Etablissement Français du Sang, La Plaine St Denis, France; Unité des virus émergents (Université Aix-Marseille, IRD 90, U 1207 Inserm), IHU Méditerranée Infection, Marseille, France.
Etablissement Français du Sang, La Plaine St Denis, France.
Transfus Med Rev. 2019 Jul;33(3):146-153. doi: 10.1016/j.tmrv.2019.06.001. Epub 2019 Jun 20.
There is growing concern regarding the risk of transfusion- transmitted (TT) hepatitis E. Since the first described case in 2006, several TT hepatitis E have been reported to the French hemovigilance network. We performed a retrospective analysis of all cases of TT hepatitis E reported between 2006 and 2016. Transfusion-transmitted hepatitis E with high imputability according to phylogenetic analysis occurred in 23 patients aged 8 to 88 years and involved mostly solid organ recipients (n = 9) or patients with malignant hematological diseases (n = 9, including 4 hematopoietic allograft recipients). Involved blood products were plasma (n = 7), among which 6 had undergone pathogen reduction with solvent/detergent (n = 4) or amotosalen + ultra-violet A (UVA) (n = 2 from 1 donation) treatments, red blood concentrates (n = 7), apheresis platelets concentrates (n = 3) and whole blood pooled platelets concentrates (n = 6), among which one had underwent amotosalen + UVA treatment. Median hepatitis E virus (HEV) RNA dose infused was 5.79 [4.36-10.10] log IU. HEV infection progressed to chronic hepatitis E in 14 (61%) immunocompromised patients, 2 of whom had advanced liver fibrosis at diagnosis. Chronic hepatitis E patients cleared HEV with ribavirin treatment (n = 10), after immunosuppressive drug reduction (n = 3), or spontaneously (n = 1). One additional organ transplant recipient with associated co-morbidities died with ongoing HEV infection and multiple organ failure. The other 8 (34.8%) patients with TT hepatitis E cleared HEV within 6 months with ribavirin treatment (n = 3), reduced immunosuppression (n = 1) or spontaneously (n = 4). Red cells, platelets, and plasma transfusions may be associated with TT hepatitis E that can evolve to chronic hepatitis E in immunocompromised patients. Hepatitis E virus has emerged in France as a clinically significant TT infection risk.
人们越来越关注输血传播(TT)型戊型肝炎的风险。自 2006 年首例病例描述以来,法国血液监测网络已报告了几例 TT 型戊型肝炎病例。我们对 2006 年至 2016 年期间报告的所有 TT 型戊型肝炎病例进行了回顾性分析。根据系统进化分析,23 例年龄 8 至 88 岁的患者发生高致病性 TT 型戊型肝炎,这些患者主要为实体器官受者(n=9)或恶性血液系统疾病患者(n=9,包括 4 例造血干细胞移植受者)。涉及的血液制品有血浆(n=7),其中 6 例采用了溶剂/去污剂(n=4)或光照加氨基酮戊酸(UVA)(n=2,来自 1 份供体)处理进行病原体灭活,浓缩红细胞(n=7)、单采血小板(n=3)和混合血小板浓缩物(n=6),其中 1 例采用了光照加氨基酮戊酸处理。输注的戊型肝炎病毒(HEV)RNA 剂量中位数为 5.79[4.36-10.10]logIU。14 例免疫功能低下的患者(61%)发展为慢性戊型肝炎,其中 2 例在诊断时已有晚期肝纤维化。慢性戊型肝炎患者用利巴韦林治疗清除 HEV(n=10)、减少免疫抑制药物(n=3)或自发清除(n=1)。1 例合并其他合并症的器官移植受者,由于 HEV 感染和多器官衰竭而死亡。另外 8 例(34.8%)TT 型戊型肝炎患者,6 个月内用利巴韦林治疗(n=3)、减少免疫抑制药物(n=1)或自发清除(n=4)清除 HEV。红细胞、血小板和血浆输注可能与 TT 型戊型肝炎有关,免疫功能低下患者可进展为慢性戊型肝炎。戊型肝炎病毒在法国已成为一种具有临床意义的 TT 感染风险。