Collen T, McCullough K C, Doel T R
J Virol. 1984 Nov;52(2):650-5. doi: 10.1128/JVI.52.2.650-655.1984.
Cultures of spleen cells from immunized mice were stimulated in vitro by soluble preparations of purified foot-and-mouth disease virus. Virus-specific antibody, as detected by an enzyme-linked immunosorbent assay, was produced by immune spleen cells but not by normal, nonimmune cells. The optimal specific response was obtained with 1 microgram of virus per ml of culture; as the virus concentration was increased, the production of specific antibody was reduced. For very low concentrations of virus (less than 0.01 microgram per culture), there was tentative evidence of suppression of the specific antibody response. The levels of specific antibody induced were dependent on the source and number of plastic-adherent cells present in the cultures. We intend to use this model system to study further the basis of immunity to foot-and-mouth disease virus.
用纯化的口蹄疫病毒可溶性制剂在体外刺激免疫小鼠的脾细胞培养物。通过酶联免疫吸附测定法检测到,病毒特异性抗体由免疫脾细胞产生,而非正常的非免疫细胞。每毫升培养物中加入1微克病毒可获得最佳特异性反应;随着病毒浓度增加,特异性抗体的产生减少。对于极低浓度的病毒(每培养物少于0.01微克),有初步证据表明特异性抗体反应受到抑制。诱导产生的特异性抗体水平取决于培养物中塑料贴壁细胞的来源和数量。我们打算利用这个模型系统进一步研究对口蹄疫病毒免疫的基础。