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Резюме. В настоящем обзоре предпринята попытка систематизировать существующие представления о наиболее значимых поверхностных антигенах иммунокомпетентных клеток и оценить их роль в процессах клеточного гомеостаза и формировании патологии.

We investigated direct effects of granulocyte-macrophage colony-stimulating factor (GM-CSF) on the surface properties and cytokine-producing activity of human monocytes/macrophages (Mc/Mphs). The CD14+cells were isolated from peripheral blood of healthy donors by positive magnetic separation. The isolated Mc/Mphs were cultured with lipopolysaccharide (LPS, 1 μg/ml) or without LPS for 24 hours. Membrane expression of CD14, CD16, CD119, CD124, and CD197 molecules was assessed by flow cytometry. The contents of tumor necrosis factor-α (TNFα), interleukin-1β (IL-1β), IL-6 and IL-10 in culture supernatants were determined by the enzyme immunoassay technique. It was found that GM-CSF at a concentration range of 0.01-10 ng/ml did significantly reduce the number of cells expressing CD197 (CC receptor of chemokine 7), without significantly affecting the percentage of CD14+(coreceptor of LPS), CD16+(low-affinity Fc receptor), CD119+(IFNγ receptor) and CD124+(IL-4 receptor) cells. At the same time, GM-CSF reduced the contents of CD197+macrophages, as well as CD14+, CD16+, and CD119+cells among the activated cell population, without significantly altering the number of CD124+cells. It was also shown that GM-CSF (10 ng/ml), was able to enhance production of TNFα and IL-6, but not IL-1β and IL-10 by activated Mc/Mphs. The results obtained indicate the ability of GM-CSF to exert both anti-inflammatory and pro-inflammatory effects upon macrophage cell populations. In general, such effects could contribute to the development of adaptive immunogenesis in peripheral tissues.