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用包埋于微球中的金黄色葡萄球菌裂解物进行免疫接种。

Immunization with Staphylococcus aureus lysate incorporated into microspheres.

作者信息

O'Brien C N, Guidry A J, Douglass L W, Westhoff D C

机构信息

Immunology and Disease Resistance Laboratory, USDA, Beltsville, MD 20705, USA.

出版信息

J Dairy Sci. 2001 Aug;84(8):1791-9. doi: 10.3168/jds.S0022-0302(01)74617-6.

Abstract

Antibiotics are of limited value against Staphylococcus aureus due to development of resistant strains, scar tissue formation, and blockage of ducts due to inflammation. Though macrophages are the predominant cell type in the mammary gland, they are primarily scavenger cells and are not effective against bacteria entering the gland. Neutrophil phagocytosis is the bovine's primary defense against S. aureus mastitis. Attempts to develop vaccines that enhance neutrophil phagocytosis by stimulating production of opsonizing antibodies to S. aureus have met with limited success because of the low immunogenicity of the exopolysaccharide capsule surrounding S. aureus. Staphylococcus aureus can also adhere to and penetrate epithelial tissue. This study was conducted to determine whether lysates of S. aureus encapsulated in biodegradable microspheres would increase the production of opsonizing antibodies to capsule and block adherence. Four groups of four cows each were injected with 1 ml of the respective treatment in the area of the supramammary lymph node and 1 ml in the hip muscle. The treatments were: lysate in NaCl, lysate in Freund's incomplete adjuvant (FICA), lysate in microspheres in NaCl, and lysate in microspheres in FICA. Antigen in microspheres produced a similar antibody response to antigen emulsified in FICA, but to a lesser magnitude. Antigen in microspheres produced antibodies that were more opsonic for neutrophils at 20 and 52 wk postimmunization and inhibited S. aureus adherence to mammary epithelium. Ability to control antigen release and presentation, and the benefit of a single injection for long-term immunity using microspheres warrants additional studies.

摘要

由于耐药菌株的产生、瘢痕组织的形成以及炎症导致的导管阻塞,抗生素对金黄色葡萄球菌的作用有限。尽管巨噬细胞是乳腺中的主要细胞类型,但它们主要是清除细胞,对进入腺体的细菌无效。中性粒细胞吞噬作用是牛抵御金黄色葡萄球菌乳腺炎的主要防御机制。试图通过刺激产生针对金黄色葡萄球菌的调理抗体来增强中性粒细胞吞噬作用的疫苗研发取得的成功有限,因为围绕金黄色葡萄球菌的胞外多糖荚膜免疫原性较低。金黄色葡萄球菌还可黏附并穿透上皮组织。本研究旨在确定包裹在可生物降解微球中的金黄色葡萄球菌裂解物是否会增加针对荚膜的调理抗体的产生并阻止黏附。四组奶牛,每组四头,在乳房上淋巴结区域注射1毫升相应处理液,在臀部肌肉注射1毫升。处理方式为:氯化钠中的裂解物、弗氏不完全佐剂(FICA)中的裂解物、氯化钠中的微球裂解物以及FICA中的微球裂解物。微球中的抗原产生的抗体反应与FICA乳化的抗原相似,但程度较小。微球中的抗原产生的抗体在免疫后20周和52周时对中性粒细胞的调理作用更强,并抑制金黄色葡萄球菌对乳腺上皮的黏附。控制抗原释放和呈递的能力,以及使用微球单次注射实现长期免疫的益处值得进一步研究。

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