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Published on: September 23, 2022
Children with perinatally acquired HIV exhibit distinct immune responses to 4CMenB vaccine
Nicola Cotugno1,2, Alessia Neri1,3, Marco Sanna1
1Clinical and Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Insights
Children with perinatally acquired HIV (PHIV) show reduced immune responses to meningococcal vaccines compared to healthy children. Further research is needed to understand long-term vaccine immunity in this vulnerable population.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Children with perinatally acquired HIV (PHIV) exhibit suboptimal immune responses, necessitating tailored vaccination strategies.
- Group B meningococcal (4CMB) vaccines are crucial for preventing invasive meningococcal disease.
Purpose of the Study:
- To assess the safety and immunogenicity of a 4-component group B meningococcal vaccine in children with PHIV on antiretroviral therapy.
- To compare immune responses between children with PHIV and healthy controls (HCs).
Main Methods:
- Administered two doses of 4CMB vaccine to children with PHIV and HCs.
- Assessed antibody responses using human serum bactericidal antibody (hSBA) assay and IgG titers.
- Investigated B cell populations and gene expression via flow cytometry and real-time PCR.
Main Results:
- The vaccine demonstrated a good safety profile in both groups.
- Children with PHIV showed reduced immunogenicity compared to HCs.
- PHIV group exhibited altered B cell subset distribution and distinct gene expression patterns post-vaccination.
Conclusions:
- While 4CMB vaccination is safe and immunogenic in children with PHIV, their immune response is less robust than in HCs.
- PHIV is associated with unique immune signatures following vaccination, impacting B cell subsets.
- Long-term vaccine-induced immunity maintenance in PHIV requires further investigation.
Abstract:
Children with perinatally acquired HIV (PHIV) have special vaccination needs, as they make suboptimal immune responses. Here, we evaluated safety and immunogenicity of 2 doses of 4-component group B meningococcal vaccine in antiretroviral therapy-treated children with PHIV and healthy controls (HCs). Assessments included the standard human serum bactericidal antibody (hSBA) assay and measurement of IgG titers against capsular group B Neisseria meningitidis antigens (fHbp, NHBA, NadA). The B cell compartment and vaccine-induced antigen-specific (fHbp+) B cells were investigated by flow cytometry, and gene expression was investigated by multiplexed real-time PCR. A good safety and immunogenicity profile was shown in both groups; however, PHIV demonstrated a reduced immunogenicity compared with HCs. Additionally, PHIV showed a reduced frequency of fHbp+ and an altered B cell subset distribution, with higher fHbp+ frequency in activated memory and tissue-like memory B cells. Gene expression analyses on these cells revealed distinct mechanisms between PHIV and HC seroconverters. Overall, these data suggest that PHIV presents a diverse immune signature following vaccination. The impact of such perturbation on long-term maintenance of vaccine-induced immunity should be further evaluated in vulnerable populations, such as people with PHIV.
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