Transfusion-Transmitted Hepatitis E Virus Infection in France

被引:49
|
作者
Gallian, Pierre [1 ,2 ]
Pouchol, Elodie [1 ,15 ]
Djoudi, Rachid [1 ]
Lhomme, Sebastien [3 ,4 ]
Mouna, Lina [5 ]
Gross, Sylvie [1 ]
Bierling, Philippe [6 ]
Assal, Azzedine [7 ]
Kamar, Nassim [8 ,9 ,10 ]
Mallet, Vincent [11 ,12 ,13 ]
Roque-Afonso, Anne-Marie [5 ]
Izopet, Jacques [3 ,4 ]
Tiberghien, Pierre [1 ,14 ]
机构
[1] Etab Francais Sang, 20 Ave Stade France, F-93218 La Plaine St Denis, France
[2] Univ Aix Marseille, INSERM, U1207, Unite Virus Emergents,IRD 90,IHU Mediterranee Inf, Marseille, France
[3] CHU Toulouse, Serv Virol, Ctr Natl Reference Virus Hepatite E, Toulouse, France
[4] CNRS, UMR 5282, INSERM, UMR 1043, Toulouse, France
[5] CHU Paul Brousse, AP HP, INSERM,Serv Virol, U1193,Ctr Natl Reference Hepatites Transmiss Ente, Villejuif, France
[6] Etab Francais Sang Ile France, Creteil, France
[7] Etab Francais Sang Nouvelle Aquitaine, Bordeaux, France
[8] CHU Rangueil, Dept Nephrol & Transplantat Organe, Toulouse, France
[9] Ctr Physiopathol Toulouse Purpan, INSERM, UMR1043, Toulouse, France
[10] Univ Paul Sabatier, Toulouse, France
[11] Univ Paris 05, Sorbonne Paris Cite, Paris, France
[12] Inst Pasteur, INSERM 1223, Paris, France
[13] Cochin Port Royal, AP HP, Serv Hepatol, Paris, France
[14] Univ Franche Comte, INSERM, UMR 1098, Etab Francais Sang, Besancon, France
[15] Minist Sante, Direct Gen Sante, Paris, France
关键词
Hepatitis E; Hepatitis E virus; Transfusion-transmitted infection; ORGAN-TRANSPLANT RECIPIENTS; BLOOD-DONATIONS; TRANSMISSION; PREVALENCE; DONORS;
D O I
10.1016/j.tmrv.2019.06.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 'IT 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. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:146 / 153
页数:8
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