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Generation of Immature, Mature and Tolerogenic Dendritic Cells with Differing Metabolic Phenotypes
Published on: June 22, 2016
Age-matched dendritic cell subpopulations reference values in childhood.
1Department of Pediatrics, Johann Wolfgang Goethe-University Hospital, Frankfurt am Main, Germany. annekathrin.heinze@kgu.de
Scandinavian Journal of Immunology
|January 10, 2013
Summary
This study establishes age-based reference ranges for dendritic cell (DC) subpopulations in 100 healthy children using a single-platform method. Findings reveal a decline in myeloid and plasmacytoid DCs with age and lower myeloid DC counts in girls versus boys.
Area of Science:
- Immunology
- Pediatric immunology
- Cellular immunology
Background:
- Dendritic cells (DCs) are crucial antigen-presenting cells linking innate and adaptive immunity.
- Limited age-based reference values for pediatric DC subpopulations exist, hindering clinical interpretation.
- Previous studies often used dual-platform approaches, unlike the single-platform method employed here.
Purpose of the Study:
- To establish comprehensive age-matched reference ranges for myeloid DCs (mDCs) and plasmacytoid DCs (pDCs) in healthy children.
- To investigate the impact of age and sex on DC subpopulations in a larger pediatric cohort.
- To provide a reliable basis for diagnosing DC-related abnormalities in pediatric diseases and therapies.
Main Methods:
- A single-platform, lyse no-wash procedure was utilized for DC analysis.
- DC subpopulations were identified as myeloid DCs (mDCs) and plasmacytoid DCs (pDCs) based on specific cell surface markers.
- Semi-parametric regression analysis was applied to establish age-matched reference ranges for DC counts in peripheral blood.
Main Results:
- Significant age-related declines were observed in the medians of both mDCs and pDCs per μl of peripheral blood.
- Reference ranges (50%, 90%, 95%) for DC subpopulations also showed a significant decrease with increasing age.
- Absolute mDC counts per μl of peripheral blood were significantly lower in girls compared to boys across all age groups.
Conclusions:
- This study provides precise, age-matched reference ranges for pediatric DC subpopulations using a modern single-platform approach.
- The findings highlight significant developmental trends in DC counts during childhood, influenced by both age and sex.
- These established ranges are vital for identifying aberrant DC levels in pediatric conditions and post-transplant monitoring.

