Haddad H, MacNeil D M, Howlett J, O'Neill B
Queen Elizabeth II Health Sciences Centre, Halifax, Canada.
Can J Cardiol. 2000 Feb;16(2):221-4.
Rejection remains a major cause of both early and late morbidity and mortality following heart transplantation despite major advances in immunosuppressive therapy. A major hurdle in the successful management of patients who have undergone heart transplantation is preventing and treating graft rejection. Cyclosporine, mycophenolate mofetil, azathioprine, tacrolimus (FK506) and OKT3 are well documented, effective immunosuppressive medications that prevent and treat acute or chronic rejection following heart transplantation. One of the macrolide antibiotics, sirolimus, is known to have immunosuppressant activity. In two patients with chronic rejection of cardiac grafts refractory to usual antirejection medications, sirolimus was successfully used to suppress graft rejection. Both patients continued to be rejection free after 10 months of sirolimus treatment despite significant decreases in doses of other immunosuppressants.
尽管免疫抑制疗法取得了重大进展,但排斥反应仍然是心脏移植后早期和晚期发病及死亡的主要原因。成功管理心脏移植患者的一个主要障碍是预防和治疗移植物排斥反应。环孢素、霉酚酸酯、硫唑嘌呤、他克莫司(FK506)和OKT3是有充分文献记载的有效免疫抑制药物,可预防和治疗心脏移植后的急性或慢性排斥反应。大环内酯类抗生素之一西罗莫司已知具有免疫抑制活性。在两名常规抗排斥药物治疗无效的心脏移植物慢性排斥患者中,西罗莫司成功用于抑制移植物排斥反应。尽管其他免疫抑制剂剂量大幅降低,但两名患者在接受西罗莫司治疗10个月后仍未发生排斥反应。