Pediatric liver transplantation: Personal perspectives on historical achievements and future challenges

被引:28
|
作者
Otte, Jean-Bernard [1 ]
机构
[1] Catholic Univ Louvain, Dept Pediat Surg & Liver Transplantat, Clin St Luc, 273 Ave Chapelle, B-1950 Brussels, Belgium
关键词
POSTTRANSPLANT LYMPHOPROLIFERATIVE DISEASE; SOLID-ORGAN TRANSPLANTATION; BONE-MARROW AUGMENTATION; ONE DONOR LIVER; LIVING-DONOR; HEPATIC TRANSPLANTATION; INTERNATIONAL-SOCIETY; AUTOIMMUNE HEPATITIS; STEROID WITHDRAWAL; ALLOGRAFT FIBROSIS;
D O I
10.1002/lt.24470
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
This review presents the author's personal perspective and contributions to the first steps, the development, the current status, and the remaining issues of pediatric liver transplantation (LT). Innumerable children around the world who have undergone LT have reached adulthood. The techniques have reached maturity. As shown by my own group's experience, grafts donated by living donors might provide the best short-term and longterm results. Debate persists about the optimal immunosuppression (IS), although the place of tacrolimus remains unchallenged. Tolerance induction protocols aiming to induce microchimerism have been tried in clinical transplantation without convincing results. Withdrawal of maintenance IS is possible in some children who underwent liver transplantation who have excellent clinical status and normal liver function tests but is not without risk of rejection and subsequent worsening of histology. The current trend favored by the Brussels' group is to minimize IS as soon after transplant as possible, aiming to obtain a state of prope or almost tolerance. Liver grafts are threatened in the long term by increasing hepatitis-related fibrosis, resulting most likely from immunological assault. Nowadays, the focus is on the longterm survival, quality of life (growth, academic performance, employment, self-fulfillment, fertility, raising a family, etc.), induction of tolerance, prevention of risks bound to decades of IS (nephrotoxicity and neurotoxicity, cardiovascular risk, de novo malignancies, etc.), and prevention of graft fibrosis. All these issues are fertile fields for younger scientists. Liver Transplantation 22 1284-1294 2016 AASLD
引用
收藏
页码:1284 / 1294
页数:11
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