Department of Nephrology and Organ Transplantation, CHU Rangueil, Toulouse, France; Université Paul Sabatier, Toulouse, France.
Am J Transplant. 2014 Apr;14(4):867-75. doi: 10.1111/ajt.12651. Epub 2014 Mar 1.
Although large retrospective studies have identified the presence of donor-specific antibodies (DSAs) to be a risk factor for rejection and impaired survival after liver transplantation, the long-term predicted pathogenic potential of individual DSAs after liver transplantation remains unclear. We investigated the incidence, prevalence and consequences of DSAs in maintenance liver transplant (LT) recipients. Two hundred sixty-seven LT recipients, who had undergone transplantation at least 6 months previously and had been screened for DSAs at least twice using single-antigen bead technology, were included and tested annually for the presence of DSAs. At a median of 51 months (min-max: 6-220) after an LT, 13% of patients had DSAs. At a median of 36.5 months (min-max: 2-45) after the first screening, 9% of patients have developed de novo DSAs. The sole predictive factor for the emergence of de novo DSAs was retransplantation (OR 3.75; 95% CI 1.28-11.05, p = 0.025). Five out of 21 patients with de novo DSAs (23.8%) developed an antibody-mediated rejection. Fibrosis score was higher among patients with DSAs. In conclusion, monitoring for the development of DSAs in maintenance LT patients is useful in case of graft dysfunction and to identify patients with a high risk of developing liver fibrosis.
尽管大型回顾性研究已经确定供体特异性抗体(DSA)的存在是肝移植后排斥反应和生存受损的危险因素,但肝移植后个体 DSA 的长期预测致病性潜力仍不清楚。我们研究了维持性肝移植(LT)受者中 DSA 的发生率、患病率和后果。267 名 LT 受者在至少 6 个月前接受移植,并且至少使用单抗原珠技术进行了两次 DSA 筛查,包括在内并每年检测 DSA 的存在情况。在 LT 后中位数为 51 个月(最小-最大:6-220)时,13%的患者有 DSA。在首次筛查后中位数为 36.5 个月(最小-最大:2-45)时,9%的患者出现了新的 DSA。新出现的 DSA 的唯一预测因素是再次移植(OR 3.75;95%CI 1.28-11.05,p = 0.025)。21 例新出现 DSA 的患者中有 5 例(23.8%)发生了抗体介导的排斥反应。DSA 患者的纤维化评分较高。总之,在移植功能障碍的情况下,监测维持性 LT 患者 DSA 的发展有助于识别具有发生肝纤维化高风险的患者。