ABSTRACT
A possibility of rising the antitumor activity of natural killers using various doses of the immunomodulator cycloferon was evaluated. A direct correlation has been revealed between the killer activity and the cycloferon dose. However, on a decrease in cycloferon concentrations by several orders, as compared with commonly accepted doses, this correlation changed for inverse. A possible mechanism of this effect is discussed in addition to practical significance of the obtained results.
Subject(s)
Acridines/pharmacology , Adjuvants, Immunologic/pharmacology , Killer Cells, Natural/drug effects , Animals , Cytotoxicity, Immunologic/drug effects , Dose-Response Relationship, Drug , Humans , K562 Cells , Killer Cells, Natural/immunology , MiceABSTRACT
Essential changes in the mononuclear glycocalix structure and function and a reduction of the blood natural cytotoxicity have been detected in children suffering from neurodermatitis. These shifts depended on the disease pattern and did not recover in clinical remission.
Subject(s)
Cytotoxicity, Immunologic/immunology , Leukocytes, Mononuclear/immunology , Neurodermatitis/immunology , Adolescent , Agglutination Tests , Child , Cytotoxicity Tests, Immunologic , Glycoproteins/immunology , Humans , Polysaccharides/immunology , Recurrence , Surface PropertiesABSTRACT
Structural changes in the blood mononuclear glycocalyx has been revealed in children suffering from neurodermatitis. These shifts correlated with the cellular ability to respond to mitogenic stimulation. Treatment by UV-irradiated blood autotransfusions normalized the structure and function of mononuclears whereas routine therapy has been ineffective.
Subject(s)
Blood Transfusion, Autologous , Blood/radiation effects , Leukocytes, Mononuclear/pathology , Neurodermatitis/therapy , Ultraviolet Rays , Adolescent , Child , Humans , Neurodermatitis/pathologyABSTRACT
In children suffering from chronic dermatoses (psoriasis and neurodermatitis), the glycocalix of blood mononuclears displays an Alcian blue dye sorption by 23-25% less than that in healthy children. The UV irradiation of their blood (254 nm), in addition to a course of UV-irradiated blood autotransfusion, resulted in an elevated sorption capacity of the mononuclear glycocalix up to the normal. A possible involvement of these changes in immunocompetent cell glycocalix in the pathogenesis of chronic dermatoses is discussed, as well as the significance of glycocalix normalization in the medicinal effect of UV-irradiated blood autotransfusion.