Department of Immunology, Graduate school of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8544, Japan.
Arthritis Res Ther. 2012 May 2;14(3):R106. doi: 10.1186/ar3831.
We previously demonstrated that synovial sublining macrophages express folate receptor beta (FRβ). The aim of this study was to evaluate the efficacy of intra-articular administration of a recombinant immunotoxin to FRβ for treating rat antigen-induced arthritis.
A monoclonal antibody (mAb) to rat FRβ was produced by immunizing mice with B300-19 cells (murine pre-B cells) transfected with the rat FRβ gene. Recombinant immunotoxin was prepared by conjugating the Fv portion of the anti-rat FRβ mAb heavy chain with a truncated Pseudomonas exotoxin A and the Fv portion of the anti-rat FRβ mAb light chain. Antigen-induced arthritis was induced through intra-articular injection of methylated bovine serum albumin (mBSA) after two subcutaneous injections of mBSA and complete Freund's adjuvant. Immunotoxin was intra-articularly injected into the arthritis joint every other day for seven days after arthritis onset. Joint swelling was measured and histological scores of inflammation, synovial thickness, cartilage, and bone destruction were determined. Immunohistochemistry was performed to detect osteoclast and osteoclast precursor FRβ-expressing macrophages and cathepsin K-positive cells on day 21.
Intra-articular administration of the immunotoxin attenuated joint swelling (61% suppression; P < 0.01 compared to the control on day 21) and improved histological findings, particularly cartilage and bone destruction (scores of rats treated with control versus the immunotoxin: 2.2 versus 0.5; P < 0.01), by reducing the number of FRβ-expressing macrophages and cathepsin K-positive cells.
Intra-articular administration of an immunotoxin to FRβ is effective for improving rat antigen-induced arthritis.
我们之前证明滑膜下衬里巨噬细胞表达叶酸受体β(FRβ)。本研究旨在评估关节内注射 FRβ 重组免疫毒素治疗大鼠抗原诱导关节炎的疗效。
通过用转染了大鼠 FRβ 基因的 B300-19 细胞(鼠前 B 细胞)免疫小鼠产生抗大鼠 FRβ 单克隆抗体(mAb)。通过将抗大鼠 FRβ mAb 重链的 Fv 部分与截短的铜绿假单胞菌外毒素 A 和抗大鼠 FRβ mAb 轻链的 Fv 部分缀合来制备重组免疫毒素。在两次皮下注射 mBSA 和完全弗氏佐剂后,通过关节内注射甲基化牛血清白蛋白(mBSA)诱导关节炎。关节炎发病后,每隔一天将免疫毒素关节内注射到关节炎关节中,共 7 天。测量关节肿胀,并确定炎症、滑膜厚度、软骨和骨破坏的组织学评分。在第 21 天,通过免疫组织化学检测破骨细胞和破骨细胞前体 FRβ 表达的巨噬细胞和组织蛋白酶 K 阳性细胞。
关节内注射免疫毒素减轻了关节肿胀(21 天时抑制率为 61%;与对照组相比,P < 0.01),改善了组织学发现,特别是软骨和骨破坏(对照组与免疫毒素治疗的大鼠评分:2.2 与 0.5;P < 0.01),减少了 FRβ 表达的巨噬细胞和组织蛋白酶 K 阳性细胞的数量。
关节内注射 FRβ 免疫毒素可有效改善大鼠抗原诱导的关节炎。