Reference Values for Extended Lymphocyte Subsets in Korean Children: A Multicenter Study Using the EuroFlow PIDOT Panel

韩国儿童扩展淋巴细胞亚群参考值:一项采用 EuroFlow PIDOT 检测的多中心研究

阅读:2

Abstract

BACKGROUND: Current reference intervals for lymphocyte subpopulations are primarily based on Western populations, with limited data available for Korean children, particularly for extended subsets. We determined absolute cell counts and percentages of lymphocyte subpopulations in Korean children, according to age and sex. METHODS: Samples from 92 children-stratified into two age groups, groups 1 (5-9 yrs) and 2 (10-17 yrs)-were obtained. Immunophenotyping was performed via flow cytometry using the Primary Immunodeficiency Orientation Tube (PIDOT) panel, primarily classifying the cells into T, B, and natural killer cell populations. T lymphocytes were divided into CD4(+), CD8(+), and CD4(-)CD8(-) subsets; T and B cells were further subdivided according to their maturation stage. RESULTS: Children in group 1 exhibited higher absolute counts of total B cells, unswitched memory B cells/plasma cells, total T cells, CD4(+) naïve cells, and TCRγδ(+) T cells than those in group 2. In contrast, Group 2 children showed higher absolute counts of CD4(+) effector memory (EM) T cells. Males had higher absolute counts of total B cells, particularly pregerminal center B cells, CD4(+) EM cells, and CD8(+) terminally differentiated T cells, whereas females showed higher proportions of CD4(+), CD4(+) naïve, and CD8(+) central memory/transitional memory T cells. CONCLUSIONS: To the best of our knowledge, this study is the first to establish reference values for extended lymphocyte subsets in Korean children using the PIDOT panel. Age, sex, and laboratory-related factors influenced lymphocyte subset distributions. These findings may serve as reference data for immune disorders and immunotherapy in pediatric populations.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。