Kordower J H, Freeman T B, Snow B J, Vingerhoets F J, Mufson E J, Sanberg P R, Hauser R A, Smith D A, Nauert G M, Perl D P
Department of Neurological Sciences, Rush-Presbyterian-St. Luke's Medical Center, Chicago, IL 60612, USA.
N Engl J Med. 1995 Apr 27;332(17):1118-24. doi: 10.1056/NEJM199504273321702.
Trials are under way to determine whether fetal nigral grafts can improve motor function in patients with Parkinson's disease. Some studies use fluorodopa uptake on positron-emission tomography (PET) as a marker of graft viability, but fluorodopa uptake does not distinguish between host and grafted neurons. There has been no direct evidence that grafts of fetal tissue can survive and innervate the striatum.
We studied a 59-year-old man with advanced Parkinson's disease who received bilateral grafts of fetal ventral mesencephalic tissue in the postcommissural putamen. The tissue came from seven embryos between 6 1/2 and 9 weeks after conception. The patient died 18 months later from a massive pulmonary embolism. The brain was studied with the use of tyrosine hydroxylase immunohistochemical methods.
After transplantation, the patient had sustained improvement in motor function and a progressive increase in fluorodopa uptake in the putamen on PET scanning. On examination of the brain, each of the large grafts appeared to be viable. Each was integrated into the host striatum and contained dense clusters of dopaminergic neurons. Processes from these neurons had grown out of the grafts and provided extensive dopaminergic reinnervation to the striatum in a patch-matrix pattern. Ungrafted regions of the putamen showed sparse dopaminergic innervation. We could not identify any sprouting of host dopaminergic processes.
Grafts of fetal mesencephalic tissue can survive for a long period in the human brain and restore dopaminergic innervation to the striatum in patients with Parkinson's disease. In the patient we studied, clinical improvement and enhanced fluorodopa with uptake on PET scanning were associated the survival of the grafts and dopaminergic reinnervation of the striatum.
正在进行试验以确定胎儿黑质移植能否改善帕金森病患者的运动功能。一些研究使用正电子发射断层扫描(PET)上的氟多巴摄取作为移植存活的标志物,但氟多巴摄取无法区分宿主神经元和移植神经元。尚无直接证据表明胎儿组织移植能够存活并支配纹状体。
我们研究了一名59岁的晚期帕金森病男性患者,其在连合后壳核接受了双侧胎儿腹侧中脑组织移植。组织来自受孕后6.5至9周的7个胚胎。患者18个月后死于大面积肺栓塞。使用酪氨酸羟化酶免疫组化方法对大脑进行研究。
移植后,患者运动功能持续改善,PET扫描显示壳核中氟多巴摄取逐渐增加。对大脑进行检查时,每个大的移植物似乎都存活。每个移植物都整合到宿主纹状体中,并包含密集的多巴胺能神经元簇。这些神经元的突起从移植物中生长出来,并以斑块 - 基质模式为纹状体提供广泛的多巴胺能再支配。壳核未移植区域显示多巴胺能神经支配稀疏。我们未发现宿主多巴胺能突起有任何发芽现象。
胎儿中脑组织移植可在人脑中长期存活,并恢复帕金森病患者纹状体的多巴胺能神经支配。在我们研究的患者中,临床改善和PET扫描上氟多巴摄取增加与移植物存活及纹状体多巴胺能再支配有关。