Levitt D, Corlett R
Guthrie Research Institute, Sayre, PA 18840.
J Immunol. 1988 Jan 1;140(1):273-6.
We investigated the cycle of immune enhancement and suppression seen in mice infected with Chlamydia trachomatis by using in vivo and in vitro model systems. BALB/c mice injected intravenously with chlamydia reveal a three- to seven-fold increase in numbers of plaque-forming cells producing antibodies against sheep red blood cells (SRBC), when immunized with SRBC 0 to 5 days after chlamydia infection. When mice are injected with SRBC 10 to 15 days after initial chlamydia infection, the specific anti-SRBC plaque-forming cell response is suppressed two- to three-fold. In vitro, low numbers (2 to 5 X 10(6) bacteria/ml) of chlamydia stimulate potent proliferative responses by B lymphocytes while high numbers (25 X 10(6) bacteria/ml) of bacteria generate strong, general T suppressor activity. This model has important implications for regulation of immune responses that arise at different times during chlamydial infections, as well as for the potential effectiveness of chlamydial vaccines.
我们通过体内和体外模型系统,研究了感染沙眼衣原体的小鼠体内出现的免疫增强和抑制循环。静脉注射衣原体的BALB/c小鼠,在衣原体感染后0至5天用绵羊红细胞(SRBC)免疫时,产生抗SRBC抗体的噬斑形成细胞数量增加了三到七倍。当小鼠在初次衣原体感染后10至15天注射SRBC时,特异性抗SRBC噬斑形成细胞反应被抑制了两到三倍。在体外,低数量(2至5×10⁶细菌/毫升)的衣原体刺激B淋巴细胞产生强烈的增殖反应,而高数量(25×10⁶细菌/毫升)的细菌则产生强大的、一般性的T抑制活性。该模型对于衣原体感染不同时期出现的免疫反应调节以及衣原体疫苗的潜在有效性具有重要意义。