Sugawara T, Takada S, Furuhama K, Takayama S, Nomura M, Kato M
Drug Safety Research Center, Daiichi Pharmaceutical Co. Ltd, Tokyo, Japan.
Int J Exp Pathol. 1995 Jun;76(3):191-9.
Muramyl dipeptide-Lys(L18) given by daily subcutaneous injection for 14 days induced arthritis in male Lewis, Fischer and nude rats, to a lesser degree in the last two than in the first strain. On the other hand, a single intradermal administration of Freund's complete adjuvant induced arthritis in Lewis and Fischer but not nude rats. Cyclosporin A (CsA) co-administered for 14 days markedly exacerbated the muramyl dipeptide-Lys(L18) induced arthritis (MIA) in rats of all three strains, but completely blocked the development of the adjuvant induced arthritis (AIA) in Lewis rats. Furthermore, AIA was transferred to recipient Lewis rats through spleen cells obtained from the donors with AIA, whereas MIA was not. Antibodies against type II collagen and DNA were not detected in sera from MIA or AIA rats. These data show a clear difference between MIA and AIA in the pattern of development of arthritis and suggest that delayed hypersensitivity reactions may be involved in the pathogenetic mechanisms of AIA, but not in MIA.
每天皮下注射14天的胞壁酰二肽-赖氨酸(L18)可诱导雄性刘易斯大鼠、费希尔大鼠和裸鼠发生关节炎,后两种大鼠发生关节炎的程度比第一种大鼠轻。另一方面,单次皮内注射弗氏完全佐剂可诱导刘易斯大鼠和费希尔大鼠发生关节炎,但不能诱导裸鼠发生关节炎。连续14天联合使用环孢素A(CsA)可显著加重所有三种品系大鼠的胞壁酰二肽-赖氨酸(L18)诱导的关节炎(MIA),但完全阻断刘易斯大鼠佐剂诱导的关节炎(AIA)的发展。此外,AIA可通过从患有AIA的供体获得的脾细胞转移至受体刘易斯大鼠,而MIA则不能。在MIA或AIA大鼠的血清中未检测到抗II型胶原和DNA抗体。这些数据表明MIA和AIA在关节炎发展模式上存在明显差异,并提示迟发型超敏反应可能参与AIA的发病机制,但不参与MIA的发病机制。