Tedesco Dustin, Haragsim Lukas
Division of Nephrology and Hypertension, University of Oklahoma Health Sciences Center, 920 S. L. Young Blvd, WP 2250 Oklahoma City, OK 73104, USA.
J Transplant. 2012;2012:230386. doi: 10.1155/2012/230386. Epub 2012 Jan 4.
The discovery and use of cyclosporine since its inception into clinical use in the late 1970s has played a major role in the advancement of transplant medicine. While it has improved rates of acute rejection and early graft survival, data on long-term survival of renal allografts is less convincing. The finding of acute reversible nephrotoxicity and nephrotoxicity in nonrenal transplants has since led to the widely accepted view that there is a chronic more irreversible component to this agent as well. Since that time, there has been intense interest in finding protocols which seek to minimize and even avoid the use of calcineurin inhibitors altogether. We seek to review cyclosporine in terms of its mechanism of action, pathophysiologic, and histologic features associated with acute and chronic nephrotoxicity and recent studies looking to avoid its toxic side effects.
自20世纪70年代末环孢素开始临床应用以来,其发现和使用在移植医学的发展中发挥了重要作用。虽然它提高了急性排斥反应的发生率和早期移植物存活率,但关于肾移植长期存活的数据却不那么令人信服。此后,在非肾移植中发现了急性可逆性肾毒性和肾毒性,这导致了一种广泛接受的观点,即这种药物也存在慢性且更不可逆的成分。从那时起,人们就对寻找旨在尽量减少甚至完全避免使用钙调神经磷酸酶抑制剂的方案产生了浓厚兴趣。我们试图从环孢素的作用机制、与急性和慢性肾毒性相关的病理生理及组织学特征,以及近期旨在避免其毒副作用的研究等方面对其进行综述。