Loftager M K, Eriksen L, Aasted B, Nielsen R
Department of Clinical Studies, Royal Veterinary and Agricultural University, Copenhagen, Denmark.
Res Vet Sci. 1993 Nov;55(3):281-6. doi: 10.1016/0034-5288(93)90095-w.
To introduce antigen to the respiratory mucosa, killed Actinobacillus pleuropneumoniae with quil A as adjuvant was administered to pigs as an aerosol. Immunisation by this aerosol induced a marked IgA response in the bronchoalveolar and nasal fluids, and in the serum. Following challenge with live bacteria two weeks after the last exposure to the aerosol, the immunised pigs were protected from the severe pleuropneumonia which developed in non-immunised pigs. The immunised pigs had lower antibody titres in the mucosal fluids and serum after exposure to the challenge. The immune response after experimental infection of non-immunised animals was a weak IgA antibody response in the bronchoalveolar and nasal fluids, whereas the systemic immune response after challenge included both IgA and IgG antibodies.
为将抗原引入呼吸道黏膜,以Quil A作为佐剂的灭活胸膜肺炎放线杆菌被制成气雾剂给予猪。通过这种气雾剂进行免疫在支气管肺泡液、鼻液和血清中诱导了显著的IgA反应。在最后一次接触气雾剂两周后用活细菌进行攻毒,免疫的猪受到保护,未出现非免疫猪所发生的严重胸膜肺炎。攻毒后,免疫猪的黏膜液和血清中的抗体滴度较低。未免疫动物经实验感染后的免疫反应是支气管肺泡液和鼻液中出现微弱的IgA抗体反应,而攻毒后的全身免疫反应包括IgA和IgG抗体。