Akdeniz University Hospital, Department of Internal Medicine, Antalya, Turkey.
Akdeniz University Hospital, Department of Internal Medicine, Division of Nephrology, Antalya, Turkey.
Acta Clin Croat. 2023 Aug;62(2):262-269. doi: 10.20471/acc.2023.62.02.02.
The antibodies directed against human leukocyte antigen (HLA) molecules, which play a crucial role in allograft histocompatibility, are called anti-HLA antibodies. Anti-HLA antibodies against foreign HLA molecules may be present in patients with chronic kidney disease even before transplantation. The panel reactive antibody (PRA) test is used to measure the renal transplant candidate's immune sensitivity to HLA molecules other than their own HLA molecules by assessing the diversity of anti-HLA antibodies in the blood of these patients. This study aimed to determine the PRA values and the percentage of PRA positivity of Turkish male patients with chronic kidney disease (CKD), who had not been sensitized by the major known causes (those with no history of organ or tissue transplantation, those with no history of blood transfusion), who had not been diagnosed with any autoimmune diseases, and who had not been under immunosuppressive treatment. The study included 60 male patients aged over 18 years. All of the patients were followed up with a diagnosis of CKD at the Nephrology Clinic, Internal Medicine Department, Akdeniz University Medical Faculty Hospital. None of the patients included in the study was sensitized by a known mechanism previously (they did not have blood transfusion or organ transplantation). Glomerular filtration rate (GFR) levels of all patients were below the level of 60 mL/min/1.73 m. Patient data including their age information, etiology of CKD, accompanying diseases, and information about dialysis modalities were recorded. HLA antibody percentage was determined by the flow cytometry technique. Statistical data analysis was performed by using SPSS 22.0 (Statistical Package for Social Sciences, Version 22.0). The values of p less than 0.05 were considered statistically significant. Twenty patients were receiving dialysis treatment due to end-stage renal disease. Of the 60 patients included in the study, 25% showed PRA positivity; 28.3% of all study patients were found to be positive for anti-HLA class I antibodies and 26.7% of all study patients were found to be positive for anti-HLA class II antibodies on separate analysis for anti-HLA class I and anti-HLA class II antibody positivity. When the patients were categorized as PRA negative and PRA positive in two groups, there were no differences between the groups according to mean age, percentage of hemodialysis patients, percentage of peritoneal dialysis patients and presence of accompanying chronic diseases (such as hypertension, type 2 diabetes mellitus, hyperlipidemia, nephrolithiasis, coronary artery disease). In addition to this, evaluation of the GFR levels showed that the PRA positive group contained a significantly higher percentage of end-stage renal disease patients (GFR <15 mL/min/1.73 m) as compared with the PRA negative group. Detailed analysis of the percentages of PRA levels in the PRA positive patients, which was carried out to determine the degree of sensitization, showed that the PRA values were over 80% in 11.77% of the patients positive for anti-HLA class I antibodies. On the other hand, PRA values were within the range of 15%-80% in 88.23% of the patients who had anti-HLA class II antibodies. The PRA values were below 80% in all of the patients positive for anti-HLA class II antibodies and those positive for both anti-HLA class I and class II antibodies. In conclusion, PRA levels of the candidates for kidney transplantation should always be measured to assess their state of sensitization before transplantation, even though they have no risk factors known to cause anti-HLA antibody development.
针对人类白细胞抗原 (HLA) 分子的抗体在同种异体组织相容性中起着至关重要的作用,这些抗体被称为抗 HLA 抗体。患有慢性肾病的患者即使在移植前也可能存在针对外来 HLA 分子的抗 HLA 抗体。面板反应性抗体 (PRA) 测试用于通过评估这些患者血液中抗 HLA 抗体的多样性来测量肾移植候选者对除自身 HLA 分子以外的 HLA 分子的免疫敏感性。本研究旨在确定土耳其男性慢性肾病 (CKD) 患者的 PRA 值和 PRA 阳性率,这些患者未因主要已知原因(无器官或组织移植史、无输血史)而致敏,未被诊断为任何自身免疫性疾病,且未接受免疫抑制治疗。研究包括 60 名年龄在 18 岁以上的男性患者。所有患者均在阿克德尼兹大学医学系内科肾脏病诊所被诊断为 CKD 后进行随访。研究中纳入的患者均无先前已知机制致敏(无输血或器官移植史)。所有患者的肾小球滤过率 (GFR) 水平均低于 60 mL/min/1.73 m。记录了患者的年龄信息、CKD 的病因、伴随疾病以及透析方式的信息。通过流式细胞术技术确定 HLA 抗体百分比。使用 SPSS 22.0(社会科学统计软件包,版本 22.0)进行统计数据分析。p 值小于 0.05 被认为具有统计学意义。由于终末期肾病,有 20 名患者正在接受透析治疗。在纳入研究的 60 名患者中,有 25%表现出 PRA 阳性;28.3%的研究患者抗 HLA Ⅰ类抗体阳性,26.7%的研究患者抗 HLA Ⅱ类抗体阳性。当患者分为 PRA 阴性和 PRA 阳性两组时,两组之间的平均年龄、血液透析患者的百分比、腹膜透析患者的百分比和伴随慢性疾病(如高血压、2 型糖尿病、高脂血症、肾结石、冠心病)的存在情况无差异。此外,对 GFR 水平的评估表明,与 PRA 阴性组相比,PRA 阳性组中终末期肾病患者的比例显著更高(GFR <15 mL/min/1.73 m)。对 PRA 阳性患者的 PRA 水平百分比进行了详细分析,以确定致敏程度,结果显示,抗 HLA Ⅰ类抗体阳性患者中有 11.77%的患者的 PRA 值超过 80%。另一方面,抗 HLA Ⅱ类抗体阳性患者中有 88.23%的患者的 PRA 值在 15%-80%之间。所有抗 HLA Ⅱ类抗体阳性和同时抗 HLA Ⅰ类和Ⅱ类抗体阳性的患者的 PRA 值均低于 80%。总之,即使候选者没有已知导致抗 HLA 抗体产生的风险因素,在移植前也应始终测量肾移植候选者的 PRA 水平,以评估其致敏状态。