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Differentiation of Activated Human T-Lymphocytes Under the Influence of Interleukin-8. P. 67–73

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Section: Medical and biological sciences

UDC

576.536:612.112.94:57.086.83

Authors

Maksim E. Menyaylo*, Vladimir V. Malashchenko*, Vyacheslav A. Shmarov*, Natal’ya D. Gazatova*, Ol’ga B. Melashchenko*, Egor O. Shun’kin*, Andrey G. Goncharov*
*Immanuel Kant Baltic Federal University (Kaliningrad, Russian Federation)

Abstract

Scientific papers describe in detail the role of interleukin-8 (IL-8) in the regulation of the innate immune system. However, the effect of this chemokine on the components of the adaptive immune system requires further investigation. This study aimed to evaluate the effect of IL-8 on the differentiation of activated human T-lymphocytes under the conditions of in vitro cell culture. From the whole blood of practically healthy donors we isolated mononuclear cells which were used for positive magneticactivated sorting of CD3+ cells that were then cultured in vitro with recombinant IL-8 in different concentrations (0.01; 0.10; 1.00; 10.00 ng/ml) accompanied by TCR activation. The effect of IL-8 on the subpopulation of human T-lymphocytes was assessed using flow cytometry by the changes in the number of molecules that determine the subpopulations of T-lymphocytes (CD4, CD45RA, and CD197). We found that IL-8 is able to cause differentiation of CD4+ T-lymphocytes from naïve (CD45RA+CD197+) to effector memory (CD4+CD45RA-CD197-) T-cells. Further, we identified an increase in the number of activated CD4- T-lymphocytes with the phenotype of effector memory cells against the background of decreasing number of naïve and central memory T-cells (CD45RA+CD197-). Thus, co-culturing of IL-8 and activated T-lymphocytes resulted in the transition of CD3+CD4+ and CD3+CD4- subpopulations to the later stages of differentiation. The findings indicate the involvement of IL-8 in the processes associated with maturation of activated adaptive immune system cells.

Keywords

interleukin-8, human T-lymphocyte activation, human T-lymphocyte differentiation
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