It is found that phagocytosis in animals immunized with Pseudomonas aeruginosa, Staphylococcus aureus, and Staphylococcus epidermidis is suppressed in comparison with intact animals, and the degree of suppression rises with the antibody titer. Morphological study of the site of infection shows that antibodies markedly enhance bacteriopyknosis, i.e., convert bacteria into nonphagocytizable detritus. Focal suppression of phagocytosis in immunized animals is attributed to rapid bacteriopyknosis and, consequently, to a sharp decrease in the number of intact bacteria that can be digested by phagocytes.
Key Words: infectious immunity; antibodies; phagocytosis; nonspecific organism's resistanceEnhanced phagocytosis in immunized individuals has been considered as the main mechanism of antibacterial immunity. This enhancement is provided by antibodies [1,2,5,9]. Antibodies mediate bacterial binding to the phagocyte surface with subsequent formation of the antibody-bacterium complexes which trigger the classical pathway of complement activation. As a result, bacteria bind to phagocytes via the receptors for antibodies and complement [6,10], Opsonization, i.e., the phagocyte-stimulating effect of antibodies, was confirmed by in vitro experiments: absorption and killing of bacteria by neutrophils and macrophages is considerably increased in the presence of antibodies. Systemic administration of antibodies often produces a protective effect and alleviates the disease. The protective effect of antibodies in vivo and the opsonizing effect in vitro provide the basis for the modern concept of infectious immunity. This theory has been confirmed by considerable experimental and clinical data accumulated during the last century; however, there is evidence contradicting it. It was found that despite the pronounced opsonizing effect, antibodies elicit no protective effect in some experimental infections [7,8,11]. These reports, however, did not Here we report a simple experiment demonstrating that phagocytosis in vivo, in contrast to that in vitro, is inhibited by antibodies and make an attempt to explain this phenomenon.
MATERIALS AND METHODSExperiments were carried out on nonpedigree rats weighing 170-300 g. The animals were infected with one-day-old agar cultures of Pseudomonas aeruginosa (strain 453), Staphylococcus aureus (strains 3377 and 3384), and Staphylococcus epidermidis (strain 4017) isolated from burns. The bacteria were suspended in Hanks' solution, and 0.3 ml of this suspension was injected into the gastrocnemius muscle. The intensity of phagocytosis was assessed by the mass of exudate in the site of injection after 7 days. All necrotic detritus from the site of infection was collected and weighted. For active immunization the same cultures were injected into rats in a 10-fold lower dose 3 times at one-week intervals. Immunized and control (intact) rats were infected simultaneously with the same bacterial suspension one week after the last immunization. Some animals were sacrificed