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Updated: Jun 13, 2026

Development and Functional Characterization of Murine Tolerogenic Dendritic Cells
Published on: May 18, 2018
Age-dependent changes in peripheral blood dendritic cell subsets in normal children and children with specific
Harumi Jyonouchi1, Chongwei Cui, Lee Geng
1Division of Allergy/Immunology and Infectious Diseases, Department of Pediatrics, UMDNJ-NJMS, Newark, NJ, USA. jyanouha@umdnj.edu
Insights
Plasmacytoid dendritic cell (PDC) numbers decrease with age in healthy children. Specific polysaccharide antibody deficiency (SPAD) patients show altered PDC development, highlighting the need for age-specific controls.
Area of Science:
- Immunology
- Pediatric immunology
- Cellular immunology
Background:
- Dendritic cells (DCs), including myeloid (MDC) and plasmacytoid (PDC) subsets, are key in immunity.
- Immune system development post-birth involves dynamic changes in immune cells.
- Normative data on pediatric DC subsets are lacking, hindering disease evaluation.
Purpose of the Study:
- To investigate age-associated changes in MDC and PDC subsets in healthy children.
- To analyze CD40 and CD86 expression on PDCs as maturation markers.
- To compare DC subsets in healthy children with those in children with specific polysaccharide antibody deficiency (SPAD).
Main Methods:
- Flow cytometry analysis of DC subsets (MDC1, MDC2, PDC).
- Quantification of CD40 and CD86 expression on PDCs.
- Comparison between 50 healthy children and 25 SPAD patients.
Main Results:
- PDC numbers showed a significant age-dependent decrease in healthy children (p < 0.0001).
- MDC1/MDC2 numbers did not exhibit linear age-dependent changes; MDC1/PDC ratio normalized after age 10.
- SPAD patients lacked age-associated changes and displayed reduced CD86 expression on PDCs.
Conclusions:
- DC subsets in healthy children undergo lineage-specific, age-dependent changes.
- SPAD patients may have altered DC development compared to healthy children.
- Age-appropriate normative data is crucial for pediatric immune studies.
Abstract:
Myeloid and plasmacytoid dendritic cells (MDC/PDC) play crucial roles in bridging adaptive and innate immunity by affecting development of both cellular and humoral immunity. The immune system evolves after birth as reflected in dynamic changes in numbers and functions of various immune cells with age. However, age-associated changes in DC subsets in children have not been elucidated despite the fact that such normative data are crucial for evaluating alternations of DC subsets in various pediatric diseases. This study addressed age-associated changes in DC subsets and CD40/86 expression on PDC (markers of maturation/activation) in 50 healthy children in comparison with 25 children with specific polysaccharide antibody deficiency (SPAD). Our results revealed age-dependent decrease of PDC numbers (p < 0.0001), although there was no age-associated changes in CD40/CD86 expression. MDC1/MDC2 numbers did not reveal such linear age-dependent changes and MDC1/PDC ratio reached around 2 as typically seen in young adults after 10 years of age. In contrast, SPAD patients did not reveal such age-associated changes and showed decreased fluorescence intensity of CD86 in PDC cells. These results indicate lineage specific, age-dependent changes in DC subsets in normal children and possible altered development of these cells in SPAD children, emphasizing the importance of age-appropriate controls.
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