Changes in duodenal CD163-positive cells in dogs with chronic enteropathy after successful treatment

Innate Immun. 2018 Oct;24(7):400-410. doi: 10.1177/1753425918799865. Epub 2018 Sep 17.

Abstract

Chronic enteropathy (CE) in dogs is characterized retrospectively per treatment response as food-responsive enteropathy (FRE), antibiotic-responsive enteropathy (ARE), and immunosuppressant-responsive enteropathy (IRE) - the latter most resembling inflammatory bowel disease in people. The aim of this study was to characterize duodenal macrophages (Mϕ) in CE using immunohistochemistry; with calprotectin (CAL) as a marker of early differentiated Mϕ and CD163 expression as a marker for resident Mϕ in the duodenum before and after treatment. Prior to treatment, dogs with FRE and IRE had a lower CD163+/CAL+ ratio than control dogs (CTRL) in crypts; this increased significantly and normalized compared with CTRL after treatment. Conversely, the CD163+/CAL+ ratio in dogs with ARE was comparable to that in healthy dogs before and after treatment. In summary, these results suggest that Mϕ play a role in the pathogenesis of CE in FRE and IRE, with a decrease in resident Mϕ and an increase in early differentiated Mϕ, but not in ARE dogs. Mϕ normalize after successful treatment.

Keywords: CD163; Canine; chronic enteropathy; inflammatory bowel disease; macrophage.

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Biomarkers / metabolism
  • Cell Differentiation
  • Disease Models, Animal
  • Dogs
  • Duodenum / immunology*
  • Female
  • Humans
  • Immunohistochemistry
  • Inflammatory Bowel Diseases / drug therapy
  • Inflammatory Bowel Diseases / immunology*
  • Leukocyte L1 Antigen Complex / metabolism
  • Macrophages / immunology*
  • Male
  • Receptors, Cell Surface / metabolism
  • Retrospective Studies

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Biomarkers
  • CD163 antigen
  • Leukocyte L1 Antigen Complex
  • Receptors, Cell Surface