Direct effects of interleukin-8 on growth and functional activity of T lymphocytes

Abstract

CD3⁺ T-lymphocytes were isolated from the normal donors by positive magnetic separation. Activation of the T cells with particles conjugated with antibodies to CD3, СD28 and СD2 molecules led to a marked increase in T-cell production of interleukine-8 (IL-8). We present evidence that IL-8 receptor α-chain (CXCR1, CD181) is expressed on the cell surface of 13.3% T cells. Activation of T-lymphocytes resulted in significant enhancement of CD181⁺ cells both in naive CD4⁺ T cell and terminally differentiated effector CD4⁺ T cell compartments with concomitant reduction of CD181⁺ cells in effector memory CD4⁺ T cell subset. The level of T cell activation was assessed judging from the surface expression of CD25 (IL-2 receptor α-chain). We demonstrate that IL-8 treatment (0.01-10.0ng/ml concentration range) reduced the activation status of both CD4^- and CD4⁺ effector memory T cells, as well as terminally differentiated effector T cells, without significantly affecting the activation of naive T cells or central memory T cells. In addition, IL-8 up-regulated IL-2 and down-regulated IL-10 production by activated T cells, with no effect on interferon-gamma (IFN-γ) and IL-4 production. Data obtained suggests the importance of IL-8 in the direct regulation of adaptive T cell reactivity.

Keywords: Adaptive immunity; CXCR1; Interleukin-8; T-cell subset.