Petty R E, Hunt D W, Mathers D M, McCormick A Q, Barker H, Southwood T R, Corson L
Department of Pediatrics, University of British Columbia, Vancouver, Canada.
J Rheumatol. 1994 Aug;21(8):1491-6.
To determine if the anterior uveitis associated with adjuvant arthritis (AA) in the rat can be passively transferred with arthritis to syngeneic recipients using spleen cells or T cell lines prepared from animals given complete Freund's adjuvant (CFA) and Mycobacterium butyricum (M. butyricum) in incomplete Freund's adjuvant (IFA).
Spleen cells from Lewis or Lewis SsN rats given IFA, CFA, type I collagen in IFA (CI-IFA), or type II collagen in IFA (CII-IFA) were administered to naive rats or rats treated with pertussis toxin or bacterial endotoxin. Three CD4+ T cell lines, propagated from CFA injected rats and maintained in vitro with M. butyricum (M-1), bovine proteoglycan (PR-1) or an extract of M. butyricum (MBE-1) were administered to naive or immunosuppressed rats. The arthritogenic and uveitogenic properties of these cell preparations and intradermal MBE-IFA, CII-IFA and intraperitoneal (ip) M. butyricum without adjuvant were evaluated.
Uveitis was observed in 15/69 (22%) arthritic rats given CFA. Spleen cells prepared from CFA injected rats caused arthritis in 55 (82%) and uveitis in 2 (3%) of 67 cell recipients. Uveitis occurred in 2/6 cell recipients pretreated with bacterial endotoxin. Neither uveitis nor arthritis was observed in rats given IFA (0/6) or spleen cells prepared from rats given IFA (0/27), CI-IFA (0/6), or CII-IFA (0/28). CII-IFA produced polyarthritis in 5/6 rats, but no uveitis. CII-IFA induced arthritis associated uveitis in 1/15 animals receiving spleen cells from rats given CII-IFA, but not those given CI-IFA (0/3) or IFA (0/13). Uveitis was observed in one recipient of the M-1 T cell line and in 2 recipients of the PR-1 T cell line. Immunization with 400 micrograms of MBE-IFA induced uveitis but not arthritis in 3/11 animals. The MBE specific T cell line was neither arthritogenic nor uveitogenic. A high frequency (5/6) of uveitis accompanied arthritis in male Lewis rats given ip M. butyricum. Arthritis occurred in 4/10 female Lewis rats given ip M. butyricum and 2 arthritic animals also developed uveitis.
Uveitis occurs infrequently in arthritic rats given spleen cells from CFA injected animals. The ip administration of M. butyricum constitutes a novel disease model in which the immunopathological relationships between arthritis and uveitis may be more reliably studied.
确定大鼠佐剂性关节炎(AA)相关的前葡萄膜炎是否可通过将从给予完全弗氏佐剂(CFA)和丁酸分枝杆菌(M. butyricum)于不完全弗氏佐剂(IFA)中的动物制备的脾细胞或T细胞系,被动转移至同基因受体的关节炎中。
将给予IFA、CFA、IFA中的I型胶原(CI-IFA)或IFA中的II型胶原(CII-IFA)的Lewis或Lewis SsN大鼠的脾细胞,给予未致敏大鼠或用百日咳毒素或细菌内毒素处理的大鼠。从注射CFA的大鼠中扩增并在体外与丁酸分枝杆菌(M-1)、牛蛋白聚糖(PR-1)或丁酸分枝杆菌提取物(MBE-1)一起维持培养的三个CD4 + T细胞系,给予未致敏或免疫抑制的大鼠。评估这些细胞制剂以及皮内MBE-IFA、CII-IFA和无佐剂的腹腔内(ip)丁酸分枝杆菌的致关节炎和致葡萄膜炎特性。
在给予CFA的69只关节炎大鼠中有15只(22%)观察到葡萄膜炎。从注射CFA的大鼠制备的脾细胞在67只细胞受体中有55只(82%)引起关节炎,2只(3%)引起葡萄膜炎。在用细菌内毒素预处理的6只细胞受体中有2只发生葡萄膜炎。给予IFA(0/6)或从给予IFA(0/27)、CI-IFA(0/6)或CII-IFA(0/28)的大鼠制备的脾细胞的大鼠中,未观察到葡萄膜炎或关节炎。CII-IFA在5/6大鼠中产生多关节炎,但无葡萄膜炎。CII-IFA在1/15只接受来自给予CII-IFA大鼠的脾细胞的动物中诱导关节炎相关性葡萄膜炎,但给予CI-IFA(0/3)或IFA(0/13)的动物未出现。在M-1 T细胞系的1只受体和PR-1 T细胞系的2只受体中观察到葡萄膜炎。用400微克MBE-IFA免疫在11只动物中有3只诱导了葡萄膜炎但未诱导关节炎。MBE特异性T细胞系既无致关节炎性也无致葡萄膜炎性。给予腹腔内丁酸分枝杆菌的雄性Lewis大鼠中,葡萄膜炎伴随关节炎的发生率很高(5/6)。给予腹腔内丁酸分枝杆菌的10只雌性Lewis大鼠中有4只发生关节炎,2只关节炎动物也发生了葡萄膜炎。
给予来自注射CFA动物的脾细胞的关节炎大鼠中,葡萄膜炎很少发生。腹腔内给予丁酸分枝杆菌构成一种新的疾病模型,其中关节炎和葡萄膜炎之间的免疫病理关系可能得到更可靠的研究。