Hasse C, Schlosser A, Klöck G, Barth P, Stinner B, Zimmermann U, Rothmund M
Klinik für Allgemeinchirurgie, Philipps-Universität Marburg, Baldingerstrasse, 35043 Marburg, Deutschland.
Langenbecks Arch Chir Suppl Kongressbd. 1998;115(Suppl I):713-8.
The role of parathyroid transplantation for the therapy of permanent hypoparathyroidism is undisputed. Because the parathyroid hormone deficiency syndromee rarely every is a vital thread to patients affected, systemic immunosuppression for transplant recipients is not justified. A technique of microencapsulation was modified for transplantation of parathyroid tissue. Using a core substance suitable for clinical use (amitogenic alginate), we accomplished allotransplantation of functioning parathyroid tissue in the long-term animal model and, very recently, reported first clinical cases without postoperative immunosuppression. In a controlled animal model of totally parathyroidectomized rats (PTX, two groups of n = 40), we investigated the ability of microencapsulation with the amitogenic alginate to enable transplantation across the highest immunological barrier (xenotransplantation: human-rat); to ensure intact transplant function and to protect from rejection. Rat parathyroid hormone (PTHRA i.S.) and serum calcium levels served as parameters of completeness of PTX; intact human PTH (PTHRA i.S.) and serum calcium levels of recipient animals were used to assess graft function. Also, tissue integrity within explanted capsules was assessed by histology. Cultured and microencapsulated parathyroid tissue resumes and maintains function in vivo, even if transplanted across the highest immunological barrier. Functionally, PTHHU i.S. replaced (PTHRA i.S.) in PTX animals entirely and restored normocalcemia. These results suggest, that xeno-transplantation of the parathyroids can be achieved without postoperative immuno-suppression in a long term animal model. These data also imply the possibility of clinical heterotransplantation of parathyroid glands.
甲状旁腺移植在永久性甲状旁腺功能减退治疗中的作用是无可争议的。由于甲状旁腺激素缺乏综合征很少成为影响患者的关键因素,因此对移植受者进行全身免疫抑制是不合理的。一种微囊化技术被改进用于甲状旁腺组织移植。使用适合临床使用的核心物质(致免疫惰性藻酸盐),我们在长期动物模型中成功进行了功能性甲状旁腺组织的同种异体移植,并且最近报道了首例术后无需免疫抑制的临床病例。在完全甲状旁腺切除大鼠(PTX,两组,每组n = 40)的对照动物模型中,我们研究了用致免疫惰性藻酸盐进行微囊化实现跨越最高免疫屏障(异种移植:人 - 大鼠)移植的能力;确保移植功能完整并防止排斥反应。大鼠甲状旁腺激素(PTHRA i.S.)和血清钙水平作为PTX完整性的参数;受体动物的完整人甲状旁腺激素(PTHRA i.S.)和血清钙水平用于评估移植物功能。此外,通过组织学评估取出胶囊内的组织完整性。培养并微囊化的甲状旁腺组织在体内恢复并维持功能,即使跨越最高免疫屏障进行移植。在功能上,PTHHU i.S.完全替代了PTX动物中的(PTHRA i.S.)并恢复了正常血钙水平。这些结果表明,在长期动物模型中,甲状旁腺异种移植可以在术后无需免疫抑制的情况下实现。这些数据还暗示了甲状旁腺临床异种移植的可能性。