Abstract

IntroductionWe 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.MethodsA 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.ResultsIntra-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.ConclusionsIntra-articular administration of an immunotoxin to FRβ is effective for improving rat antigen-induced arthritis.

Highlights

  • We previously demonstrated that synovial sublining macrophages express folate receptor beta (FRb)

  • We evaluated the efficacy of intra-articular administration of a recombinant immunotoxin to FRb for treating rat antigen-induced arthritis (AIA)

  • Specificity and reactivity of anti-rat FRb monoclonal antibody (mAb) Antibody clone 4A67 reacted with rat FRb gene-transfected cell lines (97.3 ± 0.3%) but did not react with the original cell lines (1.5 ± 0.2%) (Figure 1A)

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Summary

Introduction

We previously demonstrated that synovial sublining macrophages express folate receptor beta (FRb). Clinical disease activity in RA is strongly correlated with the number of macrophages in synovial tissues [3,4], and anti-TNF biological agents are thought to target synovial sublining. We previously reported that synovial sublining macrophages express folate receptor beta (FRb) as a receptor for oxidized folate [6,7]. These FRb-expressing macrophages predominantly expressed M1 macrophage markers [8]. In agreement with our previous study, several studies showed that RA synovial FRb-expressing macrophages may be potential targets for treating RA, utilizing the folate receptor (FR) as the drug delivery system [10,11]

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