Open Access

ARTICLE

Intracellular T-cell cytokine levels are age-dependent in healthy children and adults

Florian Hoffmann^1,*, Michael H. Albert^1,*, Stephan Arenz³, Christoph Bidlingmaier¹, Nadine Berkowicz¹, Sabine Sedlaczek¹, Holger Till², Ingo Pawlita¹, Ellen D. Renner¹, Michael Weiss⁴, Bernd H. Belohradsky¹

1 Department of Infection and Immunity, Children’s Hospital, Ludwig Maximilians-University, Lindwurmstr. 4, 80337 Munich, Germany
2 Department of Surgery, Dr. von Haunersches Kinderspital, Ludwig-Maximilians-University, Munich, Germany
3 Children’s Hospital Schwabing, Technical University of Munich, Munich, Germany
4 Children’s Hospital Amsterdamer Str, Köln, Germany

* Corresponding Author: M.H. Albert,

European Cytokine Network 2005, 16(4), 283-288.

Abstract

Intracellular detection of cytokines via fluorescent antibody staining and flow cytometry has quickly become a standard method in experimental immunology. However, in pediatrics most studies have been hampered by the exclusion of healthy control individuals or have been skewed by neglecting to observe age-dependent differences in cytokine production. We therefore intended to establish normal values for different age groups and to describe the age-dependent development of cytokine profiles. Whole blood from 46 healthy children and 33 adults was analyzed by flow cytometry after stimulation with PMA, ionomycin and Mmonensin, and staining with anti-cytokine and surface antibodies. In the pediatric population, we found a significant positive correlation between age and intracellular cytokine levels of IFN-γ, IL-2, IL-4 and TNF-α in CD4+ cells, as well as for IFN-γ and TNF-α in CD8⁺ cells. In adulthood, no such striking trend could be detected, but significant correlation was found for IL-10 in CD4⁺ cells and IFN-γ in CD8+ cells as well as for TNF-α in both cell subgroups. We present here the first systematic analysis of intracellular cytokine production in normal, healthy children between the ages of 0 to 18 years compared to results in adults. These data may provide a reference basis for the study of cytokine secretion patterns, and they also demonstrate a significant maturation of the T-cell cytokine production capacity from birth to adulthood.

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Keywords

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