首页> 外文期刊>The Journal of heart and lung transplantation: the official publication of the International Society for Heart Transplantation >Does human leukocyte antigen matching influence the outcome of lung transplantation? An analysis of 3,549 lung transplantations.
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Does human leukocyte antigen matching influence the outcome of lung transplantation? An analysis of 3,549 lung transplantations.

机译:人白细胞抗原匹配会影响肺移植的结果吗?分析3,549例肺移植。

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BACKGROUND AND OBJECTIVE: Human leukocyte antigen (HLA) compatibility has been shown to improve the outcome of renal and cardiac transplantation. However, its impact on outcome following lung transplantation is not clear, with several single-center studies reporting inconsistent results. We studied the influence of HLA matching on survival and the development of rejection and obliterative bronchiolitis after lung transplantation, using data from the United Network for Organ Sharing/International Society for Heart and Lung Transplantation registry. METHODS: The study population included adult patients who received cadaveric lung transplants between October 1987 and June 1997 for whom HLA data were available. Two cohorts were examined, depending on the era of transplantation: (1) October 1987 to June 1997 (n = 3,549): Differences in actuarial survival as stratified by either the total number of HLA mismatches or the number of mismatches at each HLA locus were determined using a log-rank test. Multivariate logistic regression models were developed to determine independent predictors of survival at 1, 3, and 5 years following lung transplantation. (2) April 1994 to June 1997 (n = 1,796): The association of HLA mismatching with acute rejection and obliterative bronchiolitis was determined using a chi-squared analysis. RESULTS: Only 164 patients (4.6%) received lung grafts with 2 or fewer HLA mismatches. Univariate analyses demonstrated a significant difference in post-transplant survival by mismatch level, with the total number of HLA mismatches (p = 0.0008) and mismatching at the HLA-A locus (p = 0.002) associated with worse survival. Multivariate logistic regression demonstrated that the number of mismatches at the HLA-A and HLA-DR loci predicted 1-year mortality (incremental odds ratios 1.18, p = 0.01, and 1.15, p = 0. 03, respectively). The total number of HLA mismatches predicted 3- and 5-year mortality (incremental odds ratios 1.13 at 3 years, p = 0. 0004, and 1.14 at 5 years, p = 0.0002). However, other covariates such as repeat transplantation, transplantation for congenital heart disease, advanced recipient age, and an early era of transplantation were stronger predictors of mortality. We found no significant association between HLA mismatching and the development of obliterative bronchiolitis, although there was an association between mismatching at the HLA-A locus and acute rejection episodes requiring hospital admission (p = 0.008). We also found no association between mismatching at the HLA-B locus and rejection episodes requiring either hospitalization or the alteration of anti-rejection medications (p = 0.034). CONCLUSION: Although the number of HLA mismatches at the HLA-A and HLA-DR loci predicted 1-year mortality and the total number of mismatches predicted 3- and 5-year mortality following lung transplantation, the effect of each covariate was small in this multicenter study of 3,549 patients. Further close follow-up of registry patients is necessary to determine the effect of HLA matching on long-term survival and freedom from obliterative bronchiolitis and rejection following lung transplantation. A prospective study of HLA matching for lung transplantation should not yet be considered in view of the small number of grafts with 2 or fewer mismatches and the modest effect of HLA matching on outcome.
机译:背景与目的:人白细胞抗原(HLA)的相容性已被证明可以改善肾脏和心脏移植的疗效。但是,它对肺移植后预后的影响尚不清楚,一些单中心研究报告结果不一致。我们使用来自器官共享联合网络/国际心肺移植协会注册数据的数据,研究了HLA匹配对存活率以及肺移植后排斥反应和闭塞性细支气管炎发展的影响。方法:研究人群包括1987年10月至1997年6月间接受尸体肺移植的成年患者,这些患者可获得HLA数据。根据移植的时代,检查了两个队列:(1)1987年10月至1997年6月(n = 3,549):按照HLA失配总数或每个HLA所在地的失配数分层,精算存活率的差异为使用对数秩检验确定。建立了多变量逻辑回归模型,以确定肺移植后1年,3年和5年生存的独立预测因子。 (2)1994年4月至1997年6月(n = 1,796):使用卡方分析确定了HLA失配与急性排斥反应和闭塞性细支气管炎的相关性。结果:只有164例患者(4.6%)接受了2个或更少HLA不匹配的肺移植。单变量分析显示,在失配水平上,移植后存活率存在显着差异,HLA失配的总数(p = 0.0008)和HLA-A基因座的失配(p = 0.002)与较差的存活率相关。多元logistic回归表明,HLA-A和HLA-DR基因座的错配数目预测了1年死亡率(分别为1.18,p = 0.01和1.15,p = 0. 03)。 HLA不匹配的总数预测了3年和5年死亡率(3年时增加的比值比为1.13,p = 0。0004,5年时为1.14,p = 0.0002)。但是,其他协变量,例如重复移植,先天性心脏病移植,晚期接受者年龄和早期移植时代,是死亡率的更强预测指标。我们发现HLA失配与闭塞性细支气管炎的发展之间没有显着相关性,尽管HLA-A基因座的失配与需要住院的急性排斥反应之间存在关联(p = 0.008)。我们还发现在HLA-B位点的错配与需要住院或更换抗排斥药物的排斥发作之间没有关联(p = 0.034)。结论:尽管HLA-A和HLA-DR基因座的HLA错配数量预测了1年死亡率,而肺移植后3年和5年死亡率的错配总数预测了这一因素的影响很小。对3,549名患者的多中心研究。为了确定HLA匹配对长期生存以及肺移植后无闭塞性细支气管炎和排斥反应的影响,需要对注册患者进行进一步的密切随访。鉴于移植物数量少或错配不超过2个或更少,并且HLA匹配对结局的影响不大,因此尚未考虑对肺移植进行HLA匹配的前瞻性研究。

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