Cyclosporin A. Clinical Pharmacology and Therapeutic Potential
Overview
Authors
Affiliations
Cyclosporin A is a cyclical polypeptide of 11 amino acids, one of which is unique to the cyclosporins. First isolated as an antifungal agent, it has been shown to have marked immunomodulatory properties. These properties have meant that the drug can be used as an immunosuppressant to prevent the rejection of transplants, both of organs and bone marrows, as well as in the control of autoimmune diseases. It has already been shown to have a major clinical impact in the transplantation of kidneys, pancreas, liver, hearts, heart and lung and both compatible and incompatible bone marrow grafts. The drug acts by inhibiting that part of the immune system which relies on T cell proliferation, probably by interference with second signal controls. The clinical results so far achieved with cyclosporin A indicate that it has an important part to play in the future of immunosuppression. With better, more reliable, immunosuppressive controls, the possibility exists that transplantation of immunologically more susceptible organs could become a routine procedure providing a treatment to patient populations whose conditions had previously been considered incurable.
Leisengang S, Schedlowski M, Hadamitzky M, Luckemann L Curr Protoc. 2022; 2(10):e573.
PMID: 36219717 PMC: 11648820. DOI: 10.1002/cpz1.573.
The biosynthetic pathway of FK506 and its engineering: from past achievements to future prospects.
Ban Y, Park S, Yoon Y J Ind Microbiol Biotechnol. 2015; 43(2-3):389-400.
PMID: 26342319 DOI: 10.1007/s10295-015-1677-7.
Kimura S, Iyama S, Yamaguchi Y, Kanakura Y J Clin Lab Anal. 2002; 15(6):319-23.
PMID: 11793432 PMC: 6807697. DOI: 10.1002/jcla.1044.
Pahl H, Krauss B, Schulze-Osthoff K, Decker T, Traenckner E, Vogt M J Exp Med. 1996; 183(4):1829-40.
PMID: 8666939 PMC: 2192527. DOI: 10.1084/jem.183.4.1829.
The clearance of cyclosporine by hemodialysis.
Venkataramanan R, Ptachcinski R, Burckart G, Yang S, Starzl T, Van Theil D J Clin Pharmacol. 1984; 24(11-12):528-31.
PMID: 6392355 PMC: 2981080. DOI: 10.1002/j.1552-4604.1984.tb02763.x.