Abdel Rahman Afaf S, Fahim Nehal M A, El Sayed Abeer A, El Hady Soha A R, Ahmad Yasser S
Department of Microbiology & Immunology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Egypt J Immunol. 2005;12(2):77-89.
Renal transplantation, in most countries, is based on human leukocyte antigen (HLA) matching of the donor kidney with the recipient. Traditional human leukocyte antigen matching is based on defining human leukocyte antigen specificities by antibodies utilizing cytotoxicity crossmatch techniques. Newer techniques have emerged, which challenge the accuracy of serological typing and crossmatching. We compared the results of the standard complement-dependent cytotoxicity crossmatch (CDCXM) with the anti-human globulin augmented cytotoxicity (AHG-CDC), and Flowcytometry crossmatch (FCXM) for the detection of anti-HLA antibodies in 150 pre-transplant patients. The development of post-transplantation sensitization was screened utilizing these three techniques within two weeks post-operative and correlated with rejection episodes. Comparison between the results of CDCXM and AHG-CDC in 150 recipients, revealed no significant correlation (P>0.05). When comparing these results with that of FCXM in 50 recipients a significant correlation was shown (P<0.05). Relative to CDCXM, the sensitivity of AHG-CDC was 100%, specificity 97.4%, positive predictive value 92.3%, and negative predictive value 100%. On the other hand, the sensitivity of FCXM was 100%, specificity 76.3%, positive predictive value 57.1%, and negative predictive value 100%. According to the results of CDCXM, AHG-CDC, and FCXM, no difference was detected between pre- and posttransplant anti-HLA sensitization within two weeks after the operation. Patients with negative cytotoxicity crossmatch (CDCXM and AHG-CDC) and positive FCXM may have an increased risk of early graft loss and may represent a relative contraindication to transplantation. Given the important theoretical advantages of FCXM over the CDC XM, further testing of the clinical relevance is warranted.
在大多数国家,肾移植是基于供体肾脏与受体的人类白细胞抗原(HLA)匹配进行的。传统的人类白细胞抗原匹配是通过利用细胞毒性交叉配型技术的抗体来确定人类白细胞抗原特异性。更新的技术已经出现,这些技术对血清学分型和交叉配型的准确性提出了挑战。我们比较了标准补体依赖细胞毒性交叉配型(CDCXM)、抗人球蛋白增强细胞毒性(AHG-CDC)和流式细胞术交叉配型(FCXM)在150例移植前患者中检测抗HLA抗体的结果。在术后两周内利用这三种技术筛查移植后致敏的发生情况,并与排斥反应相关联。150例受体中CDCXM和AHG-CDC结果的比较显示无显著相关性(P>0.05)。在50例受体中将这些结果与FCXM结果进行比较时,显示出显著相关性(P<0.05)。相对于CDCXM,AHG-CDC的敏感性为100%,特异性为97.4%,阳性预测值为92.3%,阴性预测值为100%。另一方面,FCXM的敏感性为100%,特异性为76.3%,阳性预测值为57.1%,阴性预测值为100%。根据CDCXM、AHG-CDC和FCXM的结果,术后两周内移植前和移植后抗HLA致敏情况未检测到差异。细胞毒性交叉配型(CDCXM和AHG-CDC)阴性而FCXM阳性的患者可能早期移植物丢失风险增加,可能代表移植的相对禁忌证。鉴于FCXM相对于CDCXM具有重要的理论优势,有必要进一步测试其临床相关性。