Brahn E, Tang C, Banquerigo M L
Division of Rheumatology, UCLA School of Medicine 90024-1670.
Arthritis Rheum. 1994 Jun;37(6):839-45. doi: 10.1002/art.1780370611.
To investigate the capacity of taxol, a microtubule stabilizer, to inhibit collagen-induced arthritis (CIA), a model of rheumatoid arthritis.
Louvain rats were immunized with type II collagen (day 0) to induce arthritis. Taxol was administered beginning on day 2 (prevention protocol) or at arthritis onset on day 9 (in either a high-dose or low-dose suppression protocol). Rats were assessed clinically and radiographically for arthritis severity. Cellular and humoral immune responses to type II collagen were also evaluated.
Institution of taxol prior to arthritis onset completely precluded the development of CIA (P < 0.0001 versus controls). It also suppressed established clinical disease (high-dose protocol P < 0.0000001; low-dose protocol P < 0.0001) and radiographic erosions (high-dose protocol P < 0.00001; low-dose protocol P < 0.001) compared with controls. Levels of IgG antibodies, but not delayed-type hypersensitivity, to type II collagen were reduced after taxol administration.
Taxol completely prevented the induction of CIA and caused significant regression of existing arthritis.
研究微管稳定剂紫杉醇抑制类风湿关节炎模型——胶原诱导性关节炎(CIA)的能力。
用II型胶原免疫鲁汶大鼠(第0天)以诱导关节炎。从第2天开始给予紫杉醇(预防方案)或在第9天关节炎发作时给予(高剂量或低剂量抑制方案)。对大鼠的关节炎严重程度进行临床和影像学评估。还评估了对II型胶原的细胞和体液免疫反应。
在关节炎发作前给予紫杉醇完全阻止了CIA的发展(与对照组相比,P<0.0001)。与对照组相比,它还抑制了已确立的临床疾病(高剂量方案P<0.0000001;低剂量方案P<0.0001)和影像学侵蚀(高剂量方案P<0.00001;低剂量方案P<0.001)。给予紫杉醇后,对II型胶原的IgG抗体水平降低,但迟发型超敏反应未降低。
紫杉醇完全预防了CIA的诱导,并使现有关节炎显著消退。