scholarly journals Hepatitis E virus infection in a hematopoietic stem cell donor

2013 ◽  
Vol 49 (1) ◽  
pp. 159-160 ◽  
Author(s):  
C Koenecke ◽  
S Pischke ◽  
G Beutel ◽  
U Ritter ◽  
A Ganser ◽  
...  
2019 ◽  
Vol 119 ◽  
pp. 31-36 ◽  
Author(s):  
Sara Cruz ◽  
Carla Campos ◽  
Mafalda Timóteo ◽  
Ana Tavares ◽  
Maria São José Nascimento ◽  
...  

2015 ◽  
Vol 71 (1) ◽  
pp. 141-144 ◽  
Author(s):  
Pierre Frange ◽  
Anne-Marie Roque-Afonso ◽  
Bénédicte Neven ◽  
Despina Moshous ◽  
Fabien Touzot ◽  
...  

Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 5734-5734
Author(s):  
Fei-Fei Tang ◽  
Xiao-Dong Mo ◽  
Yu Wang ◽  
Chen-Hua Yan ◽  
Yu-Hong Chen ◽  
...  

Abstract Introduction: Hepatitis E virus (HEV) is increasingly found to cause hepatitis in allogeneic hematopoietic stem cell transplantation (HSCT) patients. However, little is known about HEV infection in patients treated with haploidentical HSCT (haplo-HSCT). Here, we retrospectively evaluate the incidence and clinical course of HEV infection in haplo-HSCT patients. Methods: From January 2014 to July 2017, 177 patients with unexplained elevated transaminases after receiving haplo-HSCT at Peking University Institute of Haematology were screened for HEV infection using HEV serology. HEV RNA were performed when HEV-IgG and/or IgM antibodies were positive. Results: Acute HEV infection was identified in seven of these patients (3.9%), none of whom had developed a chronic HEV infection. The median time from haplo-HSCT to HEV infection was 17.5 (range, 6-55) months. Median peak alanine transaminase during HEV infection was 716 (range, 164-1763) U/L. In 7 cases, HEV infection was confirmed by the presentation of anti-HEV IgM + anti-HEV IgG (rising) (n=5) or HEV-RNA + anti-HEV IgM + anti-HEV IgG (n=2). None patients died of HEV infection directly. Two patients with HEV infection died showing signs of ongoing hepatitis and the median duration of HEV infection was 2.7 months. Five patients cleared HEV and the median duration of HEV infection was 1.5 (range, 1.0-5.7) months. Conclusions: In conclusion, HEV infection is a rare but serious complication after haplo-HSCT. We recommend screening of HEV infection in haplo-HSCT. Disclosures No relevant conflicts of interest to declare.


Blood ◽  
2013 ◽  
Vol 122 (6) ◽  
pp. 1079-1086 ◽  
Author(s):  
Jurjen Versluis ◽  
Suzan D. Pas ◽  
Hendrik J. Agteresch ◽  
Robert A. de Man ◽  
Jolanda Maaskant ◽  
...  

Abstract Hepatitis E virus (HEV) is increasingly acknowledged as a cause of hepatitis in healthy individuals as well as immunocompromised patients. Little is known of HEV infection in recipients of allogeneic hematopoietic stem cell transplantation (alloHSCT). Therefore, we set out to study the incidence and sequelae of HEV as a cause of hepatitis in a recent cohort of 328 alloHSCT recipients. HEV RNA was tested in episodes of liver enzyme abnormalities. In addition, HEV RNA and HEV serology were assessed pre- and post-alloHSCT. We found 8 cases (2.4%) of HEV infection, of which 5 had developed chronic HEV infection. Seroprevalence pre-alloHSCT was 13%. Four patients died with HEV viremia, with signs of ongoing hepatitis, having a median time of infection of 4.1 months. The 4 surviving patients cleared HEV after a median period of 6.3 months. One patient was diagnosed with HEV reactivation after a preceding infection prior to alloHSCT. Although the incidence of developing acute HEV post-alloHSCT is relatively low, the probability of developing chronic hepatitis in severely immunocompromised patients is high. Therefore, alloHSCT recipients should be screened pretransplantation by HEV serology and RNA. Furthermore, a differential diagnosis including hepatitis E is mandatory in all alloHSCT patients with severe liver enzyme abnormalities.


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