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Published on: September 7, 2022
Percentiles of Lymphocyte Subsets in Preterm Infants According to Gestational Age Compared to Children and
S Huenecke1, E Fryns2, B Wittekindt2
1Clinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany . sabine.huenecke@kgu.de.
Insights
Preterm infants have immature immune systems, increasing infection risk. This study establishes lymphocyte subset references for preterm infants, aiding in understanding their immune development and potential disorders.
Area of Science:
- Immunology
- Neonatology
- Pediatrics
Background:
- Preterm newborns exhibit heightened susceptibility to infections due to immature immune systems.
- Understanding immune system development in preterm infants is crucial for managing their health.
- Early immune cell profiles can indicate potential immunological challenges.
Purpose of the Study:
- To establish reference ranges for lymphocyte subsets in early preterm infants.
- To compare immune cell maturation in preterm infants during hospitalization with healthy term-born individuals.
- To provide data for assessing the immunological capability of preterm infants.
Main Methods:
- Prospective observational study involving 40 preterm infants (gestational age 26-30 weeks) and 10 term neonates.
- Peripheral blood samples analyzed using 10-colour flow cytometry for immune cell subsets.
- Development of a percentile model based on preterm infant age for lymphocyte, B cell, T cell, NK cell, T8, and T4 cell counts.
Main Results:
- Established median cell counts for T-, B-, and NK cells post-birth.
- Identified significant differences in absolute B cell counts and regulatory T cell frequencies, particularly in the earliest preterm infants (GA 26).
- Preterm infants approached the 5th to 50th percentile of lymphocyte counts by hospital discharge compared to healthy children.
Conclusions:
- This study provides the first reference percentiles for lymphocyte subsets in preterm infants.
- The data supports the interpretation of immunological status in preterm infants, aiding in the identification of immune disorders.
- These findings are valuable for clinical management and further research into preterm infant immunity.
Abstract:
Preterm newborns show an increased susceptibility to infections, conceivably related to their immature immune system. To gain further knowledge about the immune development in early preterm infants, we aimed to establish references for lymphocyte subsets and compare the maturation process during hospitalization to healthy term-born children and adolescents. For this purpose, peripheral blood samples (n = 153) were collected from 40 preterm infants, gestational age (GA) 26-30 week between 2nd and 6th day of life, and were monitored in intervals of every 2 or rather 4 weeks until the end of hospitalization. Furthermore, we analysed single sample controls of 10 term neonates. We compared these data with results of a study in healthy children and adolescent (n = 176). Flow cytometry of immune cell subsets was performed as single-platform analysis using 10-colour flow cytometry. Based on preterm's age, our percentile model allows readout of absolute cell count for lymphocytes, B cells, T cells, NK cells, T8 and T4 cells. The median (minimum) value of T-, B- and NK cells after birth was 2800 (600), 790 (120) and 140 (20) cells/μl, respectively. Major differences were found in absolute cell numbers of B cells, and in the frequency of regulatory T cells, most pronounced in the earliest preterm infants (GA 26). Compared to healthy children and adolescents, preterm infants reached lymphocyte counts in between the 5th and 50th percentile when discharging the hospital. This prospective observational study provides reference percentiles for lymphocytes subsets of preterm infants. These data are conducive to interpret immunological capability of preterm infants with possible immune disorders appropriate.
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