Method for nonspecific cellular immune stimulation
AssigneeAnthony G. Gristina
InventorsAnthony G. Gristina, Quentin N. Myrvik
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Abstract
A non-specific host defense cell augmentation technique for enhanced microorganism killing utilizes any phagocytosable, biocompatible particle to prime macrophages for enhanced oxidative response and bacterial killing. Patients can have the benefits of primed macrophages in one to four days, and experiments have demonstrated over a 100-fold increase in oxidative potential within this time period. The oxidative response and killing potential is non-immunospecific, meaning not one organism, not a vaccine, and broadly applicable simultaneously to bacteria and viruses as well as tumor cells. The effects have been demonstrated to have a seven day duration indicating non-tissue toxic residual effects and potential for repeated use at monthly intervals.
Claims8
A method for priming macrophages in vivo in patients in need of prophylactic treatment for bacterial and viral infections, comprising the steps of:
- day when a providing patient enhanced macrophage activity
- by administering to said patient an effective dose of phagocytosable particles selected from the group consisting of biodegradable particles, opsonized zymosan particles, PMMA latex, polystyrene, heat killed-BCG, and heat killed Staphylococcus epidermis one to four days prior to said day when said patient requires enhanced macrophage activity, whereby said phagocytosable particles prime macrophages in said patient for enhanced macrophage activity.
A method for priming macrophages in vivo in patients in need of enhanced bactericidal and virucidal activity, comprising the steps of:
- administering to a patient that has been infected with a bacterial or viral agent and would benefit from enhanced macrophage activity
- an effective dose of phagocytosable particles selected from the group consisting of biodegradable particles, opsonized zymosan, PMMA latex, polystyrene, heat killed-BCG, and heat killed Staphylococcus epidermis, whereby said phagocytosable particles prime macrophages in said patient for enhanced macrophage activity one to four days after administration.
Dependencies are inferred from the claim text.