van der Windt Dirk J, Echeverri Gabriel J, Ijzermans Jan N M, Cooper David K C
Division of Immunogenetics, Department of Pediatrics, Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
Cell Transplant. 2008;17(9):1005-14.
Islet transplantation into the portal vein is the current clinical practice. However, it has now been recognized that this implantation site has several characteristics that can hamper islet engraftment and survival, such as low oxygen tension, an active innate immune system, and the provocation of an inflammatory response (IBMIR). These factors result in the loss of many transplanted islets, mainly during the first hours or days after transplantation, which could in part explain the necessity for the transplantation of islets from multiple pancreas donors to cure type 1 diabetes. This increases the burden on the limited pool of donor organs. Therefore, an alternative anatomical site for islet transplantation that offers maximum engraftment, efficacious use of produced insulin, and maximum patient safety is urgently needed. In this review, the experience with alternative sites for islet implantation in clinical and experimental models is discussed. Subcutaneous transplantation guarantees maximum patient safety and has become clinically applicable. Future improvements could be achieved with innovative designs for devices to induce neovascularization and protect the islets from cellular rejection. However, other sites, such as the omentum, offer drainage of produced insulin into the portal vein for direct utilization in the liver. The use of pigs would not only overcome the shortage of transplantable islets, but genetic modification could result in the expression of human genes, such as complement regulatory or "anticoagulation" genes in the islets to overcome some site-specific disadvantages. Eventually, the liver will most likely be replaced by a site that allows long-term survival of islets from a single donor to reverse type 1 diabetes.
将胰岛移植到门静脉是目前的临床实践。然而,现在已经认识到,这个植入部位有几个可能妨碍胰岛植入和存活的特征,如低氧张力、活跃的先天免疫系统以及引发炎症反应(即刻血液介导的炎症反应)。这些因素导致许多移植的胰岛丧失,主要是在移植后的最初几个小时或几天内,这在一定程度上可以解释为什么需要移植来自多个胰腺供体的胰岛来治愈1型糖尿病。这增加了有限供体器官库的负担。因此,迫切需要一个替代的胰岛移植解剖部位,该部位能提供最大程度的植入、有效利用产生的胰岛素并确保患者的最大安全。在这篇综述中,讨论了在临床和实验模型中胰岛植入替代部位的经验。皮下移植确保了患者的最大安全,并且已经在临床上得到应用。未来通过创新设计的装置诱导新血管形成并保护胰岛免受细胞排斥,可能会取得进一步的进展。然而,其他部位,如大网膜,可将产生的胰岛素引流到门静脉,以便在肝脏中直接利用。使用猪不仅可以克服可移植胰岛的短缺,而且基因改造可能导致胰岛中表达人类基因,如补体调节或“抗凝”基因,以克服一些特定部位的缺点。最终,肝脏很可能会被一个能使来自单个供体的胰岛长期存活以逆转1型糖尿病的部位所取代。