Monitoring Therapy Response of Experimental Arthritis with Radiolabeled Tracers Targeting Fibroblasts, Macrophages, or Integrin αvβ3

J Nucl Med. 2016 Mar;57(3):467-72. doi: 10.2967/jnumed.115.162628. Epub 2015 Dec 3.

Abstract

Rheumatoid arthritis is an autoimmune disease resulting in chronic synovial inflammation. Molecular imaging could be used to monitor therapy response, thus enabling tailored therapy regimens and enhancing therapeutic outcome. Here, we hypothesized that response to etanercept could be monitored by radionuclide imaging in arthritic mice. We tested 3 different targets, namely fibroblast activation protein (FAP), macrophages, and integrin αvβ3.

Methods: Male DBA/1J mice with collagen-induced arthritis were treated with etanercept. SPECT/CT scans were acquired at 1, 24, and 48 h after injection of (111)In-RGD2 (integrin αvβ3), (111)In-anti-F4/80-A3-1 (antimurine macrophage antibody), or (111)In-28H1 (anti-FAP antibody), respectively, with nonspecific controls included. Mice were dissected after the last scan, and scans were analyzed quantitatively and were correlated with macroscopic scoring.

Results: Experimental arthritis was imaged with (111)In-28H1 (anti-FAP), (111)In-anti-F4/80-A3-1, and (111)In-RGD2. Tracer uptake in joints correlated with arthritis score. Treatment decreased joint uptake of tracers from 23 ± 15, 8 ± 4, and 2 ± 1 percentage injected dose per gram (%ID/g) to 11 ± 11 (P < 0.001), 4 ± 4 (P < 0.001), and 1 ± 0.2 %ID/g (P < 0.01) for (111)In-28H1, (111)In-anti-F4/80-A3-1, and (111)In-RGD2, respectively. Arthritis-to-blood ratios (in mice with arthritis score 2 per joint) were higher for (111)In-28H1 (5.5 ± 1; excluding values > 25), (111)In-anti-F4/80-A3-1 (10.4 ± 4), and (111)In-RGD2 (7.2 ± 1) than for control (111)In-DP47GS (0.7 ± 0.5; P = 0.002), (111)In-rat IgG2b (0.5 ± 0.2; P = 0.002), or coinjection of excess RGD2 (3.5), indicating specific uptake of all tracers in arthritic joints.

Conclusion: (111)In-28H1, (111)In-anti-F4/80-A3-1, and (111)In-RGD2 can be used to specifically monitor the response to therapy in experimental arthritis at the molecular level. Further studies, however, still need to be performed.

Keywords: RGD peptide; experimental arthritis; fibroblast activation protein; macrophages; therapy response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthritis, Experimental / diagnostic imaging*
  • Arthritis, Experimental / drug therapy
  • Arthritis, Experimental / metabolism*
  • Etanercept / therapeutic use
  • Fibroblasts / diagnostic imaging*
  • Integrin alphaVbeta3 / metabolism*
  • Joints / diagnostic imaging
  • Macrophages / diagnostic imaging*
  • Male
  • Mice
  • Mice, Inbred DBA
  • Oligopeptides / metabolism
  • Positron-Emission Tomography
  • Radiopharmaceuticals* / pharmacokinetics
  • Rats
  • Synovial Fluid / cytology
  • Synovial Fluid / metabolism
  • Tissue Distribution
  • Tomography, Emission-Computed, Single-Photon

Substances

  • Integrin alphaVbeta3
  • Oligopeptides
  • Radiopharmaceuticals
  • arginyl-glycyl-aspartic acid
  • Etanercept