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Published on: December 3, 2019
HIV-1 infection in children: a clinical and immunologic overview
1Paediatric Infectious Diseases Unit, 5th Floor Lanesborough Wing, St George's Hospital, Blackshaw Rd, Tooting, London SW 17 0QT, UK. ranachakraborty@hotmail.com
Insights
Pediatric Human Immunodeficiency Virus type 1 (HIV-1) infection, often acquired through mother-to-child transmission, leads to rapid disease progression and increased child mortality. Understanding transmission and immune responses is crucial for better pediatric HIV-1 outcomes.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Virology
Background:
- Heterosexual transmission is the primary route of Human Immunodeficiency Virus type 1 (HIV-1) infection globally, with women of childbearing age disproportionately affected.
- Vertical transmission poses a significant risk for infants, leading to severe outcomes in regions like Africa, where untreated HIV-1 infection results in high child mortality.
- Pediatric HIV-1 infection exhibits a more rapid disease progression compared to adults, with survival significantly shorter for those infected perinatally or in infancy.
Purpose of the Study:
- To review the clinical and biological factors influencing mother-to-child transmission of HIV-1.
- To explore the determinants of accelerated disease progression in HIV-1-infected infants and children.
- To summarize current knowledge on T cell depletion mechanisms and host immune responses (innate and adaptive) in pediatric HIV-1 infection.
Main Methods:
- Literature review of clinical and biological determinants of mother-to-child HIV-1 transmission.
- Summary of mechanisms underlying T cell depletion in pediatric HIV-1.
- Description of the host immune response to HIV-1 in the context of pediatric infection.
Main Results:
- Factors such as immunological immaturity, thymic destruction during active thymopoiesis, and HLA class I sharing between mother and infant may contribute to faster disease progression in children.
- Significant increase in child mortality (35-50% overall, >100% in high seroprevalence areas) is observed in regions with high rates of untreated pediatric HIV-1.
- Heterogeneity in clinical course is a characteristic of HIV-1 infection, with notably shorter survival times in children compared to adults.
Conclusions:
- Further research is needed to fully understand the factors driving rapid disease progression in pediatric HIV-1 infection.
- Elucidating the mechanisms of T cell depletion and host immune responses is critical for developing effective interventions for children.
- Addressing mother-to-child transmission and improving treatment strategies are essential to reduce the burden of pediatric HIV-1 globally.
Abstract:
Globally, HIV-1 is most often transmitted heterosexually so that nearly half of all infected adults are women of child-bearing age. Infants may acquire infection from vertical transmission. Without treatment most HIV-1 infected children in Africa die before their third birthday; as a result child mortality has increased overall by 35-50%, and by greater than 100% in areas of high seroprevalence. HIV-1 infection has a heterogeneous spectrum of clinical course. Compared to HIV-1-infected adults, survival times are considerably shorter for children who acquire the virus perinatally or during infancy. Factors contributing to accelerated disease progression in infants and children are poorly understood but may include relative immunological immaturity, thymic HIV-1-mediated destruction at a time of active thymopoiesis, and HLA class I sharing between mother and infant. This review will initially discuss clinical and biological determinants of mother-to-child transmission and disease progression in HIV-infected infants and children. Our current knowledge of the mechanisms of T cell depletion is summarised and the host immune response to HIV-1 (innate and adaptive) described in the context of Pediatric HIV-1 infection.
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