Bach M A, Beckmann E, Levitt D
Eur J Immunol. 1984 Jul;14(7):589-94. doi: 10.1002/eji.1830140702.
Immunization of mice with phosphorylcholine (PC)-bearing Staphylococcus pneumoniae Type 2, strain 36a (R36a) results in both a PC-specific and a polyclonal increase in splenic plaque-forming cells. The polyclonal increase was observed in all strains tested, including those bearing an X-linked immune defect resulting in an undetectable anti-PC immune response. The magnitude of the polyclonal response is directly related to the amount of bacterial surface PC as detected by enzyme-linked immunosorbent assay. Congenitally athymic (nude) mice mount an anti-PC plaque-forming cell response after R36a immunization but fail to produce a significant polyclonal response. From our results it appears that PC on the cell wall of a bacterium acts both as a polyclonal activator and a specific antigen, stimulating each by different mechanisms.
用含磷酰胆碱(PC)的2型肺炎链球菌36a菌株(R36a)免疫小鼠,会导致脾脏中形成斑块细胞的PC特异性增加以及多克隆增加。在所有测试菌株中均观察到多克隆增加,包括那些具有X连锁免疫缺陷导致无法检测到抗PC免疫反应的菌株。通过酶联免疫吸附测定法检测,多克隆反应的强度与细菌表面PC的量直接相关。先天性无胸腺(裸)小鼠在R36a免疫后会产生抗PC斑块形成细胞反应,但未能产生显著的多克隆反应。从我们的结果来看,细菌细胞壁上的PC既作为多克隆激活剂又作为特异性抗原,通过不同机制刺激两者。