High incidence of human herpesvirus 6 infection with a high viral load in cord blood stem cell transplant recipients
Adult
0301 basic medicine
Transplantation Conditioning
Adolescent
Herpesvirus 6, Human
Incidence
Hematopoietic Stem Cell Transplantation
Infant
Roseolovirus Infections
Viral Load
Fetal Blood
Polymerase Chain Reaction
3. Good health
Survival Rate
03 medical and health sciences
Child, Preschool
DNA, Viral
Humans
Transplantation, Homologous
Virus Activation
Child
DOI:
10.1182/blood.v100.6.2005
Publication Date:
2019-10-14T04:48:09Z
AUTHORS (14)
ABSTRACT
AbstractHuman herpesvirus 6 (HHV-6) infection in recipients of cord blood stem cell transplants (CBSCTs) was estimated by semiquantitative and real-time quantitative polymerase chain reaction (PCR) and reverse-transcription PCR. Of the CBSCT recipients, 7 (70%) of 10 had active HHV-6 infection after transplantation, and all 7 were inferred from their age to have already had a primary infection. Because HHV-6 DNA is seldom detected in cord blood, these cases were considered likely to represent reactivation. In contrast, the 3 patients without HHV-6 infection were all believed to be naive regarding HHV-6 primary infection because of their age and the results of PCR assays given before the transplantation procedure. The incidence of HHV-6 infection after transplantation was significantly higher (P < .05) than after bone marrow (BM) transplantation and peripheral blood stem cell (PBSC) transplantation, when recipients without primary HHV-6 infection prior to transplantation were excluded (CBSCT, 100%; BMT/PBSCT, 56.3%). Real-time PCR revealed a higher level of viral DNA in the peripheral blood mononuclear cells from CBSCT recipients than from BMT/PBSCT recipients or patients with exanthem subitum (P < .05). HHV-6 mRNA of the U79/80gene was also detected by reverse-transcription PCR in all analyzed patients with HHV-6 infection. Its detection was correlated with the emergence of viral DNA in the plasma and symptoms such as fever and rash. Thus, HHV-6 infection was more frequent and the viral load was higher in CBSCT recipients with prior primary infection.
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