Regression of collagen-induced arthritis with taxol, a microtubule stabilizer
β Scribed by Ernest Brahn; Chris Tang; Mona Lisa Banquerigo
- Book ID
- 102754373
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 622 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0004-3591
No coin nor oath required. For personal study only.
β¦ Synopsis
Objective. To investigate the capacity of taxol, a microtubule stabilizer, to inhibit collagen-induced arthritis (CIA), a model of rheumatoid arthritis.
Methods. Louvain rats were immunized with type I1 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 I1 collagen were also evaluated.
Results. 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; lowdose protocol P < 0.001) compared with controls. Levels of IgG antibodies, but not delayed-type hypersensitivity, to type I1 collagen were reduced after taxol administration.
Conclusion. Taxol completely prevented the induction of CIA and caused significant regression of existing arthritis.
Collagen-induced arthritis (CIA) is a T celldependent animal model of rheumatoid arthritis (RA) (1). Within 2 weeks after immunization with type I1 collagen (CII) in Freund's incomplete adjuvant (FIA), susceptible rats develop polyarthritis with histologic
π SIMILAR VOLUMES
## Objective. Early treatment based on an early diagnosis of rheumatoid arthritis (RA) could halt progression of the disease, but early diagnosis is often difficult. Matrix metalloproteinase 3 (MMP -3 ) is thought to be particularly important in the pathogenesis of RA. The aim of this study was