Wiederkehr J C, Dumble L, Pollak R, Moran M
Department of Surgery, University of Illinois, Chicago 60612.
Aust N Z J Surg. 1990 Feb;60(2):121-4.
Prostaglandins are reported to play an important regulatory role in cell-mediated immunity. The immunosuppressive properties of a new synthetic oral prostaglandin E1 analogue, misoprostol, were studied in vivo in a rat heterotopic cardiac allograft model, and in vitro in mixed lymphocyte reaction. The results show that parenteral misoprostol, alone or in combination with low dose cyclosporin immunosuppressive therapy, significantly prolonged cardiac allograft survival compared with appropriate controls. Oral misoprostol alone in this model did not allow for measurable cardiac allograft prolongation. In vitro misoprostol demonstrated significant dose-response inhibition of the mixed lymphocyte culture assay. It is concluded that new prostaglandin E1 analogues with oral bioavailability may have important applications to clinical transplantation in man, and may be cyclosporin sparing.
据报道,前列腺素在细胞介导的免疫中起重要的调节作用。在大鼠异位心脏同种异体移植模型中对一种新的合成口服前列腺素E1类似物米索前列醇的免疫抑制特性进行了体内研究,并在混合淋巴细胞反应中进行了体外研究。结果表明,与适当的对照组相比,肠外给予米索前列醇,单独或与低剂量环孢素免疫抑制疗法联合使用,可显著延长心脏同种异体移植的存活时间。在该模型中单独口服米索前列醇并不能使心脏同种异体移植的存活时间得到可测量的延长。体外实验中,米索前列醇在混合淋巴细胞培养试验中表现出显著的剂量反应抑制作用。结论是,具有口服生物利用度的新型前列腺素E1类似物可能在人类临床移植中具有重要应用,并且可能减少环孢素的使用。