Persistent immunological repercussions of late antiretroviral initiation in children with HIV.

OBJECTIVE

We aimed to evaluate how age at antiretroviral treatment (ART) initiation modified immune parameters and vaccine responses in a Brazilian cohort of children with perinatally acquired HIV on long-term treatment.

DESIGN

Cross-sectional study including children <18 years; ART for ≥6 months; and HIV viral load <50 copies/ml.

METHODS

Data was abstracted from medical charts and blood was collected for serology and PBMC isolation. Antibody titers for hepatitis A and B, rubella, mumps and measles were measured. T cells with markers for senescence (CD57 + ), anergy (CD28 - ), apoptosis (CD95 + ), activation (CD38 + , CCR5 + , HLA-DR + ) and exhaustion (PD-1 + ) were analyzed by flow cytometry. Children were categorized in four groups: ART initiation <6 months; ≥6 months <1 year; ≥1 year <5 years; ≥5 years.

RESULTS

Fifty-five participants with a median age of 12 (8.3;15.9) years and median time on ART of 9 (5.0;13.2) years were included. Median age at ART initiation was 1.8 (0.6;3.6) years. Compared to those starting ART later, children who initiated ART earlier (<1 year of age, and especially < 6 months) had higher CD4 + counts, CD4 + nadir, and CD4 + /CD8 + ratio. Earlier ART was associated with CD4 + and CD8 + profiles with lower frequencies of activation, senescence, and exhaustion markers, and higher antibody titers for mumps, measles and rubella. Activation, senescence, and exhaustion markers correlated with poorer vaccine response.

CONCLUSION

Children who started ART later in life presented with worse immune outcomes even after long-term ART.