[HTML][HTML] Loss of HIV-specific memory B-cells as a potential mechanism for the dysfunction of the humoral immune response against HIV

BM Bussmann, S Reiche, B Bieniek, I Krznaric… - Virology, 2010 - Elsevier
BM Bussmann, S Reiche, B Bieniek, I Krznaric, F Ackermann, C Jassoy
Virology, 2010Elsevier
A central, yet unresolved issue in the pathogenesis of HIV disease is the mechanism of
antibody perturbation. In this study, HIV-specific memory B-cells were quantified in groups of
infected subjects and compared with memory responses to other antigens and antibody
titers. HIV-specific memory B-cell responses were vigorous in individuals with CD4+ T-cell
counts> 350/μl and weak or undetectable in subjects with CD4+ T-cell numbers< 200/μl.
Memory B-cell loss was permanent, because antiretroviral therapy failed to restore HIV …
A central, yet unresolved issue in the pathogenesis of HIV disease is the mechanism of antibody perturbation. In this study, HIV-specific memory B-cells were quantified in groups of infected subjects and compared with memory responses to other antigens and antibody titers. HIV-specific memory B-cell responses were vigorous in individuals with CD4+ T-cell counts >350/μl and weak or undetectable in subjects with CD4+ T-cell numbers <200/μl. Memory B-cell loss was permanent, because antiretroviral therapy failed to restore HIV-specific memory responses while influenza- and tetanus toxoid-specific memory B-cells remained unaffected or recovered. Antibody titers to Gag strongly correlated with memory B-cell frequencies. In contrast, Env-specific antibodies were maintained in advanced disease despite low or undetectable levels of memory B-cells. These results provide a potential mechanism by which destruction of HIV-specific CD4+ T-cells affects the humoral immune response against HIV and compromises the ability to maintain an effective antibody response.
Elsevier