Kleinau S, Klareskog L
Department of Clinical Immunology, University Hospital, Uppsala, Sweden.
J Autoimmun. 1993 Aug;6(4):449-58. doi: 10.1006/jaut.1993.1037.
Passive transfer experiments were performed to investigate the role of immune cells and sera in the development of oil-induced arthritis (OIA) in DA rats. Con A-stimulated lymph node cells (LNC) obtained from animals previously injected with Freund's incomplete adjuvant (FIA) caused arthritis in irradiated recipients after intravenous administration. Also, enriched T-cell populations from these Con A-activated cells were able to transfer arthritis. Neither Con A-activated LNC from control rats (non-FIA-injected animals) nor sera from OIA animals were able to transfer arthritis. The passively transferred arthritis was evident clinically as well as histologically and the arthritic lesions were similar in many respects to those noted in the active OIA. The results thus provide strong evidence for an immunological etiology of oil-induced arthritis, and also suggest that autoreactive T cells are involved in the pathogenesis of the disease.
进行了被动转移实验,以研究免疫细胞和血清在DA大鼠油诱导性关节炎(OIA)发病过程中的作用。从先前注射弗氏不完全佐剂(FIA)的动物获得的刀豆蛋白A(Con A)刺激的淋巴结细胞(LNC),静脉注射后可使受辐照的受体发生关节炎。此外,来自这些Con A激活细胞的富集T细胞群体能够转移关节炎。来自对照大鼠(未注射FIA的动物)的Con A激活的LNC和OIA动物的血清均不能转移关节炎。被动转移的关节炎在临床和组织学上都很明显,并且关节炎病变在许多方面与活动性OIA中观察到的病变相似。因此,这些结果为油诱导性关节炎的免疫病因提供了有力证据,也表明自身反应性T细胞参与了该疾病的发病机制。