Vol.:(0123456789) 1 3
Clinical Journal of Gastroenterology
https://doi.org/10.1007/s12328-019-01024-3
CASE REPORT
The spontaneous clearance of hepatitis E virus (HEV) and emergence
of HEV antibodies in a transfusion‑transmitted chronic hepatitis E case
after completion of chemotherapy for acute myeloid leukemia
Hiroshi Okano
1
· Tatsunori Nakano
2
· Ryugo Ito
3
· Ami Tanaka
4
· Yuji Hoshi
4
· Keiji Matsubayashi
4
·
Hiroki Asakawa
1
· Kenji Nose
1
· Satomi Tsuruga
1
· Tomomasa Tochio
1
· Hiroaki Kumazawa
1
· Yoshiaki Isono
1
·
Hiroki Tanaka
1
· Shimpei Matsusaki
1
· Tomohiro Sase
1
· Tomonori Saito
1
· Katsumi Mukai
1
· Akira Nishimura
1
·
Keiki Kawakami
3
· Shigeo Nagashima
5
· Masaharu Takahashi
5
· Hiroaki Okamoto
5
Received: 30 April 2019 / Accepted: 18 July 2019
© Japanese Society of Gastroenterology 2019
Abstract
A 64-year-old woman was infected with hepatitis E virus (HEV) during chemotherapy for leukemia. By retrospective analyses
of stored serum from the blood products and the patient, the source of the infection was determined to be platelet concentra-
tion (PC) transfused during chemotherapy. The partial nucleotide sequence of the HEV strain isolated from the donated PC
and that from the patient’s sera was identical and was subgenotype 3b. Clinical indicators such as alanine aminotransferase,
HEV RNA titer, and anti-HEV antibodies in the serum were investigated from the beginning of the infection until 1 year
after the termination of HEV infection. HEV RNA had propagated over 6 months and then cleared spontaneously after the
completion of chemotherapy. Anti-HEV antibodies appeared in the serum just before the clearance of HEV RNA. Interest-
ingly, HEV RNA was detected in the patient’s urine, spinal fluid, and saliva. The HEV RNA titers in those samples were
much lower than in the serum and feces. No renal, neurological, or salivary gland disorders appeared during the follow-up.
We observed virological and biochemical progress and cure of transfusion-transmitted chronic hepatitis E in the patient
despite an immunosuppressive status during and after chemotherapy against hematological malignancy.
Keywords Chemotherapy · Hepatitis E · Hematological malignancy · Immunosuppression · Transfusion
Introduction
Hepatitis E virus (HEV) infection causes hepatitis E out-
breaks in developing countries, where water sources are
sometimes contaminated by HEV. Hepatitis E virus also
causes sporadic and cluster cases of hepatitis E with char-
acteristics of zoonosis in developed countries [1, 2]. Blood-
borne transmission through the transfusion of blood products
contaminated with HEV is also an important transmission
route of HEV [3]. In Japan, 19 cases of transfusion-trans-
mitted hepatitis E have been reported [3].
Hepatitis E virus infection is diagnosed based on the pres-
ence of anti-HEV IgM/IgA and/or HEV RNA in the serum
of patients. It was reported that HEV infection under immu-
nosuppressive condition sometimes presents with prolonged
HEV viremia [4–8] and a delay or prevention of seroconver-
sion of anti-HEV antibodies [9]. However, data concerning
the long-term dynamics of HEV RNA and HEV-specific
Hiroshi Okano and Tatsunori Nakano contributed equally to this
work.
* Hiroshi Okano
oohh1969@yahoo.co.jp
1
Department of Gastroenterology, Suzuka General Hospital,
1275-53 Yasuzuka-cho, Suzuka, Mie 513-8630, Japan
2
Department of Internal Medicine, Fujita Health University
Nanakuri Memorial Hospital, 424-1 Oodori-cho, Tsu,
Mie 514-1295, Japan
3
Department of Hematology and Oncology, Suzuka General
Hospital, 1275-53 Yasuzuka-cho, Suzuka, Mie 513-8630,
Japan
4
Central Blood Institute, Blood Service Headquarters,
Japanese Red Cross Society, 1-1-3 Shiba-Daimon,
Minato-ku, Tokyo 105-8521, Japan
5
Division of Virology, Department of Infection and Immunity,
Jichi Medical University School of Medicine, 3311-1
Yakushiji, Shimotsuke, Tochigi 329-0498, Japan