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Preprints

Assessment of hepatitis B surface antibody in children after allogeneic peripheral blood stem cell transplantation and impact of donor/recipient immunity on hepatitis B surface antibody disappearance

Yuan Q, Zhou F, Zhang H, Wang J, Zhang A, Cao Q, Chen W, Fei Y, Luo C, Gao Y.
Preprint from
Authorea Preprints
30 March 2022
PPR
PPR475698
Abstract
After allogeneic peripheral blood stem cell transplantation (PBSCT), children are at high risk of hepatitis B virus (HBV) infection because of the potential loss of HBV immunity. The factors which can affect it are not fully understand. This study aimed to assess the probability of hepatitis B surface antibody (HBsAb) disappearance after PBSCT and to evaluate the impact of donor and recipient immunity on HBsAb disappearance. A total of 110 patients who underwent PBSCT between January 2016 and December 2018 and their paired donors were retrospectively enrolled in this study. Before transplantation, 87 (79.1%) patients were HBsAb seropositive, and 23 (20.9%) were HBsAb seronegative. Fifty-five (63.2%) patients with protective HBsAb titers before PBSCT lost their HBV immunity within one year after transplantation. Univariate analysis showed that the low recipient pretransplant HBsAb titer, antithymocyte globulin (ATG) administration, corticosteroid administration and graft-versus-host disease (GVHD) were significant risk factors for HBsAb disappearance (P<0.05). Multivariate analysis showed that only recipient pretransplant HBsAb titers lower than 207.5 IU/L (P=0.022, hazard ratio (HR): 1.925, 95% confidence interval (CI): 1.101-3.367) and the presence of GVHD (P=0.033, HR=1.921, 95% CI: 1.056-3.495) were risk factors for HBsAb disappearance one year after HSCT. In conclusion, most recipients lost previously acquired immunity to HBV after PBSCT. A high titer of HBsAb in the recipient before transplantation had a protective effect against posttransplant HBsAb disappearance, but the presence of donor immunity did not significantly influence the maintenance of recipient immunity to HBV.