Saze K, Kinoshita C, Shiba F, Haga Y, Sudo T, Hashimoto K
Central Research Laboratories, Nippon Zenyaku Kogyo Co., Ltd., Fukushima, Japan.
J Vet Med Sci. 1994 Feb;56(1):97-102. doi: 10.1292/jvms.56.97.
Specific monoclonal antibodies (MoAbs) to Actinobacillus pleuropneumoniae (APP) serotypes 1 and 2 which recognized serotype-specific antigens were produced. It was revealed that the two serotype-specific MoAbs H1-18 and H22-7 recognized O polysaccharides of the lipopolysaccharide (LPS) from APP serotypes 1 and 2, respectively, in the results of antigen analysis by means of SDS-PAGE and Western blotting. Furthermore, ddY mice immunized passively with the above type-specific MoAbs were protected against challenge infection by the homologous serotype of APP at 24 or 48 hr later. However, H1-9 and H3-2 MoAbs recognizing serotype-common protein antigens of APP did not show signs of any protective effect. These results showed that LPS from APP bacterial cells was one of the structural substances in the serotype-specific antigens, and an important component as one of the antigens protecting against the homologous serotype strain.
制备了针对胸膜肺炎放线杆菌(APP)血清型1和2的特异性单克隆抗体(MoAbs),这些抗体可识别血清型特异性抗原。通过SDS-PAGE和蛋白质免疫印迹法进行抗原分析的结果显示,两种血清型特异性单克隆抗体H1-18和H22-7分别识别APP血清型1和2脂多糖(LPS)的O多糖。此外,用上述型特异性单克隆抗体被动免疫的ddY小鼠在24或48小时后可免受同源血清型APP的攻击感染。然而,识别APP血清型共同蛋白抗原的H1-9和H3-2单克隆抗体未显示出任何保护作用的迹象。这些结果表明,APP细菌细胞的LPS是血清型特异性抗原中的结构物质之一,也是抵抗同源血清型菌株的抗原的重要组成部分。