NIRF-Molecular Imaging with Synovial Macrophages-Targeting Vsig4 Nanobody for Disease Monitoring in a Mouse Model of Arthritis

Int J Mol Sci. 2019 Jul 8;20(13):3347. doi: 10.3390/ijms20133347.

Abstract

Nanobody against V-set and Ig domain-containing 4 (Vsig4) on tissue macrophages, such as synovial macrophages, could visualize joint inflammation in multiple experimental arthritis models via single-photon emission computed tomography imaging. Here, we further addressed the specificity and assessed the potential for arthritis monitoring using near-infrared fluorescence (NIRF) Cy7-labeled Vsig4 nanobody (Cy7-Nb119). In vivo NIRF-imaging of collagen-induced arthritis (CIA) was performed using Cy7-Nb119. Signals obtained with Cy7-Nb119 or isotope control Cy7-NbBCII10 were compared in joints of naive mice versus CIA mice. In addition, pathological microscopy and fluorescence microscopy were used to validate the arthritis development in CIA. Cy7-Nb119 accumulated in inflamed joints of CIA mice, but not the naive mice. Development of symptoms in CIA was reflected in increased joint accumulation of Cy7-Nb119, which correlated with the conventional measurements of disease. Vsig4 is co-expressed with F4/80, indicating targeting of the increasing number of synovial macrophages associated with the severity of inflammation by the Vsig4 nanobody. NIRF imaging with Cy7-Nb119 allows specific assessment of inflammation in experimental arthritis and provides complementary information to clinical scoring for quantitative, non-invasive and economical monitoring of the pathological process. Nanobody labelled with fluorescence can also be used for ex vivo validation experiments using flow cytometry and fluorescence microscopy.

Keywords: Nanobody; V-set and Ig domain-containing 4 (Vsig4); in vivo imaging; near- infrared fluorescence; synovial macrophage.

MeSH terms

  • Animals
  • Arthritis, Experimental / diagnosis*
  • Arthritis, Experimental / metabolism*
  • Fluorescent Antibody Technique
  • Fluorescent Dyes / chemistry
  • Immunohistochemistry
  • Macrophages / immunology
  • Macrophages / metabolism*
  • Male
  • Mice
  • Microscopy, Fluorescence
  • Models, Molecular
  • Molecular Imaging / methods*
  • Molecular Structure
  • Receptors, Complement* / immunology
  • Single-Domain Antibodies* / chemistry
  • Single-Domain Antibodies* / immunology
  • Spectroscopy, Near-Infrared
  • Staining and Labeling
  • Synovial Membrane / immunology
  • Synovial Membrane / metabolism*
  • Synovial Membrane / pathology*

Substances

  • Fluorescent Dyes
  • Receptors, Complement
  • Single-Domain Antibodies
  • VSIG4 protein, mouse