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伊拉克肾移植患者移植前抗人类白细胞抗原抗体检测的临床相关性

Clinical Relevance of Pretransplant Testing for Anti-Human Leukocyte Antigen Antibodies in Iraqi Renal Transplant Patients.

作者信息

Ali Ala, Al-Kaisi Aroub, Ali Iqbal

机构信息

From the Nephrology and Renal Transplant Centre, The Medical City, Baghdad, Iraq.

出版信息

Exp Clin Transplant. 2019 Jan;17(Suppl 1):164-168. doi: 10.6002/ect.MESOT2018.P40.

Abstract

OBJECTIVES

The use of highly sensitive Luminex technology to assess the immunologic risk of renal transplant candidates have greatly added to the ability of stratifying patients and have paved the way to avoid hyperacute antibody-mediated rejection. Our aim was to understand how much the testing for pretransplant anti-HLA antibodies affects the decision for transplant and survival at 1 year posttransplant.

MATERIALS AND METHODS

From January 2014 to June 2017, 336 transplant candidates were tested by complement-dependent cytotoxicity and by the Luminex platform for anti-HLA antibodies in our nephrology and renal transplant center (The Medical City, Baghdad, Iraq). All clinical and laboratory data were noted. Our program is a living-donor, blood group-compatible donor program. All transplant patients (sensitized or not) were followed for 1 year, and the Kaplan-Meier method was used to determine survival rate.

RESULTS

Mean age of the study group was 34.07 ± 12.4 years. Of 336 transplant patients who were tested, there were 63 (18.75%) sensitized patients and 159 (47.35%) nonsensitized patients. Blood transfusion was the main cause of sensitization. Class I anti-HLA antibodies were detected in 54 of 63 sensitized patients (85.7%), and class II anti-HLA antibodies were detected in 39 of 63 sensitized patients (61.9%). Donor-specific antibodies were detected in 33/63 (52.3%). Thirteen sensitized patients (15.3%) underwent transplant. No incidences of hyperacute rejection were recorded. The 1-year survival of the nonsensitized patient group was 90%, whereas survival was 61.5% for the sensitized patient group.

CONCLUSIONS

Pretransplant testing for anti-HLA antibodies is undoubtedly useful for assessment of patient risk, to facilitate decisions regarding patient and donor selection, and to plan treatment strategies. The 1-year survival for sensitized patient was lower than for nonsensitized patients. More knowledge, experience, technology advancements, and support are needed to improve the Iraqi practice of transplanting sensitized patients.

摘要

目的

使用高灵敏度的Luminex技术评估肾移植候选者的免疫风险,极大地增强了对患者进行分层的能力,并为避免超急性抗体介导的排斥反应铺平了道路。我们的目的是了解移植前抗HLA抗体检测对移植决策及移植后1年生存率的影响程度。

材料与方法

2014年1月至2017年6月,在我们的肾脏病与肾移植中心(伊拉克巴格达医学城),对336名移植候选者进行了补体依赖细胞毒性试验以及使用Luminex平台检测抗HLA抗体。记录所有临床和实验室数据。我们的项目是一个活体供者、血型匹配的供者项目。所有移植患者(无论是否致敏)均随访1年,采用Kaplan-Meier法确定生存率。

结果

研究组的平均年龄为34.07±12.4岁。在接受检测的336名移植患者中,有63名(18.75%)致敏患者和159名(47.35%)非致敏患者。输血是致敏的主要原因。在63名致敏患者中,54名(85.7%)检测到I类抗HLA抗体,39名(61.9%)检测到II类抗HLA抗体。33/63(52.3%)检测到供者特异性抗体。13名致敏患者(15.3%)接受了移植。未记录到超急性排斥反应事件。非致敏患者组的1年生存率为90%,而致敏患者组的生存率为61.5%。

结论

移植前检测抗HLA抗体无疑有助于评估患者风险,便于做出关于患者和供者选择的决策,并制定治疗策略。致敏患者的1年生存率低于非致敏患者。需要更多的知识、经验、技术进步和支持来改善伊拉克对致敏患者进行移植的实践。

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