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Use of the TRAP protein itself as an active ingredient for the manufacture of a medicament for the treatment of Staphylococcus aureus infections

机译:TRAP蛋白本身作为活性成分在制备用于治疗金黄色葡萄球菌感染的药物中的用途

摘要

The present invention discloses the use of TRAP per se as an active ingredient for the manufacture of a medicament for the treatment of Staphylococcus aureus infection. An exogenous TRAP (native TRAP or recombinant TRAP) per se can effectively inhibit the production of Staphylococcus aureus exotoxins, thereby reducing the pathogenicity of Staphylococcus aureus. In addition, a medicament comprising TRAP also stimulates the production of corresponding antibodies in human body at the time when it is used to treat Staphylococcus aureus infections, and these antibodies can further inhibit the production of Staphylococcus aureus exotoxins. Such double actions increase the effects of medicament and provide a novel medicament action mode. Moreover, since TRAP functions merely to the toxicity of bacteria but does not affect the growth of bacteria, it cannot make bacteria readily develop drug resistance, and also effective to drug resistant Staphylococcus aureus. Moreover, no homologous sequence of the TRAP proteins of the present invention is found in human genome, so that the medicaments of TRAP cannot cause human immunologic diseases.
机译:本发明公开了TRAP本身作为活性成分在制备用于治疗金黄色葡萄球菌感染的药物中的用途。外源TRAP(天然TRAP或重组TRAP)本身可有效抑制金黄色葡萄球菌外毒素的产生,从而降低金黄色葡萄球菌的致病性。另外,包含TRAP的药物在用于治疗金黄色葡萄球菌感染时还刺激人体内相应抗体的产生,并且这些抗体可以进一步抑制金黄色葡萄球菌外毒素的产生。这种双重作用增加了药物的作用,并提供了一种新颖的药物作用方式。此外,由于TRAP仅对细菌的毒性起作用,而不影响细菌的生长,因此不能使细菌容易地产生耐药性,并且对耐药性金黄色葡萄球菌也有效。此外,在人基因组中未发现本发明的TRAP蛋白的同源序列,因此TRAP的药物不能引起人免疫疾病。

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