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肾移植患者侵袭性真菌感染的外源性干扰素-γ免疫治疗。

Exogenous interferon-gamma immunotherapy for invasive fungal infections in kidney transplant patients.

机构信息

Department of Infectious Diseases and Immunity, Imperial College, London, UK.

出版信息

Am J Transplant. 2010 Aug;10(8):1796-803. doi: 10.1111/j.1600-6143.2010.03094.x. Epub 2010 Mar 26.

Abstract

The incidence of invasive fungal infections (IFIs) in nonneutropenic solid organ transplant patients is increasing. We report our clinical experience with the use of interferon-gamma (IFN-gamma) immunotherapy in seven renal transplant patients who developed life threatening, disseminated IFIs refractory to conventional antifungal drug therapy. The infections were all microbiologically and histologically proven. The rapid cure of these disseminated infections with exogenous IFN-gamma injections was not associated with impaired kidney allograft function despite the use of liposomal amphotericin B in all cases. No clinical toxicity from the IFN-gamma immunotherapy was seen and no IFI relapsed during long-term follow-up. Our experience is both uncontrolled and in patients with unpredictable fungal infection-related outcomes. However, compared to standard approaches, the accelerated cure of life threatening, disseminated IFIs with 6 weeks of combination antifungal drug therapy and IFN-gamma immunotherapy saved lives, retained allograft function and led to substantial cost savings in this small patient group.

摘要

非中性粒细胞减少的实体器官移植患者侵袭性真菌感染(IFI)的发病率正在增加。我们报告了在 7 例发生危及生命的播散性 IFI 且对常规抗真菌药物治疗耐药的肾移植患者中使用干扰素-γ(IFN-γ)免疫疗法的临床经验。所有感染均经微生物学和组织学证实。尽管所有病例均使用脂质体两性霉素 B,但外源性 IFN-γ 注射迅速治愈这些播散性感染,并未导致肾移植功能受损。IFN-γ 免疫疗法无临床毒性,且在长期随访中无 IFI 复发。我们的经验是不受控制的,且患者的真菌感染相关结局不可预测。然而,与标准方法相比,在 6 周的联合抗真菌药物治疗和 IFN-γ 免疫疗法的快速治愈危及生命的播散性 IFI 挽救了生命,保留了移植物功能,并在这一小患者群体中节省了大量成本。

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