Loftager M K, Eriksen L, Nielsen R
Department of Clinical Studies, Royal Veterinary and Agricultural University, Copenhagen, Denmark.
Res Vet Sci. 1993 Jan;54(1):57-62. doi: 10.1016/0034-5288(93)90011-4.
Mucosal and serum antibodies against Actinobacillus pleuropneumoniae serotype 2 were demonstrable in an ELISA which used whole bacterial cells as antigen. Following experimental infection of pigs with A pleuropneumoniae serotype 2, specific antibodies against the bacteria were demonstrated in saliva and fluid obtained by bronchoalveolar lavage. There was a good correlation between the IgA antibody titre in this fluid and serum. As a result of natural infection, IgA antibodies were also demonstrable in the saliva at an early stage of infection when no serum antibodies were detectable. Later in the infection, when antibodies were present in the serum, salivary IgA antibodies were undetectable. The data suggest that the mucosal IgA antibody response arises before the systemic response. Measuring mucosal antibodies in saliva or nasal or bronchoalveolar fluid might therefore open the possibility of identifying pigs infected with A pleuropneumoniae at an early stage of infection.
在一种使用全菌细胞作为抗原的酶联免疫吸附测定(ELISA)中,可检测到针对胸膜肺炎放线杆菌2型的黏膜抗体和血清抗体。在用胸膜肺炎放线杆菌2型对猪进行实验性感染后,在唾液和通过支气管肺泡灌洗获得的液体中检测到了针对该细菌的特异性抗体。该液体中的IgA抗体滴度与血清中的IgA抗体滴度具有良好的相关性。由于自然感染,在感染早期血清抗体无法检测到时,唾液中也可检测到IgA抗体。在感染后期,血清中出现抗体时,唾液中的IgA抗体则无法检测到。这些数据表明,黏膜IgA抗体反应先于全身反应出现。因此,检测唾液、鼻腔或支气管肺泡液中的黏膜抗体可能为在感染早期识别感染胸膜肺炎放线杆菌的猪提供可能。