Cannon G W, Harper D S, Clayton F, Griffiths M M
Salt Lake City Veterans Affairs Medical Center, Utah 84148.
Autoimmunity. 1993;15(4):267-74. doi: 10.3109/08916939309115748.
Adjuvant-induced arthritis (AIA) can be passively transferred in Dark Agouti (DA) rats by spleen and lymph node cells after culture with Concanavalin A (Con A). A model not requiring in vitro Con A expansion and activation would be important in investigations of anti-rheumatic drugs in AIA. A new model using irradiated recipients fills this need. Donor DA rats treated with 0.1 ml complete Freund's adjuvant (CFA) containing 7.5 mg M. butyricum/ml were sacrificed 11 days after CFA injection, donor spleen cells harvested, and donor spleen cells injected intravenously into recipient DA rats previously irradiated with 5 Gy. Recipient rats developed arthritis 4-14 days after spleen cell transfer. This model can now be used to further define the effects of anti-rheumatic drugs in the passive transfer of AIA by eliminating the need for the in vitro Con A-induced expansion and/or activation of donor cells.
佐剂性关节炎(AIA)可通过用伴刀豆球蛋白A(Con A)培养后的脾脏和淋巴结细胞在暗褐鼠(DA)中被动转移。在AIA抗风湿药物研究中,一种不需要体外Con A扩增和激活的模型将很重要。一种使用经辐照受体的新模型满足了这一需求。用含7.5mg丁酸分枝杆菌/毫升的0.1毫升完全弗氏佐剂(CFA)处理的供体DA大鼠在CFA注射后11天处死,收获供体脾细胞,并将供体脾细胞静脉注射到先前接受5 Gy照射的受体DA大鼠中。受体大鼠在脾细胞转移后4-14天出现关节炎。该模型现在可用于进一步确定抗风湿药物在AIA被动转移中的作用,因为它无需体外Con A诱导供体细胞的扩增和/或激活。