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Establishing Reference Values for Peripheral Blood Lymphocyte Subsets of Healthy Children in China Using a Single
Liangjun Zhang1, Huixiu Zhong1, Bin Wei2
1Department of Laboratory Medicine, Zigong First People's Hospital, Sichuan Province, China.
Insights
Establishing age-matched reference values for lymphocyte subsets in children is crucial for immune assessment. This study provides essential pediatric reference intervals for T cells, B cells, and NK cells, aiding disease monitoring.
Area of Science:
- Immunology
- Pediatric Hematology
Background:
- Lymphocyte subset counts naturally change throughout childhood.
- Accurate, age-specific reference values are essential for diagnosing pediatric immune disorders.
Purpose of the Study:
- To establish age- and sex-specific reference intervals for lymphocyte subsets in healthy children.
- To provide a reliable basis for assessing immune status in pediatric conditions.
Main Methods:
- Analyzed peripheral blood from 813 healthy children using standardized methods (CLSI C28-A3).
- Employed statistical techniques including Box-Cox transformation and Tukey's method for data normalization and outlier removal.
- Stratified data by age groups (0-18 years) and sex to identify relevant factors.
Main Results:
- Age significantly impacts lymphocyte subset counts in children.
- Absolute counts of lymphocytes, T cells, CD4 T cells, CD8 T cells, and B cells increase in the first year and decline thereafter.
- CD4 T cells and CD4+/CD8+ ratio decrease with age, while CD8 T and DNT cells increase; NK and NKT-like cells increase and stabilize after one year.
Conclusions:
- Age-related reference intervals for lymphocyte subsets in children were successfully established.
- These reference values are vital for accurate monitoring and assessment of immune system changes in pediatric diseases.
Abstract:
Lymphocyte subsets significantly change during childhood; thus, age-matched reference values derived from healthy children are crucial. We established reference values for lymphocyte subsets, including T cells (CD3+), CD4 T cells (CD3 + CD4+), CD8 T cells (CD3 + CD8+), double negative T (DNT) cells (CD3 + CD4-CD8-), B cells (CD3-CD19+), NK cells (CD3-CD56+), and NKT-like cells (CD3 + CD56+) in the peripheral blood of 813 healthy children. We used the method of the international standard document (Clinical Laboratory Standard Institute C28-A3) to establish reference intervals with a single platform. First, we used the Skewness and Kurtosis test to analyze the normality of the data. The nonnormally distributed data was transformed into approximately normal distribution by the Box-Cox transformation. Second, we used the Tukey's method to eliminate outliers. Further, all the subjects were grouped into subgroups according to sex (male and female) and age (0-1 month, 2-12 months, 1-3 years, 4-6 years, and 7-18 years). We used the standard normal deviation test (Z-test) to evaluate whether age and sex were possible grouping factors. The analyses indicated age to be an important factor associated with changes in lymphocyte subsets. The absolute number of lymphocyte subsets and total number of lymphocytes, T cells, CD4 T cells, CD8 T cells, and B cells gradually increase from birth to 12 months and then gradually decrease with age. Furthermore, CD4 T cells and the ratio of CD4+/CD8+ gradually decrease with age. In contrast, CD8 T and DNT cells gradually increase with age. The percentage and number of NK and NKT-like cells gradually increase with age and remain stable between 1 and 18 years of age. In conclusion, the age-related reference intervals established in healthy children in this study can aid in monitoring and assessing the changes in immune levels in diseased conditions.
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