Suppr超能文献

免疫抑制、嗜酸性粒细胞趋化因子以及早期急性心脏移植排斥反应之前嗜酸性粒细胞的诊断性变化。

Immunosuppression, eotaxin and the diagnostic changes in eosinophils that precede early acute heart allograft rejection.

作者信息

Trull Andrew K, Akhlaghi Fatemeh, Charman Susan C, Endenberg Sylvia, Majid Oneeb, Cornelissen Jacqueline, Steel Louise, Parameshwar Jayan, Wallwork John, Large Stephen

机构信息

Department of Clinical Pharmacology, Papworth Hospital, Cambridge CB3 8RE, UK.

出版信息

Transpl Immunol. 2004 Jan;12(2):159-66. doi: 10.1016/S0966-3274(03)00077-7.

Abstract

Peripheral blood eosinophil counts (EOS) are undetectable in 40% blood samples sent for routine haematology at Papworth Hospital during the first 3 months after heart transplantation (HTx). Increases in EOS usually precede the development of allograft rejection by a median of 4 days. We compared the effects of cyclosporin (dose and total blood concentration), prednisolone (dose and both total and unbound plasma concentrations) and azathioprine, as well as plasma concentrations of the CCR-3 chemokines, eotaxin and RANTES, on changes in EOS in 47 consecutive HTx recipients, with a median follow-up of 90 (IQR 85-95) days. Multivariate analysis confirmed the independent association between both prednisolone dose (P<0.0001) and eotaxin (P<0.0001) and changes in EOS. The plasma eotaxin concentration was, in turn, most closely associated with the cyclosporin dose (P<0.001) and plasma prednisolone concentration (P=0.022). The blood cyclosporin concentration (P=0.028), EOS (P=0.012) and prednisolone dose (P=0.015) were all independently associated with the risk of treated acute rejection. When prednisolone pharmacokinetic parameters were substituted for the prednisolone dose in this multivariate model, only the pharmacokinetic parameter retained a significant association with the risk of rejection. Changes in EOS preceding cardiac allograft rejection are directly associated with plasma eotaxin concentrations and indirectly with prednisolone dosage. Cyclosporin may also indirectly influence these changes by inhibiting eotaxin production. EOS, prednisolone dose and blood cyclosporin concentrations were independently associated with the risk of acute rejection. The total and unbound fractions of prednisolone in plasma appear to be even more closely related to rejection but are difficult to measure. Monitoring EOS, as a surrogate measure of prednisolone immunosuppression, may be more cost-effective for controlling rejection than conventional cyclosporin monitoring in the first 6 weeks after HTx.

摘要

在心脏移植(HTx)后的前3个月内,Papworth医院送检的常规血液学检查血样中,40%的外周血嗜酸性粒细胞计数(EOS)无法检测到。EOS升高通常在同种异体移植排斥反应发生前出现,中位时间为4天。我们比较了环孢素(剂量和全血浓度)、泼尼松龙(剂量以及总血浆浓度和游离血浆浓度)和硫唑嘌呤,以及CCR-3趋化因子、嗜酸性粒细胞趋化蛋白和调节激活正常T细胞表达和分泌因子(RANTES)的血浆浓度,对47例连续HTx受者EOS变化的影响,中位随访时间为90(四分位间距85 - 95)天。多变量分析证实泼尼松龙剂量(P<0.0001)和嗜酸性粒细胞趋化蛋白(P<0.0001)与EOS变化之间存在独立关联。血浆嗜酸性粒细胞趋化蛋白浓度又与环孢素剂量(P<0.001)和血浆泼尼松龙浓度(P = 0.022)最为密切相关。血中环孢素浓度(P = 0.028)、EOS(P = 0.012)和泼尼松龙剂量(P = 0.015)均与治疗性急性排斥反应风险独立相关。当在该多变量模型中用泼尼松龙药代动力学参数替代泼尼松龙剂量时,只有药代动力学参数与排斥反应风险保持显著关联。心脏同种异体移植排斥反应前EOS的变化与血浆嗜酸性粒细胞趋化蛋白浓度直接相关,与泼尼松龙剂量间接相关。环孢素也可能通过抑制嗜酸性粒细胞趋化蛋白的产生间接影响这些变化。EOS、泼尼松龙剂量和血中环孢素浓度与急性排斥反应风险独立相关。血浆中泼尼松龙的总分数和游离分数似乎与排斥反应的关系更为密切,但难以测量。在HTx后的前6周,监测EOS作为泼尼松龙免疫抑制的替代指标,对于控制排斥反应可能比传统的环孢素监测更具成本效益。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验