Method of treating staphylococcus aureus infection
A staphylococcus, golden technology, applied in the direction of chemical instruments and methods, antibacterial drugs, pharmaceutical formulations, etc.
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example 1
[0082] Specific IGIV prevents MRSA S. aureus infection in mice
[0083] Hyperimmune-specific IGIV (AltaStaph TM ) ability to protect against Staphylococcus aureus infection. 15 mice were treated with AltaStaph TMimmunity. Alta Staph TM The dose contained 400 μg of specific antibody (9.6 mg total IgG / mouse). As a control, another group of 15 mice received 9.6 mg of muco-exopolysaccharide (MEP) IGIV containing approximately 15 μg of type 5-specific IgG. Low level amounts of type 5 specific IgG were about the same as seen in standard "non-specific" IGIV from commercial sources. Group 3 mice received 0.5 ml buffered saline. In addition, all mice received 0.5 ml of saline intraperitoneally 24 hours before challenge. It was demonstrated that this pre-challenge treatment of bacteria reduces mortality after challenge by bacterial exposure.
[0084] 2 x 10 in 5% mucin with three different 5 Colony forming units (CFU) of Staphylococcus aureus were challenged intraperitoneally...
example 2
[0088] Treatment of S. aureus bacteremia in humans using specific IGIV
[0089] In designed to evaluate AltaStaph TM The safety and use of hyperimmune specificity was studied in a double-blind placebo-controlled randomized trial in 40 patients with persistent S. aureus bloodstream infection (bacteremia) measuring S. aureus-specific antibody levels. IGIV for Staphylococcus aureus infection. Patients were randomly assigned to receive two doses of AltaStaph TM Or saline placebo administered intravenously in combination with standard of care treatment including treatment with antibiotics. The results of the study confirm that AltaStaph TM It was well tolerated and no drug-related serious adverse outcomes were reported. Via AltaStaph TM Treated patients were able to maintain antibody titers at protection from Staphylococcus aureus infection previously estimated by Shinefield et al. N.ENG.J.Med. 14:491-96 (2002) in patients with end-stage renal disease (ESRD) on and above sa...
example 3
[0111] Production of monoclonal antibodies against Staphylococcus aureus 336
[0112] A. Generation of immune splenocytes
[0113] S. aureus 336 polysaccharide antigen (native O-acetylated form or modified de-O-acetylated form) conjugated to recombinant extracellular protein A (S. aureus 336-rEPA) in combination with Freund's adjuvant (Freund' sadjuvants) immunized groups of 3 BALB / c female mice. Spleen cells were collected as a pool from mice that had been immunized three times at intervals of 2 weeks, and blood was drawn every other week for testing serum antibody titers. Splenocytes were prepared in 3 aliquots which were used immediately for fusion experiments or stored in liquid nitrogen for future fusion.
[0114] B. Generation of hybridomas
[0115] Fusion experiments were performed according to the procedure of Stewart and Fuller, J. Immunol. Methods 123:45-53 (1989). Supernatants from wells with growing hybrids were screened for monoclonal antibody (MAb) secretor...
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