Stallone Giovanni, Schena Antonio, Infante Barbara, Di Paolo Salvatore, Loverre Antonella, Maggio Giulio, Ranieri Elena, Gesualdo Loreto, Schena Francesco Paolo, Grandaliano Giuseppe
Division of Nephrology, Department of Emergency and Transplantation, University of Bari, Bari, Italy.
N Engl J Med. 2005 Mar 31;352(13):1317-23. doi: 10.1056/NEJMoa042831.
Recipients of organ transplants are susceptible to Kaposi's sarcoma as a result of treatment with immunosuppressive drugs. Sirolimus (rapamycin), an immunosuppressive drug, may also have antitumor effects.
We stopped cyclosporine therapy in 15 kidney-transplant recipients who had biopsy-proven Kaposi's sarcoma and began sirolimus therapy. All patients underwent an excisional biopsy of the lesion and one biopsy of normal skin at the time of diagnosis. A second biopsy was performed at the site of a previous Kaposi's sarcoma lesion six months after sirolimus therapy was begun. We examined biopsy specimens for vascular endothelial growth factor (VEGF), Flk-1/KDR protein, and phosphorylated Akt and p70S6 kinase, two enzymes in the signaling pathway targeted by sirolimus.
Three months after sirolimus therapy was begun, all cutaneous Kaposi's sarcoma lesions had disappeared in all patients. Remission was confirmed histologically in all patients six months after sirolimus therapy was begun. There were no acute episodes of rejection or changes in kidney-graft function. Levels of Flk-1/KDR and phosphorylated Akt and p70S6 kinase were increased in Kaposi's sarcoma cells. The expression of VEGF was increased in Kaposi's sarcoma cells and even more so in normal skin cells around the Kaposi's sarcoma lesions.
Sirolimus inhibits the progression of dermal Kaposi's sarcoma in kidney-transplant recipients while providing effective immunosuppression.
由于接受免疫抑制药物治疗,器官移植受者易患卡波西肉瘤。西罗莫司(雷帕霉素)作为一种免疫抑制药物,可能也具有抗肿瘤作用。
我们对15例经活检证实患有卡波西肉瘤的肾移植受者停止环孢素治疗,并开始西罗莫司治疗。所有患者在诊断时均对病变进行了切除活检,并对正常皮肤进行了一次活检。在开始西罗莫司治疗6个月后,在先前卡波西肉瘤病变部位进行了第二次活检。我们检查了活检标本中的血管内皮生长因子(VEGF)、Flk-1/KDR蛋白以及磷酸化的Akt和p70S6激酶,这两种酶是西罗莫司作用的信号通路中的酶。
开始西罗莫司治疗3个月后,所有患者的皮肤卡波西肉瘤病变均消失。开始西罗莫司治疗6个月后,所有患者经组织学证实病情缓解。未出现急性排斥反应发作,肾移植功能也未发生变化。卡波西肉瘤细胞中Flk-1/KDR、磷酸化的Akt和p70S6激酶水平升高。卡波西肉瘤细胞中VEGF的表达增加,在卡波西肉瘤病变周围的正常皮肤细胞中增加更为明显。
西罗莫司在抑制肾移植受者皮肤卡波西肉瘤进展的同时,还能提供有效的免疫抑制作用。