Vingsbo-Lundberg C, Saxne T, Olsson H, Holmdahl R
Lund University, Sweden.
Arthritis Rheum. 1998 Mar;41(3):544-50. doi: 10.1002/1529-0131(199803)41:3<544::AID-ART21>3.0.CO;2-#.
To investigate the utility of serum cartilage oligomeric matrix protein (COMP) for disease monitoring in rats with chronic pristane-induced arthritis, and to examine the influence of age, sex, and genes on COMP concentrations in rat serum.
Serum COMP levels were quantified by immunoassay. Sera were obtained from DA, E3, and (E3 x DA)F1 rats each week between the ages of 4 and 30 weeks. The (E3 x DA)F2 (second generation after intercrossing) rats were injected intradermally with the synthetic oil pristane. Arthritis was monitored by a macroscopic scoring system, and serum levels of COMP were measured on days 6, 35, and 49 after immunization.
Serum levels of COMP decreased during growth, and reached a plateau after the age of 12 weeks. The DA rats had higher COMP levels than the E3 rats, and the (E3 x DA)F1 rats had intermediate levels. No differences were observed in these levels when the rats were grouped by sex. Arthritic (E3 x DA)F2 rats had increased serum concentrations of COMP on days 35 and 49 after pristane injection (P < 0.0001 versus the nonarthritic animals). COMP levels correlated with the severity of macroscopically detectable arthritis at both time points (r > 0.9). Rats with a chronic disease course were distinguished by higher serum concentrations of COMP during the acute stage than animals with similar clinical scores but with resolving arthritis (P < 0.01).
Serum analyses of COMP offer promise for monitoring tissue involvement in experimental arthritis. Such analyses should be useful for monitoring therapeutic interventions aimed at retarding tissue destruction as well as for studies of the genetically determined regulation of COMP turnover and susceptibility to arthritis. The application of molecular marker measurements to experimental arthritis offers a new possibility for verifying the utility of such measurements in human arthritis.
研究血清软骨寡聚基质蛋白(COMP)在慢性 pristane 诱导性关节炎大鼠疾病监测中的作用,并探讨年龄、性别和基因对大鼠血清 COMP 浓度的影响。
采用免疫分析法对血清 COMP 水平进行定量。在 4 至 30 周龄期间,每周从 DA、E3 及(E3×DA)F1 大鼠获取血清。对(E3×DA)F2(杂交后第二代)大鼠皮内注射合成油 pristane。通过宏观评分系统监测关节炎情况,并在免疫后第 6、35 和 49 天测量血清 COMP 水平。
血清 COMP 水平在生长过程中下降,12 周龄后达到平台期。DA 大鼠的 COMP 水平高于 E3 大鼠,(E3×DA)F1 大鼠的水平介于两者之间。按性别分组时,这些水平未观察到差异。关节炎(E3×DA)F2 大鼠在 pristane 注射后第 35 和 49 天血清 COMP 浓度升高(与非关节炎动物相比,P < 0.0001)。在两个时间点,COMP 水平均与宏观可检测到的关节炎严重程度相关(r > 0.9)。病程慢性的大鼠在急性期血清 COMP 浓度高于临床评分相似但关节炎正在缓解的动物(P < 0.01)。
血清 COMP 分析有望用于监测实验性关节炎中的组织受累情况。此类分析对于监测旨在延缓组织破坏的治疗干预以及研究 COMP 周转的基因决定调节和关节炎易感性的研究应是有用的。将分子标志物测量应用于实验性关节炎为验证此类测量在人类关节炎中的效用提供了新的可能性。