Reference values for B cell subpopulations from infancy to adulthood

B细胞 CD38 免疫学 生物 个体发育 外围设备 幼稚B细胞 细胞 记忆B细胞 淋巴细胞 T细胞 免疫系统 细胞生物学 内科学 医学 遗传学 干细胞 抗原提呈细胞 抗体 川地34
作者
Henner Morbach,Eva-Maria Eichhorn,Johannes G. Liese,Hermann Girschick
出处
期刊:Clinical and Experimental Immunology [Oxford University Press]
卷期号:162 (2): 271-279 被引量:316
标识
DOI:10.1111/j.1365-2249.2010.04206.x
摘要

The composition of the peripheral blood lymphocyte compartment underlies developmental changes during ontogeny. Recently, several new B cell populations have been characterized which were suggested to develop in an age-dependent manner. However, age-dependent reference values for distinct B cell populations have rarely been reported. Therefore, we have characterized developmental changes in peripheral B cell populations from infancy to adulthood in order to define age-dependent reference values. Using a flow cytometric approach we analysed the frequencies as well as the absolute counts of naive, switched and non-switched memory B cells, CD27-negative memory B cells, transitional B cells as well as CD21(low) CD38(low) B cells from neonates up to the age of 50 years. Most of the B cell subsets showed age-dependent developmental changes: while the peripheral B cell pool during infancy is characterized predominantly by transitional and naive B cells, the fraction of switched and non-switched memory B cells increases gradually with age. CD21(low) CD38(low) B cells as well as plasmablasts do not exhibit developmental changes. In summary, we could demonstrate particular changes in the peripheral blood B cell compartment during ontogeny. This study provides reference values of different B cell subpopulations offering comparability for studies addressing disturbed peripheral B cell development in immunodeficiency, autoimmunity or B cell reconstitution following cell-depleting therapies.

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