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在围手术期使用兔抗胸腺细胞球蛋白(即胸腺球蛋白)进行淋巴细胞清除后,采用他克莫司单一疗法进行肠道移植。

Intestinal transplantation under tacrolimus monotherapy after perioperative lymphoid depletion with rabbit anti-thymocyte globulin (thymoglobulin).

作者信息

Reyes Jorge, Mazariegos George V, Abu-Elmagd Kareem, Macedo Camila, Bond Geoffrey J, Murase Noriko, Peters John, Sindhi Rakesh, Starzl Thomas E

机构信息

Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Thomas E. Starzl Transplantation Institute, USA.

出版信息

Am J Transplant. 2005 Jun;5(6):1430-6. doi: 10.1111/j.1600-6143.2005.00874.x.

Abstract

Modifications in the timing and dosage of immunosuppression can ameliorate the morbidity and mortality that has prevented widespread use of intestinal transplantation (ITx) in children. Thirty-six patients receiving ITx, aged 5 months to 20 years were given 2-3 mg(kg of rabbit anti-thymocyte globulin (rATG, thymoglobulin) just before ITx, and 2-3 mg(kg postoperatively (total 5 mg(kg). Twice daily doses of tacrolimus (TAC) were begun enterally within 24 h after graft reperfusion with reduction of dose quantity or frequency after 3 months. Prednisone or other agents were given to treat breakthrough rejection. After 8-28 months follow-up (mean 15.8 +/- 5.3), 1- and 2-year patient and graft survival is 100% and 94%, respectively. Despite a 44% incidence of acute rejection in the first month, 16 of the 34 (47%) survivors are on TAC (n = 14) or sirolimus (n = 2) monotherapy; 15 receive TAC plus low dose prednisone; one each receive TAC plus sirolimus, TAC plus azathioprine and TAC plus sirolimus and prednisone. There was a low incidence of immunosuppression-related complications. This strategy of immunosuppression minimized maintenance TAC exposure, facilitated the long-term control of rejection, decreased the incidence of opportunistic infections, and resulted in a high rate of patient and graft survival.

摘要

免疫抑制时机和剂量的调整可改善发病率和死亡率,这些问题曾阻碍儿童肠移植(ITx)的广泛应用。36例接受ITx的患者,年龄在5个月至20岁之间,在ITx前给予2 - 3mg/(kg)兔抗胸腺细胞球蛋白(rATG,即胸腺球蛋白),术后给予2 - 3mg/(kg)(总量5mg/(kg))。移植肾再灌注后24小时内开始经肠给予每日两次剂量的他克莫司(TAC),3个月后减少剂量或给药频率。给予泼尼松或其他药物治疗突破性排斥反应。经过8 - 28个月的随访(平均15.8±5.3),1年和2年的患者及移植肾存活率分别为100%和94%。尽管第一个月急性排斥反应发生率为44%,但34例(47%)存活者中有16例采用TAC(n = 14)或西罗莫司(n = 2)单药治疗;15例接受TAC加低剂量泼尼松;各有1例接受TAC加西罗莫司、TAC加硫唑嘌呤以及TAC加西罗莫司和泼尼松治疗。免疫抑制相关并发症的发生率较低。这种免疫抑制策略使维持期TAC暴露量最小化,便于长期控制排斥反应,降低了机会性感染的发生率,并导致了较高的患者及移植肾存活率。

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