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ObjectivesAntibody function has been extensively studied in HIV-infected adults but is relatively understudied in children. Emerging data suggests enhanced development of broadly neutralizing antibodies (bNAbs) in children but Fc effector functions in this group are less well defined. Here, we profiled overall antibody function in HIV-infected children.DesignPlasma samples from a cross-sectional study of 50 antiretroviral therapy-naive children (aged 1-11 years) vertically infected with HIV-1 clade A were screened for HIV-specific binding antibody levels and neutralizing and Fc-mediated functions.MethodsNeutralization breadth was determined against a globally representative panel of 12 viruses. HIV-specific antibody levels were determined using a multiplex assay. Fc-mediated antibody functions measured were antibody-dependent: cellular phagocytosis (ADCP); neutrophil phagocytosis (ADNP); complement deposition (ADCD) and natural killer function (ADNK).ResultsAll children had HIV gp120-specific antibodies, largely of the IgG1 subtype. Fifty-four percent of the children exhibited more than 50% neutralization breadth, with older children showing significantly broader neutralization activity. Apart from ADCC, observed only in 16% children, other Fc-mediated functions were common (>58% children). Neutralization breadth correlated with Fc-mediated functions suggesting shared determinants of enhanced antibody function exist.ConclusionsThese results are consistent with previous observations that children may develop high levels of neutralization breadth. Furthermore, the striking association between neutralization breadth and Fc effector function suggests that HIV vaccination in children could yield multifunctional antibodies. Paediatric populations may therefore provide an ideal window of opportunity for HIV vaccination strategies.

Original publication

DOI

10.1097/qad.0000000000002976

Type

Journal

AIDS (London, England)

Publication Date

10/2021

Volume

35

Pages

1895 - 1905

Addresses

KEMRI Wellcome Trust Research Programme, Kilifi, Kenya.

Keywords

Humans, HIV-1, HIV Infections, Homeodomain Proteins, Nerve Tissue Proteins, HIV Antibodies, Vaccination, Cross-Sectional Studies, Antibody-Dependent Cell Cytotoxicity, Child, Child, Preschool, Infant, Antibodies, Neutralizing