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在接受环孢素治疗的患者的白细胞中,钙调神经磷酸酶的活性仅受到部分抑制。

Calcineurin activity is only partially inhibited in leukocytes of cyclosporine-treated patients.

作者信息

Batiuk T D, Pazderka F, Halloran P F

机构信息

Department of Medicine, University of Alberta, Edmonton, Canada.

出版信息

Transplantation. 1995 May 27;59(10):1400-4. doi: 10.1097/00007890-199505270-00007.

Abstract

Measurement of the degree of immunosuppression induced clinically by drugs such as cyclosporine is an important but elusive goal. In lymphocytes in vitro, cyclosporine (CsA) blocks the phosphatase activity of the enzyme calcineurin, preventing cytokine induction. We sought to measure the degree of calcineurin blockade in patients on CsA. Calcineurin activity was measured in peripheral blood mononuclear cells (PBL) from stable CsA-treated renal transplant patients, compared with controls. Cytokine expression was assessed by challenging ex vivo PBL with calcium ionophore A23187 (5 microM) for 60 min and measuring interferon-gamma (IFN-gamma) and interleukin 2 (IL-2) mRNA induction. In vitro, CsA inhibited both calcineurin activity and cytokine induction with an IC50 of 10-20 micrograms/L. In CsA-treated patients with therapeutic CsA levels (mean trough CsA blood level = 180 +/- 55 micrograms/L), calcineurin activity was detectable but reduced by 50% compared with controls (P < or = 0.001) and correlated with CsA trough levels (r = -0.390, P < or = 0.01). The induction of cytokine mRNA in such patients was not blocked, but was sensitive to CsA in vitro, suggesting that CsA is much less available in vivo in body fluids than it is for isolated cells in vitro. In lymphocytes of patients on CsA, calcineurin activity is reduced but 50% of the activity persists, permitting strong signals to trigger cytokine expression. Partial calcineurin inhibition may explain why the immune responsiveness of patients on CsA is reduced but still sufficient for host defense.

摘要

测量环孢素等药物在临床上所诱导的免疫抑制程度是一个重要但难以实现的目标。在体外淋巴细胞中,环孢素(CsA)可阻断钙调神经磷酸酶的磷酸酶活性,从而阻止细胞因子的诱导。我们试图测量服用CsA患者体内钙调神经磷酸酶的阻断程度。对稳定接受CsA治疗的肾移植患者外周血单个核细胞(PBL)中的钙调神经磷酸酶活性进行了测量,并与对照组进行比较。通过用钙离子载体A23187(5 microM)对离体PBL进行60分钟的刺激,并测量干扰素-γ(IFN-γ)和白细胞介素2(IL-2)mRNA的诱导情况来评估细胞因子的表达。在体外,CsA以10 - 20微克/升的半数抑制浓度(IC50)抑制钙调神经磷酸酶活性和细胞因子诱导。在接受CsA治疗且CsA水平处于治疗范围(CsA血药谷浓度均值 = 180 ± 55微克/升)的患者中,可检测到钙调神经磷酸酶活性,但与对照组相比降低了50%(P≤0.001),且与CsA谷浓度相关(r = -0.390,P≤0.01)。此类患者中细胞因子mRNA的诱导未被阻断,但在体外对CsA敏感,这表明CsA在体内体液中的可利用性远低于其在体外对分离细胞的可利用性。在服用CsA患者的淋巴细胞中,钙调神经磷酸酶活性降低,但仍有50%的活性存在,这使得强信号能够触发细胞因子表达。钙调神经磷酸酶的部分抑制可能解释了为何服用CsA患者的免疫反应性降低但仍足以进行宿主防御。

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