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[三联或四联免疫抑制治疗下肾移植后的感染]

[Infections following kidney transplantation under threefold or fourfold immunosuppressive treatment].

作者信息

Hancke E, Schleibner S, Schneeberger H, Illner W D, Land W

机构信息

Abteilung für Transplantationschirurgie, Klinikum Grosshadern der Universität München.

出版信息

Dtsch Med Wochenschr. 1990 Mar 23;115(12):443-6. doi: 10.1055/s-2008-1065027.

DOI:10.1055/s-2008-1065027
PMID:2318113
Abstract

To determine, whether the infection rate after renal transplantation is influenced by the intensity of immunosuppressive treatment, the postoperative course of 100 consecutive renal transplantations in 64 men and 36 women (mean age 44.1 [18-72] years) was investigated prospectively. 87 patients received threefold basal immunosuppression with low-dose ciclosporin, azathioprine and prednisolone. In 13 risk patients (retransplantation and [or] high panel-reactive antibody titres), poly- or monoclonal antibodies were administered additionally to prevent rejection. Steroid-resistant rejection crises had to be treated with poly- or monoclonal antibodies in 15 patients. Postoperatively there were 10 patients with systemic infections (5 with cytomegalovirus, 4 with herpes simplex virus and 1 with Pneumocystis carinii). The infection rate with three- or fourfold immunosuppression did not differ significantly (5.4% vs. 9.1%). However, infections occurred more frequently after additional antirejection treatment with poly- or monoclonal antibodies (33%). It is concluded from these results that fourfold basal immunosuppression treatment with poly- or monoclonal antibodies is not associated with an increased risk of perioperative infections.

摘要

为了确定肾移植后的感染率是否受免疫抑制治疗强度的影响,我们对64名男性和36名女性(平均年龄44.1岁[18 - 72岁])连续进行的100例肾移植患者的术后病程进行了前瞻性研究。87例患者接受了低剂量环孢素、硫唑嘌呤和泼尼松龙的三联基础免疫抑制治疗。13例高危患者(再次移植和/或高群体反应性抗体滴度)额外给予了多克隆或单克隆抗体以预防排斥反应。15例患者出现类固醇抵抗性排斥反应危机,必须用多克隆或单克隆抗体进行治疗。术后有10例患者发生全身感染(5例为巨细胞病毒感染,4例为单纯疱疹病毒感染,1例为卡氏肺孢子虫感染)。三联或四联免疫抑制治疗的感染率无显著差异(5.4%对9.1%)。然而,在额外使用多克隆或单克隆抗体进行抗排斥治疗后,感染更频繁发生(33%)。从这些结果得出结论,使用多克隆或单克隆抗体进行四联基础免疫抑制治疗与围手术期感染风险增加无关。

相似文献

1
[Infections following kidney transplantation under threefold or fourfold immunosuppressive treatment].[三联或四联免疫抑制治疗下肾移植后的感染]
Dtsch Med Wochenschr. 1990 Mar 23;115(12):443-6. doi: 10.1055/s-2008-1065027.
2
Infection and rejection of primary hepatic transplant in 93 consecutive patients treated with triple immunosuppressive therapy.
Surg Gynecol Obstet. 1988 Dec;167(6):474-84.
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Infectious complications after simultaneous pancreas-kidney transplantation.胰肾联合移植后的感染性并发症
Transplant Proc. 2005 Oct;37(8):3560-3. doi: 10.1016/j.transproceed.2005.09.078.
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Renal allograft immunosuppression. II. A randomized trial of withdrawal of one drug in triple drug immunosuppression.
Transpl Int. 1990 Oct;3(3):121-7.
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A randomized, placebo-controlled trial with anti-interleukin-2 receptor antibody for immunosuppressive induction therapy after liver transplantation.一项关于抗白细胞介素-2受体抗体用于肝移植后免疫抑制诱导治疗的随机、安慰剂对照试验。
Clin Transplant. 1998 Aug;12(4):303-12.
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[Value of a powerful initial immunosuppression after liver transplantation. Prospective study of 60 cases].[肝移植后强效初始免疫抑制的价值。60例前瞻性研究]
Gastroenterol Clin Biol. 1994;18(2):115-22.
7
Low-dose ciclosporin, prednisone, and azathioprine after initial immunosuppression with ciclosporin and prednisone in a pediatric renal transplant population.在儿科肾移植人群中,初始使用环孢素和泼尼松进行免疫抑制后,给予低剂量环孢素、泼尼松和硫唑嘌呤。
Child Nephrol Urol. 1990;10(3):125-30.
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Effective prevention of interstitial rejection crises in immunological high risk patients following renal transplantation: use of high doses of the new monoclonal antibody BMA 031.肾移植后免疫高风险患者间质性排斥反应危机的有效预防:高剂量新型单克隆抗体BMA 031的应用
Transplant Proc. 1990 Aug;22(4):1789-90.
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A prospective comparison of murine monoclonal CD-3 (OKT3) antibody-based and equine antithymocyte globulin-based rejection prophylaxis in cardiac transplantation. Decreased rejection and less corticosteroid use with OKT3.心脏移植中基于鼠单克隆CD-3(OKT3)抗体和基于马抗胸腺细胞球蛋白的排斥反应预防措施的前瞻性比较。使用OKT3可降低排斥反应并减少皮质类固醇的使用。
Transplantation. 1989 Apr;47(4):599-605.
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Renal transplantation at Hartford Hospital: results of combined and flexible immunosuppression.
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