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Published on: September 6, 2019
Immune development in HIV-exposed uninfected children born to HIV-infected women
Maristela Miyamoto1, Aída F T B Gouvêa1, Erika Ono1
1Universidade Federal de São Paulo, Departamento de Pediatria, São Paulo, São Paulo, Brazil.
Insights
HIV-exposed uninfected children show subtle, transient immune differences compared to controls. These immune system variations in HEU individuals are mostly comparable to the general population, but their clinical impact remains unclear.
Area of Science:
- Immunology
- Pediatrics
- Infectious Diseases
Background:
- HIV-exposed uninfected (HEU) children may exhibit immune dysfunction.
- The persistence of these immune differences in HEU individuals is not well understood.
Purpose of the Study:
- To evaluate the immunological development in HEU children compared to HIV-unexposed controls.
- To determine if immune differences in HEU individuals are persistent or transitory.
Main Methods:
- Longitudinal study of HEU and control children at birth, 12 months, and 6-12 years.
- Assessed plasma levels of LPS, sCD14, cytokines, and T-cell receptor excision circles (TREC).
- Performed lymphocyte immunophenotyping to analyze immune cell populations and activation markers.
Main Results:
- HEU and controls had similar LPS levels and TREC counts at birth.
- Most cytokine levels increased from birth to 12 months and decreased by 6-12 years in both groups.
- Higher immune activation (CD38+HLA-DR+ T cells) observed in HEU at 12 months and 6-12 years; lower MIP-1β at 12 months and higher IL-4 at 6-12 years in HEU compared to controls.
Conclusions:
- The immune system development in HEU individuals is largely comparable to HIV-unexposed controls.
- Subtle, potentially transient immune differences exist in HEU children.
- The clinical significance of these immune variations in HEU individuals requires further investigation.
Abstract:
Immunological and clinical findings suggestive of some immune dysfunction have been reported among HIV-exposed uninfected (HEU) children and adolescents. Whether these defects are persistent or transitory is still unknown. HEU pediatric population at birth, 12 months, 6-12 years were evaluated in comparison to healthy age-matched HIV-unexposed controls. Plasma levels of LPS, sCD14, cytokines, lymphocyte immunophenotyping and T-cell receptor excision circles (TREC) were assessed. HEU and controls had similar LPS levels, which remained low from birth to 6-12 years; for plasma sCD14, IL-2, IL-6, IL-7, IL-10, IL-12p70, IL-13, IL-17, IFN-γ, TNF-α, G-CSF, GM-CSF and MCP-1, which increased from birth to 12 months and then decreased at 6-12 years; and for TREC/106 PBMC at birth in HEU and controls. By contrast, plasma MIP-1β levels were lower in HEU than in controls (p=0.009) at 12 months, and IL-4 levels were higher in HEU than controls (p=0.04) at 6-12 years. Immune activation was higher in HEU at 12 months and at 6-12 years than controls based on frequencies of CD38+HLA-DR+CD8+T cells (p=0.05) and of CD38+HLA-DR+CD4+T cells (p=0.006). Resting memory and activated mature B cells increased from birth to 6-12 years in both groups. The development of the immune system in vertically HEU individuals is comparable to the general population in most parameters, but subtle or transient differences exist. Their role in influencing clinical incidences in HEU is unknown.
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