Organ Transplantation Center, National Center for Child Health and Development, Tokyo, Japan.
Division of Transplant Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, USA.
J Hepatol. 2023 Jun;78(6):1147-1156. doi: 10.1016/j.jhep.2022.10.013.
Living donor liver transplantation (LDLT) is recognised as an alternative treatment modality to reduce waiting list mortality and expand the donor pool. Over recent decades, there have been an increasing number of reports on the use of LT and specifically LDLT for familial hereditary liver diseases. There are marginal indications and contraindications that should be considered for a living donor in paediatric parental LDLT. No mortality or morbidity related to recurrence of metabolic diseases has been observed with heterozygous donors, except for certain relevant cases, such as ornithine transcarbamylase deficiency, protein C deficiency, hypercholesterolemia, protoporphyria, and Alagille syndrome, while donor human leukocyte antigen homozygosity also poses a risk. It is not always essential to perform preoperative genetic assays for possible heterozygous carriers; however, genetic and enzymatic assays must hereafter be included in the parental donor selection criteria in the aforementioned circumstances.
活体肝移植(LDLT)被认为是一种替代治疗方法,可以降低等待名单死亡率并扩大供体池。在过去几十年中,越来越多的关于 LT 和特别是 LDLT 在家族遗传性肝脏疾病中的应用的报告。对于儿科父母 LDLT 中的活体供体,存在一些边缘适应症和禁忌症需要考虑。除了某些相关病例,如鸟氨酸转氨甲酰酶缺乏症、蛋白 C 缺乏症、高胆固醇血症、原卟啉症和 Alagille 综合征外,杂合子供体没有与代谢疾病复发相关的死亡率或发病率,而供体人类白细胞抗原纯合子也存在风险。对于可能的杂合子携带者,并非总是需要进行术前遗传检测;然而,在上述情况下,遗传和酶检测必须包含在父母供体选择标准中。