NK cell-mediated cytotoxicity modulation by A2 adenosine receptor agonist in different mammalian species

Folia Microbiologica - Tập 54 - Trang 364-368 - 2009
M. Kuldová1, J. Svoboda1, F. Kovářů2, L. Vannucci1, H. Kovářů3, A. Fišerová1,4
1Department of Immunology and Gnotobiology, Institute of Microbiology, v.v.i., Academy of Sciences of the Czech Republic, Prague, Czech Republic
2Section of Morphology and Physiology, Veterinary and Pharmaceutical University, Brno, Czech Republic
3Department of Psychiatry, 1st Faculty of Medicine, Charles University in Prague, Prague, Czech Republic
4Laboratory of Natural Immunity, Department of Immunology and Gnotobiology, Institute of Microbiology, Academy of Sciences of the Czech Republic, Prague 4, Czech Republic

Tóm tắt

Adenosines, endogenous purine nucleosides, appear in the extracellular space under metabolically stressful conditions associated with ischemia, inflammation, and cell damage. Their activity on innate immunity is prevalently inhibitory and can develop both in infectious and neoplastic diseases. During cancer development, tumor cells that release high concentrations of adenosines can impair the function of tumor-infiltrating lymphocytes and assist tumor growth by neo-angiogenesis. We evaluated the influence of A2 adenosine receptor (A2AR) agonist on cytotoxic-cell response comparing human with other mammalian species (rodents, pigs, goats), both in healthy and in cancer conditions. The A2AR agonist developed dose-dependent inhibition of the cytotoxic activity of immune effector cells in all studied species. However, variability of the response was observed in relation to the species and the target cells that were used. Altogether, our data indicate that the A2AR plays a central role in adenosine-mediated inhibition of immune response to tumors.

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