PMID- 23723198 OWN - NLM STAT- MEDLINE DCOM- 20140310 LR - 20220408 IS - 1537-6591 (Electronic) IS - 1058-4838 (Linking) VI - 57 IP - 5 DP - 2013 Sep TI - Human herpesvirus 6 (HHV-6) reactivation and HHV-6 encephalitis after allogeneic hematopoietic cell transplantation: a multicenter, prospective study. PG - 671-81 LID - 10.1093/cid/cit358 [doi] AB - BACKGROUND: The epidemiology of human herpesvirus 6 (HHV-6) encephalitis after allogeneic hematopoietic cell transplantation (HCT) and its relationship with HHV-6 reactivation have not been sufficiently characterized. METHODS: This prospective, multicenter study of 230 allogeneic HCT recipients investigated the epidemiology of HHV-6 reactivation and HHV-6 encephalitis. Plasma HHV-6 DNA load was prospectively evaluated twice weekly until 70 days after HCT. RESULTS: Cumulative incidence of positive HHV-6 DNA and high-level HHV-6 reactivation (plasma HHV-6 DNA >/=10(4) copies/mL) at day 70 after HCT was 72.2% and 37.0%, respectively. Multivariate analysis identified myeloablative conditioning (hazard ratio [HR], 1.9; P = .004), umbilical cord blood transplantation (UCBT) (HR, 2.0; P = .003), and male sex (HR, 1.6; P = .04) as risk factors for displaying high-level HHV-6 reactivation. HHV-6 encephalitis occurred in 7 patients, and cumulative incidence at day 70 was 3.0%. None of the144 patients without high-level HHV-6 reactivation and 7 of 86 patients (8.1%) with high-level HHV-6 reactivation developed HHV-6 encephalitis (P = .0009). Prevalence of HHV-6 encephalitis was significantly higher among patients receiving UCBT than in patients with other sources (cumulative incidence at day 70, 7.9% vs 1.2%, P = .008). In each of 7 patients with HHV-6 encephalitis, central nervous system (CNS) symptoms developed concomitant with peak plasma HHV-6 DNA (range, 21 656-433 639 copies/mL). CONCLUSIONS: High levels of plasma HHV-6 DNA are associated with higher risk of HHV-6 encephalitis. UCBT is a significant risk factor for HHV-6 encephalitis. HHV-6 encephalitis should be considered if CNS dysfunction develops concomitant to high-level plasma HHV-6 DNA after allogeneic HCT. FAU - Ogata, Masao AU - Ogata M AD - Department of Hematology, Oita University Hospital, Hasama-machi, Yufu-city 879-5593, Japan. mogata@oita-u.ac.jp FAU - Satou, Takako AU - Satou T FAU - Kadota, Jun-ichi AU - Kadota J FAU - Saito, Noriyuki AU - Saito N FAU - Yoshida, Takashi AU - Yoshida T FAU - Okumura, Hirokazu AU - Okumura H FAU - Ueki, Toshimitsu AU - Ueki T FAU - Nagafuji, Koji AU - Nagafuji K FAU - Kako, Shinichi AU - Kako S FAU - Uoshima, Nobuhiko AU - Uoshima N FAU - Tsudo, Mitsuru AU - Tsudo M FAU - Itamura, Hidekazu AU - Itamura H FAU - Fukuda, Takahiro AU - Fukuda T LA - eng PT - Journal Article PT - Multicenter Study PT - Research Support, Non-U.S. Gov't DEP - 20130530 PL - United States TA - Clin Infect Dis JT - Clinical infectious diseases : an official publication of the Infectious Diseases Society of America JID - 9203213 RN - 0 (DNA, Viral) SB - IM MH - Adolescent MH - Adult MH - Aged MH - Cord Blood Stem Cell Transplantation/*adverse effects MH - DNA, Viral/blood MH - Encephalitis, Viral/*epidemiology/virology MH - Female MH - Herpesvirus 6, Human/*isolation & purification MH - Humans MH - Incidence MH - Male MH - Middle Aged MH - Prospective Studies MH - Roseolovirus Infections/*epidemiology/virology MH - Viral Load MH - *Virus Activation MH - Young Adult OTO - NOTNLM OT - HHV-6 encephalitis OT - HHV-6 reactivation OT - allogeneic hematopoietic cell transplantation OT - human herpesvirus 6 OT - viral load EDAT- 2013/06/01 06:00 MHDA- 2014/03/13 06:00 CRDT- 2013/06/01 06:00 PHST- 2013/06/01 06:00 [entrez] PHST- 2013/06/01 06:00 [pubmed] PHST- 2014/03/13 06:00 [medline] AID - cit358 [pii] AID - 10.1093/cid/cit358 [doi] PST - ppublish SO - Clin Infect Dis. 2013 Sep;57(5):671-81. doi: 10.1093/cid/cit358. Epub 2013 May 30.