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停用钙调神经磷酸酶抑制剂后,霉酚酸酯逐渐减量会进一步损害供体导向的细胞毒性。

After discontinuation of calcineurin inhibitors, tapering of mycophenolate mofetil further impairs donor-directed cytotoxicity.

作者信息

van Besouw Nicole M, van de Wetering Jacqueline, van der Mast Barbara J, de Kuiper Ronella, Baan Carla C, Weimar Willem

机构信息

Department of Internal Medicine-Transplantation, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

出版信息

Clin Transplant. 2008 Mar-Apr;22(2):129-35. doi: 10.1111/j.1399-0012.2007.00754.x.

Abstract

BACKGROUND

Recently, we described a significant decrease in donor-specific cytotoxic T-lymphocyte precursor frequency (CTLpf) after discontinuation of calcineurin inhibitors (CNI), while the proliferative capacity in mixed lymphocyte culture (MLC), and the number of interferon-gamma (IFN-gamma) producing cells (pc) in Elispot remained unchanged.

METHODS

We tested T-cell reactivity in CNI free patients with stable renal graft function, on mycophenolate mofetil (MMF) or azathioprine (AZA) plus prednisone, who were tapered to 50% of their MMF or AZA dose.

RESULTS

Furthermore, tapering of the MMF or AZA dose resulted in a decrease of donor-reactive CTLpf in all patients with detectable CTLpf. Detectable numbers decreased from a median of 32 to 8 CTLp/10(6) peripheral blood mononuclear cell (PBMC). No effect on third-party reactive CTLpf was found, while the T-cell reactivity to donor and third-party cells as tested in MLC and in IFN-gamma Elispot was not affected either by tapering of immunosuppression. Third-party reactivity was significantly higher than donor-specific reactivity in all tests. A control group showed no changes in any of the in vitro assays.

CONCLUSION

Both withdrawal of CNI and tapering of MMF or AZA dose decreases the donor-specific CTLpf. Our data suggest that reduction of immunosuppression results in a specific decrease of donor-directed cytotoxic capacity of immunocompetent cells, while their proliferation and cytokine production capacity remained unchanged. Immunosuppression hinders development of cytotoxic non-responsiveness.

摘要

背景

最近,我们描述了停用钙调神经磷酸酶抑制剂(CNI)后供体特异性细胞毒性T淋巴细胞前体频率(CTLpf)显著降低,而混合淋巴细胞培养(MLC)中的增殖能力以及酶联免疫斑点试验(Elispot)中产生干扰素-γ(IFN-γ)的细胞数量(pc)保持不变。

方法

我们测试了肾移植功能稳定、正在使用霉酚酸酯(MMF)或硫唑嘌呤(AZA)加泼尼松的无CNI患者的T细胞反应性,这些患者的MMF或AZA剂量减至50%。

结果

此外,MMF或AZA剂量的减少导致所有可检测到CTLpf的患者中供体反应性CTLpf降低。可检测数量从中位数32降至8个CTLp/10⁶外周血单个核细胞(PBMC)。未发现对第三方反应性CTLpf有影响,而在MLC和IFN-γ Elispot中测试的对供体细胞和第三方细胞的T细胞反应性也不受免疫抑制减量的影响。在所有测试中第三方反应性均显著高于供体特异性反应性。一个对照组在任何体外试验中均未显示变化。

结论

停用CNI以及MMF或AZA剂量的减少均会降低供体特异性CTLpf。我们的数据表明,免疫抑制的减少导致免疫活性细胞的供体定向细胞毒性能力特异性降低,而它们的增殖和细胞因子产生能力保持不变。免疫抑制阻碍细胞毒性无反应性的发展。

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