期刊
JOURNAL OF INFECTIOUS DISEASES
卷 223, 期 4, 页码 709-713出版社
OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiaa422
关键词
human herpesvirus 6; HHV-6; CD4(+) T cell; hematopoietic cell transplant
资金
- National Institute of Allergy and Infectious Diseases, National Institutes of Health [T32AI118690, K23 AI119133]
- National Institutes of Health [5P50GM115305-04]
- HHV-6 Foundation (Dharam Ablashi Research Fund)
This study aimed to determine the correlation between donor-derived HHV-6B-specific CD4(+) T-cell abundance and HHV-6B detection post allogeneic hematopoietic cell transplantation. The findings suggest that donor-derived immunity plays a critical role in controlling HHV-6B reactivation among transplant recipients.
We sought to determine whether donor-derived human herpesvirus (HHV) 6B-specific CD4(+) T-cell abundance is correlated with HHV-6B detection after allogeneic hematopoietic cell transplantation. We identified 33 patients who received HLA-matched, non-T-cell-depleted, myeloablative allogeneic hematopoietic cell transplantation and underwent weekly plasma polymerase chain reaction testing for HHV-6B for 100 days thereafter. We tested donor peripheral blood mononuclear cells for HHV-6B-specific CD4(+) T cells. Patients with HHV-6B detection above the median peak viral load (200 copies/mL) received approximately 10-fold fewer donor-derived total or HHV-6B-specific CD4(+) T cells than those with peak HHV-6B detection at <= 200 copies/mL or with no HHV-6B detection. These data suggest the importance of donor-derived immunity for controlling HHV-6B reactivation.
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