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HLA抗体和可溶性CD30与肾移植预后不良相关:一项单中心横断面研究的更新结果。

HLA antibodies and soluble CD30 are associated with poor renal graft outcome: updated results of a single-center cross-sectional study.

作者信息

Langan Leanne L, D'Orsogna Lloyd, Park Lawrence P, Hughes Tiffany L, Irish Ashley, Luxton Grant, Witt Campbell S, Christiansen Frank T

机构信息

Department of Clinical Immunology and Biochemical Genetics, PathWest, Royal Perth Hospital, Western Australia.

出版信息

Clin Transpl. 2006:219-25.

Abstract

In a previous study, we have shown that HLA class II antibodies and a high soluble CD30 (sCD30) measured at least 1 year post-transplant predict subsequent graft failure. We have now updated the results of this same cohort of 208 patients 15 months later. HLA-specific antibodies (class I and class II) were detected by ELISA LAT-M and Luminex LabScreen assays. Data on graft outcome was collected with a median follow-up of 4.7 years. By Kaplan-Meier analysis, class II antibody was again associated with a poorer outcome, with an estimated 6-year graft survival of 67% and 71% when detected by ELISA and Luminex, respectively, compared with 92% for those without class II antibody (p < or = 0.0001). A soluble CD30 level of > or = 100 U/ml was also associated with a poorer estimated 6-year graft survival (p = 0.02). HLA antibodies and high sCD30 (> or = 100 U/ml) had an additive effect such that those with both high sCD30 and class II antibodies had a hazard ratio for subsequent graft failure of 18.1 (p = 0.0008) and 8.6 (p = 0.007) when detected by ELISA and Luminex, respectively. These data show that detection of HLA class II antibodies and serum sCD30 measured at least 1 year post-transplant continues to predict a subsequent outcome up to 6 years after the initial measurement; they also show that such measures provide important information that may allow for modification of ongoing therapy.

摘要

在之前的一项研究中,我们已经表明,移植后至少1年检测到的HLA II类抗体和高可溶性CD30(sCD30)可预测随后的移植物失败。我们现在在15个月后更新了这同一组208例患者的结果。通过ELISA LAT - M和Luminex LabScreen检测法检测HLA特异性抗体(I类和II类)。收集移植物结局数据,中位随访时间为4.7年。通过Kaplan - Meier分析,II类抗体再次与较差的结局相关,通过ELISA和Luminex检测时,估计6年移植物存活率分别为67%和71%,而无II类抗体者为92%(p≤0.0001)。可溶性CD30水平≥100 U/ml也与较差的估计6年移植物存活率相关(p = 0.02)。HLA抗体和高sCD30(≥100 U/ml)具有相加作用,因此,同时具有高sCD30和II类抗体的患者,通过ELISA和Luminex检测时,随后移植物失败的风险比分别为18.1(p = 0.0008)和8.6(p = 0.007)。这些数据表明,移植后至少1年检测到的HLA II类抗体和血清sCD30在初始测量后长达6年仍可预测随后的结局;它们还表明,这些检测可提供重要信息,可能有助于调整正在进行的治疗。

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