Unit of Infectious Diseases, Hospital Universitario "12 de Octubre," Instituto de Investigación Hospital "12 de Octubre" (imas12), Madrid, Spain.
Department of Nephrology, Hospital Universitario "12 de Octubre," Instituto de Investigación Hospital "12 de Octubre" (imas12), Madrid, Spain.
J Infect Dis. 2020 Jul 6;222(3):479-487. doi: 10.1093/infdis/jiaa090.
We aimed at constructing a composite score based on Epstein-Barr virus DNAemia (EBVd) and simple clinical and immunological parameters to predict late severe infection (LI) beyond month 6 in solid organ transplantation (SOT) recipients.
Kidney and liver transplant recipients between May 2014 and August 2016 at 4 participating centers were included. Serum immunoglobulins and complement factors, peripheral blood lymphocyte subpopulations, and whole blood EBVd were determined at months 1, 3, and 6. Cox regression analyses were performed to generate a weighted score for the prediction of LI.
Overall, 309 SOT recipients were followed-up for a median of 1000 days from transplant (interquartile range, 822-1124). Late severe infection occurred in 104 patients (33.6%). The CLIV Score consisted of the following variables at month 6: high-level EBVd (>1500 IU/mL) and recurrent infection during the previous months (6 points); recipient age ≥70 years and chronic graft dysfunction (5 points); cytomegalovirus mismatch (4 points); and CD8+ T-cell count <400 cells/μL (2 points). The area under receiver operating characteristics curve was 0.77 (95% confidence interval, 0.71-0.84). The risk of LI at day 1000 was as follows: score 0, 12.6%; score 2-5, 25.5%; score 6-9, 52.7%; score ≥10, 73.5%.
While waiting for further external validation, the CLIV Score based on clinical and immune-virological parameters is potentially useful to stratify the risk of LI after SOT.
本研究旨在构建一种基于 EBV 病毒血症(EBVd)和简单的临床及免疫参数的复合评分,以预测实体器官移植(SOT)受者 6 个月后晚期严重感染(LI)。
2014 年 5 月至 2016 年 8 月,4 个参与中心的肾和肝移植受者被纳入研究。在移植后第 1、3 和 6 个月检测血清免疫球蛋白和补体因子、外周血淋巴细胞亚群和全血 EBVd。采用 Cox 回归分析生成用于预测 LI 的加权评分。
共 309 例 SOT 受者接受了中位时间为 1000 天(四分位距,822-1124)的随访。104 例患者(33.6%)发生晚期严重感染。CLIV 评分由第 6 个月的以下变量组成:高水平 EBVd(>1500 IU/mL)和前几个月的复发性感染(6 分);受者年龄≥70 岁和慢性移植物功能障碍(5 分);巨细胞病毒不匹配(4 分);以及 CD8+T 细胞计数<400 个/μL(2 分)。受试者工作特征曲线下面积为 0.77(95%置信区间,0.71-0.84)。第 1000 天 LI 的风险如下:评分 0,12.6%;评分 2-5,25.5%;评分 6-9,52.7%;评分≥10,73.5%。
虽然还需要进一步的外部验证,但基于临床和免疫病毒学参数的 CLIV 评分可能有助于分层 SOT 后 LI 的风险。