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Age-Dependent Normalization Functions for T Lymphocytes in Healthy Individuals
Juliane Schröter1, José A M Borghans2, W Marieke Bitter3
1Theoretical Biology and Bioinformatics, Utrecht University, Utrecht, the Netherlands.
This study models T lymphocyte (CD3+, CD3+CD4+, CD3+CD8+) counts in healthy Dutch individuals aged 0-62 years. New functions describe lymphocyte trajectories, aiding disease research and treatment monitoring.
Area of Science:
- Immunology
- Biostatistics
- Human Physiology
Background:
- Lymphocyte counts change significantly with age, particularly in children.
- Existing normalization functions are limited and often exclude pediatric data.
- Accurate reference data is crucial for understanding lymphocyte dynamics in health and disease.
Purpose of the Study:
- To develop novel normalization functions for T lymphocyte (CD3+, CD3+CD4+, CD3+CD8+) counts and percentages across a wide age range (0-62 years).
- To establish reference trajectories for lymphocyte dynamics in a healthy Dutch population.
- To provide tools for quantifying lymphocyte changes in longitudinal studies, including disease states like HIV.
Main Methods:
- Analysis of cross-sectional data from 673 healthy Dutch individuals.
- Fitting lymphocyte subset data (naive and memory T cells) using a delayed exponential function.
- Modeling absolute cell counts derived from percentages and total lymphocyte counts.
Main Results:
- A delayed exponential function accurately described T lymphocyte trajectories.
- Parameter estimates were obtained for each T cell subset, reflecting both count and percentage changes.
- T lymphocyte counts showed an increasing trend in the first six months of life.
Conclusions:
- The study provides robust functions for T lymphocyte counts and percentages in the Dutch population.
- These functions serve as essential references for studying T lymphocyte dynamics in various diseases.
- The developed models enable precise quantification of lymphocyte changes in longitudinal studies, aiding clinical insights.
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