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Updated: Jul 8, 2026

New Tools to Expand Regulatory T Cells from HIV-1-infected Individuals
Published on: May 30, 2013
Learned young: HIV-1 germline-targeting vaccination in infants
Rogier W Sanders1,2,3, Tom G Caniels2, John P Moore1
1Department of Microbiology and Immunology, Weill Cornell Medicine, New York, New York, USA.
Insights
Vaccinating young children against HIV-1 may be beneficial, as their developing immune systems can produce broadly neutralizing antibodies (bNAbs). Strategies involve targeted immunogens for passive and active immunization in infants.
Area of Science:
- Immunology
- Virology
- Pediatrics
Background:
- Infants are routinely vaccinated against common viral infections.
- While HIV-1 risk is low in early childhood, immunological factors suggest potential benefits of early vaccination.
- The infant immune system may be uniquely suited for developing broadly neutralizing antibodies (bNAbs).
Purpose of the Study:
- To explore the potential benefits of vaccinating young children against HIV-1.
- To investigate strategies for inducing broadly neutralizing antibodies (bNAbs) in infants.
- To assess the role of bNAbs in infant protection against HIV-1.
Main Methods:
- Analyzing studies of HIV-1-infected individuals to understand immune system development.
- Exploring methods to target germline B cell precursors in infants for bNAb maturation.
- Designing specific envelope glycoprotein immunogens for vaccination strategies.
Main Results:
- Infant immune systems may more readily generate B cells producing broadly neutralizing antibodies (bNAbs) compared to adults.
- Sequential antigenic stimuli can guide B cell precursors to mature into bNAb-producing plasma cells.
- Multidose immunization is a standard practice in childhood vaccination frameworks.
Conclusions:
- Strategies using designed envelope glycoprotein immunogens can induce bNAbs in infants.
- Broadly neutralizing antibodies (bNAbs) can be utilized for passive protection of infants.
- Combining passive protection with active vaccination offers a potential dual approach for infant HIV-1 prevention.
Purpose Of Review:
It is standard practice to protect infants against viruses that they are exposed to early in life, during childhood, or as adults. While HIV-1 is only rarely a risk in the period between the end of breast-feeding and the onset of sexual maturity, there are good immunological and practical arguments for assessing whether vaccination of young children might be beneficial.
Recent Findings:
Studies of HIV-1-infected individuals suggest that the characteristics of the developing immune system may favor the evolution of B cells that produce broadly neutralizing antibodies (bNAbs), when compared to the same processes in adults. One way to exploit these properties of the infant immune system is targeting the germline precursors of B cells that can, over time and with the right sequential antigenic stimuli, mature into bNAb-producing plasma cells. Multidose immunization over time is standard practice within global childhood vaccine frameworks.
Summary:
We discuss strategies to accomplish the goal of inducing bNAbs, based on the use of specifically designed envelope glycoprotein immunogens. We also summarize how bNAbs may be used for passive protection of infants and combined with active vaccination.
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