Shimata Keita, Sakamoto Rieko, Anan Tadashi, Uchida Koushi, Honda Masaki, Kouroki Masahiko, Urabe Tomonari, Hayashida Shintaro, Yamamoto Hidekazu, Sugawara Yasuhiko, Inomata Yukihiro
Department of Transplantation and Pediatric Surgery, Kumamoto University Hospital, Kumamoto, Japan.
Department of Pediatrics, Kumamoto University Hospital, Kumamoto, Japan.
Pediatr Transplant. 2017 Nov;21(7). doi: 10.1111/petr.13039. Epub 2017 Aug 19.
Acute GVHD is a rare complication after liver transplantation that has a high mortality rate. We experienced an infant case complicated with acute GVHD. An 8-month-old infant with biliary atresia underwent LDLT with a graft obtained from his mother. Their HLAs showed a donor-dominant one-way match, not at HLA-DR but at HLA-A, HLA-B, and HLA-C (recipient; A 31/33, B 51/54, C 1/14, DR 9/11, donor; A 31/-, B 51/-, C 14/-, DR 8/11). The patient exhibited a high fever, skin rash, and diarrhea, and was diagnosed with acute GVHD based on the blood chimerism test. Despite immunosuppression treatment with prednisolone and tacrolimus, plasma exchange, blood transfusion including cord blood transplantation, and antibiotics, the child died on postoperative day 126. Donor-dominant one-way matching at HLA class 1 can be a high-risk factor for acute GVHD despite HLA class 2 mismatching.
急性移植物抗宿主病是肝移植后一种罕见的并发症,死亡率很高。我们遇到了一例合并急性移植物抗宿主病的婴儿病例。一名8个月大的胆道闭锁婴儿接受了活体肝移植,供肝来自其母亲。他们的人类白细胞抗原显示为供体主导的单向匹配,不是在人类白细胞抗原-DR位点,而是在人类白细胞抗原-A、人类白细胞抗原-B和人类白细胞抗原-C位点(受者;A 31/33,B 51/54,C 1/14,DR 9/11,供者;A 31/ -,B 51/ -,C 14/ -,DR 8/11)。该患者出现高热、皮疹和腹泻,基于血液嵌合体检测被诊断为急性移植物抗宿主病。尽管使用泼尼松龙和他克莫司进行免疫抑制治疗、进行了血浆置换、包括脐血移植在内的输血以及使用了抗生素,但患儿仍在术后第126天死亡。尽管人类白细胞抗原2类位点不匹配,但人类白细胞抗原1类位点的供体主导单向匹配可能是急性移植物抗宿主病的一个高危因素。