首页> 美国卫生研究院文献>Infection and Immunity >Protection of mice against the lethal toxicity of a lipopolysaccharide (LPS) by immunization with anti-idiotype antibody to a monoclonal antibody to lipid A from Eikenella corrodens LPS.
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Protection of mice against the lethal toxicity of a lipopolysaccharide (LPS) by immunization with anti-idiotype antibody to a monoclonal antibody to lipid A from Eikenella corrodens LPS.

机译:通过用抗独特型抗体针对来自埃肯氏菌的脂A的单克隆抗体的抗独特型抗体进行免疫保护小鼠免受脂多糖(LPS)的致死毒性。

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摘要

We produced anti-idiotype antibodies to antibody to lipid A from Eikenella corrodens. The ALA-1 monoclonal antibody (immunoglobulin M [IgM] isotype), which had already been produced in our laboratory (T. Kato, I. Takazoe, and K. Okuda, Infect. Immun. 57:656-659, 1989), had reacted strongly with lipid A from E. corrodens, Escherichia coli, and Salmonella minnesota. Four anti-idiotype monoclonal antibodies to ALA-1 (Ab1), designated A2LA-1 (IgG1 isotype), A2LA-2 (IgG2a isotype), A2LA-3 (IgG2a isotype), and A2LA-4 (IgG3 isotype), which recognized the idiotype Ab1, were produced. A2LA-1, A2LA-2, and A2LA-3 were capable of over 61% inhibition of ALA-1 reactivity to E. coli J5 lipid A in an enzyme-linked immunosorbent assay system. The sera of mice and rabbits immunized with the anti-idiotype antibodies revealed that the internal image anti-idiotype antibody induced the production of IgG antibodies that cross-reacted with or bound to lipid A. These studies indicate that A2LA-1 and A2LA-2 contained an antigenic epitope that mimicked lipid A. Immunization of mice with A2LA-1 resulted in prevention of lethal toxicity from E. coli J5 lipopolysaccharide.
机译:我们生产了抗艾肯氏球菌脂质A的抗独特型抗体。已经在我们实验室中生产的ALA-1单克隆抗体(免疫球蛋白M [IgM]同种型)(T。Kato,I。Takazoe和K. Okuda,Infect。Immun。57:656-659,1989),曾与大肠杆菌,脂质体和明尼苏达沙门氏菌的脂质A强烈反应。四种针对ALA-1(Ab1)的抗独特型单克隆抗体,分别命名为A2LA-1(IgG1同种型),A2LA-2(IgG2a同种型),A2LA-3(IgG2a同种型)和A2LA-4(IgG3同种型)产生了独特型Ab1。在酶联免疫吸附测定系统中,A2LA-1,A2LA-2和A2LA-3能够抑制ALA-1对大肠杆菌J5脂质A的反应性超过61%。用抗独特型抗体免疫的小鼠和兔子的血清显示,内部图像抗独特型抗体诱导了与脂质A交叉反应或结合的IgG抗体的产生。这些研究表明A2LA-1和A2LA-2含有模拟脂质A的抗原表位。用A2LA-1免疫小鼠可预防大肠杆菌J5脂多糖的致死毒性。

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