58 vs 814 years, respectively; P=0037) than the 14 patients wi

58 vs. 8.14 years, respectively; P=0.037) than the 14 patients with no anti-VZV

avidity maturation. In healthy children, we observed no correlation between anti-VZV IgG level and AI: some children maintained low levels of high-avidity antibodies, indicating successful avidity maturation. selleck inhibitor In contrast, a significant correlation between anti-VZV IgG level and AI was present in HIV-infected children (P=0.001): anti-VZV IgG levels were significantly lower in children with a lower AI, i.e. no evidence of successful memory B-cell maturation/reactivation. Thus, the waning of anti-VZV antibodies in a significant proportion of HIV-infected children resulted from the failure to maintain and/or reactivate anti-VZV memory responses. This study showed that the waning of anti-VZV antibodies in HIV-infected Pifithrin-�� nmr children, compared with HIV-infected adults and healthy children, was associated with lower antibody avidity, reflecting the failure to generate, maintain or reactivate memory B-cell responses. Rapid antibody decline was previously reported following immunization of HIV-infected patients [1]. This may also affect humoral responses elicited by natural infection and results in absent or low antibody levels [24]. The lower anti-VZV

IgG levels were not explained by differences in age, gender, or ethnicity. A lower exposure rate to chickenpox is unlikely, as chickenpox is endemic, and HIV-infected patients have regular peer contact. HIV-infected children had higher CD4 T-cell counts than HIV-infected adults, as expected [25]. The HIV RNA level was higher in children

than in adults, because of lower HAART rates (88% vs. 99%) and suboptimally controlled infection [26,27]. Yet, HIV-infected children were almost PIK-5 18 times more likely than adults to lose anti-VZV antibodies. Our longitudinal analysis indicated that high HIV RNA level, absence of HAART and low CD4 percentage were associated with the waning of VZV-specific antibodies. Lower anti-VZV IgG levels were not attributable to a universally accelerated antibody loss: HIV-infected children had lower levels than adults throughout the 10-year study period and their antibody levels even increased slightly over time. These lower levels could reflect impaired primary responses [1,24]. However, anti-VZV IgG levels were lower in VZV-positive, HIV-infected children than in healthy children in all age quartiles except the youngest: this suggests that primary responses to VZV exposure were only impaired in older children, possibly as a result of HIV disease progression, and/or that some HIV-infected children failed to maintain/reactivate anti-VZV immunity. To define whether the failure to reactivate anti-VZV memory responses may explain the lower anti-VZV IgG levels, we compared anti-VZV IgG levels in HIV-infected and healthy children.

Leave a Reply

Your email address will not be published. Required fields are marked *

*

You may use these HTML tags and attributes: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong>