ABO-incompatible Pediatric Liver Transplantation With Antibody and B-cell Depletion-free Immunosuppressive Protoco in High Consanguinity Communities

被引:1
作者
Shagrani, Mohammad [1 ,2 ]
Kumar, Kishwer [1 ]
Baker, Alastair [3 ]
Al-Awwami, Moheeb [4 ]
Alhussaini, Hussa [5 ]
Almanea, Hadeel [5 ]
Alhumaidan, Hind [6 ]
Iorio, Raffaele [7 ]
Al-Khabbaz, Hana [8 ]
Burdelski, Martin [1 ]
Troisi, Roberto, I [9 ]
Broering, Dieter C. [1 ,2 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Pediat Gastroenterol, OTC, Organ Transplant Ctr, Riyadh, Saudi Arabia
[2] Al Faisal Univ, Med Coll, Riyadh, Saudi Arabia
[3] Kings Coll Hosp London, Paediat Liver Ctr, London, England
[4] King Faisal Specialist Hosp & Res Ctr, Dept Histocompatibil, Riyadh, Saudi Arabia
[5] King Faisal Specialist Hosp & Res Ctr, Dept Pathol & Lab Med, Riyadh, Saudi Arabia
[6] King Faisal Specialist Hosp & Res Ctr, Dept Blood Bank & Transfus Serv, Riyadh, Saudi Arabia
[7] Univ Federico II, Dept Translat Med Sci, Sect Pediat, Naples, Italy
[8] Riyadh Elm Univ, Dept Pharm, Riyadh, Saudi Arabia
[9] Federico II Univ Hosp, Dept Clin Med & Surg, Div HPB Minimally Invas & Robot Surg, Renal Transplantat Serv, Naples, Italy
来源
TRANSPLANTATION DIRECT | 2022年 / 8卷 / 12期
关键词
RITUXIMAB; COMPLEMENT; MANAGEMENT; SINGLE; IMMUNOHISTOCHEMISTRY; CHILDREN; AGE;
D O I
10.1097/TXD.0000000000001353
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. The success of orthotopic liver transplantation as a life-saving treatment has led to new indications and a greater competition for organ grafts. Pediatric patients with acute liver-related crises can benefit from orthotopic liver transplantation, but organ availability in the limited time can be a major obstacle. Crossing ABO blood group barriers could increase the organs available to such patients Methods. From November 2010 to June 2015, 176 children aged 0.2-to18 y were transplanted in the King Faisal Specialist Hospital and Research Center. Out of those, 19 children were transplanted across blood group barriers (ABO incompatible). The underlying diseases were biliary atresia (n = 6); progressive familial intrahepatic cholestasis type 2 (n = 4); Crigler-Najjar syndrome (n = 3); hepatoblastoma (n = 2); and urea cycle disorder, Caroli disease, cryptogenic cirrhosis, and neonatal sclerosing cholangitis (n = 1 each). Immunosuppression consisted of basiliximab, mycophenolate, tacrolimus, and steroids. Pretransplant prophylactic plasmapheresis, high-dose immunoglobulins, and rituximab were not administered. Results. The grafts were from living donors (n = 17) and deceased donors (n = 2). Living donor morbidity was nil. The recipient median age was 21 mo (5-70 mo). After a median follow-up of 44 mo, 2 recipients (10%) died because of sepsis, 1 because of uncontrolled acute myeloid leukemia. The overall rejection rate was 7%, and no grafts were lost because of antibody-mediated rejection (AMR). HLA matching was 3.8 of 6 (A, B, DR), and there were 2 patients presented with acute cellular rejection, 1 patient with AMR, and 1 patient with biliary strictures. Conclusions. ABO incompatible liver transplantation is a feasible and life-saving option even with antibody and B-cell depletion-free protocol without increasing the risks for AMR. We speculate that this excellent result is most likely because of presence of relatively low titer ABO isoagglutinins and the high HLA match compatibility caused by habit of longstanding interfamilial marriages as typical of Saudi Arabia.
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