HHV-6 infection after allogeneic hematopoietic stem cell transplantation: From chromosomal integration to viral co-infections and T-cell reconstitution patterns

Risk Adult Male 570 Patients Survival Adolescent [SDV]Life Sciences [q-bio] Herpesvirus 6, Human Virus Integration 610 Roseolovirus Infections [SDV.CAN]Life Sciences [q-bio]/Cancer CD8-Positive T-Lymphocytes methods immunology Young Adult 03 medical and health sciences Bone Marrow Risk Factors blood 616 Humans Transplantation, Homologous Aged 0303 health sciences Coinfection Hematopoietic Stem Cell Transplantation Viral Load Middle Aged virology 3. Good health Case-Control Studies Female Virus Activation France Infection Laboratories transplantation Stem Cell Transplantation
DOI: 10.1016/j.jinf.2015.09.039 Publication Date: 2015-10-30T18:01:39Z
ABSTRACT
Human herpes virus 6 (HHV-6) can reactivate after allogeneic hematopoietic stem cell transplantation (allo-HSCT) and may be associated with significant clinical manifestations.Case control study of HHV-6 infections after allo-HSCT. Chromosomal integration (ciHHV-6) for viral loads ≥ 5.5-log10 copies/mL was investigated. Viral co-infections, T-cell recovery, risk factors and outcome were compared in HHV-6- and non-HHV-6-infected patients. Antiviral treatment strategies were reviewed.Among 366 adult allo-HSCT recipients, 75 HHV-6 infections occurred. Three (4%) recipients were ciHHV-6. HHV-6 infections were associated with CMV (p = 0.05; sdHR 1.73, CI 0.99-3.02) and/or BKV infections (p < 0.0001; sdHR 4.63, CI 2.04-10.53) but not EBV reactivation (p = 0.34). A slower CD8+ T-cells recovery was observed until 6 months after allo-HSCT in the HHV-6-infected group (p < 0.001), independently of acute and/or chronic graft-versus-host disease. The overall probability of survival after allo-HSCT was diminished for active HHV-6-infected patients (p = 0.0326). Cord blood unit recipients had a higher risk of developing HHV-6 infection compared to bone marrow recipients (p = 0.0007; sdHR 3.82, CI 1.76-8.27). Anti-HHV-6 treatment achieved complete response in only 2/3 of the cases.In this series of allo-HSCT recipients, 4% were ciHHV-6, active HHV-6 infection was likely associated with CMV and BKV co-reactivations, delayed CD8+ T-cell recovery and poorer outcome.
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