation
Type
article
Field-Weighted Citation Impact
1.32
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article

Tailored strategies for emergency ABO-incompatible living donor liver transplantation: a series of three cases

Nalini Kanta Ghosh, Vivek Vij, Kausar Makki, Piyush Srivastava et al.
1 citations
Clinical Transplantation and Research
Liver Disease and Transplantation
1.32
article

Tailored strategies for emergency ABO-incompatible living donor liver transplantation: a series of three cases

Nalini Kanta Ghosh, Vivek Vij, Kausar Makki, Piyush Srivastava, Yogesh Yadav, Anil K. Agarwal, Tathagata Karan
article en
1 citations

Abstract

ABO-incompatible (ABOi) living donor liver transplantation (LDLT) carries a substantial risk of antibody-mediated rejection (AMR) in both the short and long term. However, when no ABO-compatible donor is available, ABOi LDLT can be a viable option for patients with liver failure requiring emergency transplantation. To prevent AMR, various strategies have been implemented. However, typically, a pretransplant preparation period of at least 2 to 3 weeks is required to reduce the CD19+ or CD20+ cell count and antibody levels to an acceptable threshold (1:64). In emergency ABOi cases, due to time constraints, the desensitization protocol must be modified in accordance with the patient's needs. We present a series of three cases involving emergency ABOi LDLT: one of primary graft nonfunction and two of acute-on-chronic liver failure. The goal was to achieve both short- and long-term rejection-free outcomes. Each case required different protocols based on the patient's antibody titer, clinical condition, and intraoperative findings, and postoperative immunosuppression regimens were also individualized according to each patient's clinical condition. This case series demonstrates the safety and feasibility of emergency ABOi LDLT with modifications to the desensitization protocol. However, further research into emergency ABOi transplantation is necessary to establish recommendations for managing such patients.

Clinical Transplantation and ResearchVol. 39(2)
Fortis Healthcare (IN), Fortis Hospital (IN)
Zero hunger
Openalex Percentile: Top 24%
Liver Disease and Transplantation
1.32
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Tailored strategies for emergency ABO-incompatible living donor liver transplantation: a series of three cases — Nalini Kanta Ghosh, Vivek Vij, et al. · Clinical Transplantation and Research (2025) | TGRS Research Map | TGRS