de Groen P C
Division of Gastroenterology and Internal Medicine, Mayo Clinic, Rochester, MD 59905.
Mayo Clin Proc. 1989 Jun;64(6):680-9. doi: 10.1016/s0025-6196(12)65348-8.
During the past decade, treatment with cyclosporine, an immunosuppressive agent, has contributed substantially to enhanced allograft and patient survival after liver transplantation. Currently, the 1-year survival rate after liver transplantation is more than 80% in major liver transplantation centers, in contrast with approximately 60% before the availability of cyclosporine. Its predominant immunologic effect is inhibition of lymphokine production and secretion by helper T cells. The use of cyclosporine, however, is associated with numerous adverse effects, the most important of which are nephrotoxicity, hypertension, neurotoxicity, opportunistic infections, and malignant lesions. Acute nephrotoxicity, hypertension, and neurotoxicity usually can be reversed by decreasing the dose of cyclosporine. Measurement of cyclosporine concentrations in the blood is essential for optimization of immunosuppressive therapy and prevention of toxicity.
在过去十年中,免疫抑制剂环孢素的应用极大地提高了肝移植后同种异体移植物的存活率和患者的生存率。目前,在主要的肝移植中心,肝移植后的1年生存率超过80%,而在环孢素问世之前约为60%。其主要的免疫作用是抑制辅助性T细胞产生和分泌淋巴因子。然而,使用环孢素会带来许多不良反应,其中最重要的是肾毒性、高血压、神经毒性、机会性感染和恶性病变。急性肾毒性、高血压和神经毒性通常可以通过降低环孢素的剂量来逆转。测定血液中环孢素的浓度对于优化免疫抑制治疗和预防毒性至关重要。