This is likely to result from impaired immune responses, as reflected in a higher rate of vaccine failure to most immunizations [1]. Before highly active antiretroviral therapy (HAART) was available, chickenpox recurred frequently [2–4], and HIV-infected patients were more likely to have bacterial superinfections, pneumonia, cerebellitis and encephalitis following VZV infection [5,6]. More recently, Bekker et al. [7] reported the frequent loss of antibodies elicited by wild-type infections or immunizations in HAART-treated children. Similarly, several HIV-infected children of the Swiss Mother & Child Nutlin-3a cost HIV (MoCHiV) cohort had undetectable anti-VZV immunoglobulin

G (IgG) levels despite previously confirmed VZV infection. This observation is intriguing: the persistence

Ixazomib purchase of VZV humoral immunity is generally life-long [8], as community re-exposure and endogenous viral reactivation both contribute to reactivate anti-VZV memory responses and maintain humoral immunity [9]. This suggests limitations in the capacity of HIV-infected children to generate, maintain and/or reactivate immune memory. In Switzerland, where VZV immunization is only recommended for nonimmune adolescents, VZV is endemic and seroprevalence reaches 95% before 15 years of age [10]. Until 2008, a single dose of VZV vaccine was recommended; since then, two doses have been recommended [11]. For HIV-infected children with normal CD4 cell counts, even before adolescence,

immunization with VZV vaccine is recommended. However, this recommendation is mostly ignored. To determine whether the waning of anti-VZV antibodies in HIV-infected children resulted from impaired primary responses, accelerated antibody loss and/or failure to reactivate anti-VZV memory responses, we assessed anti-VZV IgG antibodies in sera prospectively collected over a 10-year period in HIV-infected children, compared with HIV-infected adults and age-matched noninfected healthy children. We also assessed the kinetics of anti-VZV antibodies over time, and measured their avidity, a useful marker of antigen-specific memory B cell maturation [12]. Blood samples from HIV-1-infected children were prospectively collected on a yearly basis between 1997 and 2008. All HIV-infected children Bupivacaine of the Swiss MoCHiV cohort, in which almost all HIV-infected children in Switzerland are followed, were enrolled through six referral centres. Inclusion criteria were being HIV-positive, belonging to the MoCHiV cohort, and having at least two frozen serum samples ≥1 year apart. Exclusion criteria included age <1 year to avoid misinterpretation as a consequence of the presence of maternal antibodies, and serum samples drawn within 12 months of the administration of intravenous immunoglobulins. HIV-1-infected adults were enrolled in one centre.