This report deals with the effects of cyclic nucleotide derivatives and immunostimulators on phagocytosis of
Staphylococcus aureus and other opportunistic pathogens by polymorphonuclear leucocytes and macrophages.
1) Mice infected intraperitoneally with diffuse-type staphylococci showed an increase fatality when pretreated with 10mg/mouse of DBcAMP and 20ng/mouse of cholera toxin, but a slight decrease when pretreated with 0.25mg/mouse of 8-Br-cGMP.
2) When mice were pretreated intraperitoneally with 1KE of OK-432, an immunostimulant prepared from the Su strain of streptococci, none or less than 20% of them died from infection with Smith diffuse staphylococci. Pretreatment of mice with 1KE of OK-432 was more effective than pretreatment with 10 or 100μg of the heat-killed Su strain of streptococci, which corresponded to 0.1 or 1.0KE of OK-432, respectively, or with 100μg of zymosan particles.
3) Pretreatment by intravenous injection with OK-432 protected mice from intraperitoneal challenge not only with
Staphylococcus aureus but also with some other opportunistic pathogens, such as
Serratia marcescens TO-5,
Pseudomonas aeruginosa and
Candida albicans.
4) Intravenous injection with 1KE of OK-432 for 7 days prevented mice from decreasing in resistance to intraperitoneal infection with Smith diffuse staphylococci. This resistance had been developed in these mice by intraperitoneal injection with 10μg of water-soluble dexamethasone phosphate ester for 7 successive days.
5) Macrophages derived from OK-432 treated rabbits had stronger phagocytic activity
in vitro than those derived from untreated rabbits.
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