Human herpesvirus-6B infection in pediatric allogenic hematopoietic stem cell transplant patients: Risk factors and encephalitis

被引:8
作者
Miura, Hiroki [1 ]
Kawamura, Yoshiki [1 ]
Hattori, Fumihiko [1 ]
Tanaka, Makito [1 ]
Kudo, Kazuko [1 ]
Ihira, Masaru [2 ]
Yatsuya, Hiroshi [3 ]
Takahashi, Yoshiyuki [4 ]
Kojima, Seiji [4 ]
Sakaguchi, Hirotoshi [5 ]
Yoshida, Nao [5 ]
Hama, Asahito [5 ]
Yoshikawa, Tetsushi [1 ]
机构
[1] Fujita Hlth Univ, Sch Med, Dept Pediat, Toyoake, Aichi, Japan
[2] Fujita Hlth Univ, Sch Hlth Sci, Fac Clin Engn, Toyoake, Aichi, Japan
[3] Fujita Hlth Univ, Sch Med, Dept Publ Hlth, Toyoake, Aichi, Japan
[4] Nagoya Univ, Grad Sch Med, Dept Pediat, Nagoya, Aichi, Japan
[5] Japanese Red Cross Nagoya First Hosp, Childrens Med Ctr, Dept Hematol & Oncol, Nagoya, Aichi, Japan
关键词
encephalitis; HHV-6; HSCT; risk factor; ACUTE LIMBIC ENCEPHALITIS; CORD BLOOD TRANSPLANTATION; HHV-6; ENCEPHALITIS; VIRAL LOAD; HUMAN-HERPESVIRUS-6; REACTIVATION; CEREBROSPINAL-FLUID; PREEMPTIVE THERAPY; CLINICAL-FEATURES; OUTCOMES; VIREMIA;
D O I
10.1111/tid.13203
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Human herpesvirus-6B (HHV-6B) infection after allogenic hematopoietic stem cell transplantation (allo-HSCT) is known to be associated with post-transplant limbic encephalitis in adults. Meanwhile, the association between HHV-6B infection and central nervous system complications remains unclear in pediatric allo-HSCT patients. Methods In this study, HHV-6B infection was monitored for more than 50 days after HSCT using virus isolation and real-time PCR. Clinical information such as patient background and encephalitis status was collected retrospectively from medical records. Risk factors for HHV-6B infection were determined by the Cox proportional hazards model, and the clinical features of HHV-6B encephalitis in pediatric allo-HSCT patients were elucidated. Results Human herpesvirus-6B infection was observed in 74 (33.8%) of 219 patients at 3-47 days (median 18, interquartile range 13-20). Risk factors identified in multivariable analysis were hematological malignancy (hazards ratio [HR], 5.0; 95% confidence interval [CI], 2.3/12.5; P < .0001), solid tumor (HR, 4.8; CI, 1.5/16.3; P = .0104), unrelated donor (HR, 2.1; CI, 1.0/4.6; P = .0378), and sex-mismatched donor (HR 1.8; CI, 1.1/3.0; P = .0257). HHV-6B encephalitis occurred in only one of the 219 patients (0.46%); this patient demonstrated the typical clinical course of posterior reversible encephalopathy syndrome. Conclusion Hematological malignancy, solid tumor, unrelated donor, and sex-mismatched donor were significant risk factors for HHV-6B infection after pediatric allo-HSCT. In pediatric allo-HSCT patients, the incidence of HHV-6B encephalitis was low and the clinical features differed from those in adult patients.
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页数:9
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