Rimmelzwaan G F, Siebelink K H, Broos H, Drost G A, Weijer K, van Herwijnen R, Osterhaus A D
Laboratory of Immunobiology, National Institute of Public Health and Environmental Protection, Bilthoven, Netherlands.
Vet Microbiol. 1994 Mar;39(1-2):153-65. doi: 10.1016/0378-1135(94)90096-5.
In order to monitor the antibody response to feline immunodeficiency virus (FIV) in cats, following experimental and natural infection, enzyme-linked immunosorbent assays (ELISAs) were developed using recombinant env and gag proteins and p24-specific monoclonal antibodies. It was shown that in experimentally infected cats an env protein-specific antibody response was directly followed by a gag protein-specific response. Furthermore, an ELISA for the detection of env protein-specific serum antibodies proved more sensitive in identifying experimentally and naturally infected cats than ELISAs demonstrating gag protein-specific antibodies. It was concluded that, like in HIV infection of humans, the detection of env protein-specific serum antibodies in addition to gag protein-specific antibodies is not only an important tool in the diagnosis of the infection but also in studies concerning the pathogenesis of the disease.
为监测猫在实验性感染和自然感染后对猫免疫缺陷病毒(FIV)的抗体反应,利用重组env和gag蛋白以及p24特异性单克隆抗体开发了酶联免疫吸附测定(ELISA)。结果表明,在实验感染的猫中,env蛋白特异性抗体反应之后直接出现gag蛋白特异性反应。此外,用于检测env蛋白特异性血清抗体的ELISA在鉴定实验感染和自然感染的猫方面比检测gag蛋白特异性抗体的ELISA更敏感。得出的结论是,与人类HIV感染一样,除检测gag蛋白特异性抗体外,检测env蛋白特异性血清抗体不仅是感染诊断的重要工具,也是疾病发病机制研究的重要工具。