Ata P, Canbakan M, Kara M, Özel L, Ünal E, Titiz M İ
Genetic Diseases Diagnosis Center, Molecular Genetics Laboratory, Haydarpasa Numune Research and Training Hospital, Istanbul, Turkey.
Transplant Proc. 2012 Jul-Aug;44(6):1652-5. doi: 10.1016/j.transproceed.2012.05.032.
Patients displaying flow cytometric crossmatch results within the grey zone of positivity are hard to evaluate, especially if they are undergoing their first transplantation. For these patients assays of donor-specific anti-HLA (human leukocyte antigen) antibodies with complement-fixing properties to cause cell lysis are important for antibody-mediated rejection and graft failure. The aim of this study was to detect the relevance of serum C1q-binding antibodies detected in renal recipients with grey zone crossmatch reactivity who were considered to show low levels of sensitization against their potential donors.
This study includes 114 patients who were admitted for their first renal transplantation between September 2009 and August 2011, including 33 subjects considered by flow cytometric cross-match to be the sensitized group, whereas the remaining 81 recipients had negative results. We analyzed the accumulation of serum the immunoglobulin (Ig)G bound C1q on HLA-coated flow cytometric panel reactive antibody (FlowPRA) beads. The serum samples were retrospectively analyzed with [C1q]FlowPRA (HLA class I and II), which were collected during the pretransplantation period every 6 months and every week posttransplantation within the first month and every 3 months thereafter. All serum samples were analyzed for the presence of anti-FlowPRA IgG alloantibody. We compared the C1q FlowPRA-positive and-negative groups for the number of posttransplantation days that the serum creatinine level was below <2 mg/dL as a metric of graft function.
With a mean follow-up of 492 ± 84 days, there was a significant difference between flow cytometric crossmatch results and creatinine decrease rate (P = .02). The serum creatinine decrease rates of the 9 C1q-positive versus the 15 C1q-negative subjects showed significant difference (P < .05).
C1q-binding antibody analysis shows the presence of serum antibodies capable of complement binding and antibody-mediated rejection, which could be useful to assess rejection risk among the "grey zone" of renal recipients with low levels of sensitization against their donors.
呈现流式细胞术交叉配型结果处于阳性灰色区域的患者难以评估,尤其是那些正在接受首次移植的患者。对于这些患者,检测具有补体固定特性以引起细胞裂解的供者特异性抗人白细胞抗原(HLA)抗体,对于抗体介导的排斥反应和移植失败至关重要。本研究的目的是检测在肾移植受者中检测到的血清C1q结合抗体的相关性,这些受者的交叉配型反应处于灰色区域,被认为对其潜在供者的致敏水平较低。
本研究纳入了2009年9月至2011年8月期间因首次肾移植入院的114例患者,其中33例经流式细胞术交叉配型被认为是致敏组,其余81例受者结果为阴性。我们分析了血清免疫球蛋白(Ig)G结合在HLA包被的流式细胞术群体反应性抗体(FlowPRA)微珠上的C1q的积累情况。回顾性分析血清样本的[C1q]FlowPRA(HLAⅠ类和Ⅱ类),这些样本在移植前每6个月采集一次,移植后第一个月每周采集一次,此后每3个月采集一次。所有血清样本均分析抗FlowPRA IgG同种抗体的存在情况。我们比较了C1q FlowPRA阳性和阴性组血清肌酐水平低于<2mg/dL的移植后天数,以此作为移植肾功能的指标。
平均随访492±84天,流式细胞术交叉配型结果与肌酐下降率之间存在显著差异(P = 0.02)。9例C1q阳性受试者与15例C1q阴性受试者的血清肌酐下降率显示出显著差异(P < 0.05)。
C1q结合抗体分析显示存在能够补体结合和抗体介导排斥反应的血清抗体,这对于评估对供者致敏水平较低的肾移植受者“灰色区域”中的排斥风险可能有用。