Thirkill C E, Muchmore H G, Hyde R M, Scott L V
In Vitro. 1981 May;17(5):405-11. doi: 10.1007/BF02626740.
The pathogenesis of the intra-articular, arthritic-inflammatory reaction caused by Mycoplasma arthritidis in susceptible rats and mice is poorly understood. To investigate this problem, synovial cells from normal Sprague-Dawley rats were cultured and studied in vitro. These cells continued to produce hyaluronic acid as measured by viscosity and chemical assays. Normal synovial cells were treated with rabbit serum specimens taken before and after immunization with M. arthritidis. Cytotoxicity assays indicated that the cells were killed in the presence of rabbit anti-M. arthritidis serum but not with preimmunization serum specimens. The anti-M. arthritidis serum was not cytotoxic to monolayer cultures of HEp-2, Vero, or L-cells. Antiserum produced in response to M. fermentans, M. hominis, and M. pulmonis did not produce a cytotoxic effect on the cultured synovial cells. From immunofluorescence studies it was demonstrated that the interactions occurred between the rabbit anti-M. arthritidis serum and synovial cell surface antigens. Extreme precautions were taken to prevent mycoplasmal contamination of rats and the synovial cells in culture. These observations would appear to support previous reports implicating mycoplasmas as biological triggering mechanisms of autoimmune reactions.
关节炎支原体在易感大鼠和小鼠中引发的关节内炎性反应的发病机制尚不清楚。为了研究这个问题,对正常斯普拉格-道利大鼠的滑膜细胞进行了体外培养和研究。通过粘度和化学分析测量,这些细胞持续产生透明质酸。用关节炎支原体免疫前后采集的兔血清标本处理正常滑膜细胞。细胞毒性试验表明,在兔抗关节炎支原体血清存在的情况下细胞被杀死,但在免疫前血清标本存在时细胞未被杀死。抗关节炎支原体血清对HEp-2、Vero或L细胞的单层培养物无细胞毒性。针对发酵支原体、人型支原体和肺支原体产生的抗血清对培养的滑膜细胞未产生细胞毒性作用。免疫荧光研究表明,兔抗关节炎支原体血清与滑膜细胞表面抗原之间发生了相互作用。采取了极端措施以防止大鼠和培养中的滑膜细胞受到支原体污染。这些观察结果似乎支持了先前将支原体作为自身免疫反应生物学触发机制的报道。