Transcription profile of chemokine receptors, cytokines and cytotoxic markers in peripheral blood of dogs with epitheliotropic cutaneous lymphoma

Vet Dermatol. 2013 Dec;24(6):628-31, e155. doi: 10.1111/vde.12076. Epub 2013 Oct 9.

Abstract

Background: Mycosis fungoides (MF) is the most common form of canine epitheliotropic cutaneous lymphoma, which is characterized by the accumulation of neoplastic CD8(+) T cells. Given that multifocal skin lesions are commonly seen in MF, neoplastic lymphocytes may actively migrate into the blood circulation.

Hypothesis/objectives: Cytotoxic T cells with a skin-homing phenotype could be increased in the blood circulation of dogs with MF.

Animals: Ten dogs with MF and 10 age-matched healthy dogs were included.

Methods: The transcription levels of chemokine receptors, cytokines and cytotoxic markers in peripheral blood of dogs with MF were quantified by real-time RT-PCR.

Results: The dogs with MF had lower transcription levels of chemokine receptors associated with skin homing (CCR4), epitheliotropism (CXCR3), lymph node homing (CCR7), a type-1 cytokine (LT-α) and cytotoxic markers (perforin and granzyme B) in the circulation than healthy control dogs (P < 0.05).

Conclusions and clinical importance: The present results suggest that the number of peripheral cytotoxic T cells with a skin-homing phenotype could be decreased in the peripheral blood of dogs with MF, which might be due to the sequestration of cytotoxic T cells in the lesional skin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers, Tumor / blood*
  • Case-Control Studies
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Dog Diseases / blood
  • Dog Diseases / metabolism*
  • Dogs
  • Gene Expression Regulation, Neoplastic
  • Mycosis Fungoides / genetics
  • Mycosis Fungoides / metabolism
  • Mycosis Fungoides / veterinary*
  • Receptors, Chemokine / genetics
  • Receptors, Chemokine / metabolism*
  • Transcriptome*

Substances

  • Biomarkers, Tumor
  • Cytokines
  • Receptors, Chemokine