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Currently
the Department studies the immunological aspects of
atherosclerosis, in particular, the sources of
development of autoimmune responses to normal components
of human blood serum.
The study of C-reactive protein has also shown that it can neutralize some haemolytic toxins of bacterial origin and decrease toxic side effects of antimycotic antibiotics. At present the molecular basis of this phenomenon is studied for its possible employment in constructing new antitoxic preparations. The investigations supervised by professor P. G. Nazarov are devoted to the immunology of the acute phase of inflammation, the acute inflammation phase proteins in particular: pentraxins (C-reactive protein, serum P component of amyloid, serum amyloid A, antiproteases alpha2 -macroglobulin and alpha1-antitripsin, complement proteins). Under investigation is the role of petraxins and other proteins of the acute phase of inflammation in immunoregulation and in immunopathology of atherosclerosis. Investigation of pentraxins in the laboratory of general immunology resulted in detection and characterization of new ligands of CRP, including the exogenous and endogenous biologically active macromolecules. These investigations have shown that pentraxins play a protective antitoxic role at the early stages of infection, until the antibodies appear. The interaction of C-reactive protein with cytokines and its influence on the cytokine regulation of immunological reactions were studied. The pentraxins were proved to make a new class of inhibitors of cytokines. The experimental data obtained show that C-reactive protein may be considered as an atherogenic factor and point to one of immunopathological mechanisms of the development of atherosclerosis. These data suggest a potential atherogenic danger of the elevation of the C-reactive protein level during inflammation episodes. It has been recently shown that acetylcholine is also a
pentraxin ligand. Their interaction is followed by weakening cardiotropic
effects of acetylcholine. |