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Updated: Sep 27, 2026

Mapping Infant Immunity with Minimal Input: Integrative Single-Cell and Multiomic Profiling
Published on: April 3, 2026
Longitudinal follow-up of lymphocyte subsets during the first year of life
Po-Nien Tsao1, Bor-Luen Chiang, Yao-Hsu Yang
1Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Insights
This study tracked infant lymphocyte subsets using flow cytometry. Key findings show significant increases in T, B, and NK cells during the first year of life, establishing infant immune development reference ranges.
Area of Science:
- Immunology
- Pediatrics
- Developmental Biology
Background:
- Infant immune system development is critical for lifelong health.
- Understanding lymphocyte subset dynamics during infancy is essential for assessing immune function.
Purpose of the Study:
- To longitudinally evaluate changes in lymphocyte subpopulations in healthy infants.
- To establish reference ranges for lymphocyte subsets during the first year of life.
Main Methods:
- Longitudinal study design.
- Flow cytometric immunophenotyping of peripheral blood samples.
- Analysis of lymphocyte subsets (CD3+, CD4+, CD8+, CD19+, NK cells) at multiple time points from birth to 11 months.
Main Results:
- Absolute counts of CD3+, CD3+/CD4+ T lymphocytes increased from birth to 3 months, then stabilized.
- Absolute counts of CD3+/CD8+ T lymphocytes increased from birth to 11 months.
- Absolute counts of CD19+ B lymphocytes and NK cells showed rapid increases by 3 months and continued to rise throughout infancy.
- Relative and absolute lymphocyte subset changes did not always correlate.
Conclusions:
- Significant age-related changes occur in lymphocyte subpopulations during infancy.
- Established reference ranges provide a benchmark for infant immune development.
- Findings are crucial for clinical assessment of infant immune status.
Abstract:
A longitudinal study of lymphocyte subsets during infancy was evaluated by using the flow cytometric immunophenotyping method. Two hundred and thirteen blood samples were obtained from 92 healthy, full-term infants of the following ages: 1-7 days old (n = 43), 3 months old (n = 55), 6 months old (n = 57) and 11 months old (n = 58). The absolute numbers of CD3+ and CD3+/CD4+ T lymphocytes increased from birth to 3 months of age, and remained stable thereafter. The absolute number of CD3+/CD8+ T lymphocytes increased from birth to 11 months of age. The absolute number of CD19+ B lymphocytes and NK cells increased rapidly (3 months) after birth and continued to increase throughout the study period. However, the changes in the relative counts of lymphocyte subsets did not always correspond with the changes in their absolute numbers. These results demonstrate the age-related changes in lymphocyte subpopulations and provide reference ranges for lymphocyte subsets during infancy.
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