CCL5 expression in panniculitic T-cell dyscrasias and its potential role in adipocyte tropism Academic Article uri icon

Overview

MeSH Major

  • Adipocytes, White
  • Chemokine CCL5
  • Lymphoma, T-Cell
  • Panniculitis
  • Paraproteinemias
  • Subcutaneous Fat
  • T-Lymphocytes
  • Tropism

abstract

  • Subcutaneous panniculitis-like T-cell lymphoma and gamma/delta T-cell lymphoma involving fat are unique among the hematologic dyscrasias because of their almost exclusive involvement of the subcutaneous fat with little tendency toward extracutaneous dissemination. The systemic manifestations associated with this lymphoma are largely the sequelae of cytokine production by neoplastic T cells found within the subcutaneous fat. We hypothesized that the basis of this localization could be due to an interactive microenvironment between the neoplastic cells and the adipocytes. Given the expression of CCR5 in adipocytes, we explored the expression of its ligand CCL5 in the subcutaneous infiltrates in subcutaneous panniculitis-like T-cell lymphoma, gamma/delta T-cell lymphoma and compared it with those in lupus erythematosus profundus (LEP). We found that CCL5 was expressed in a significantly higher percentage of lymphocytes in lymphomas compared with those in LEP (P < 0.01). Additionally, the upregulation of CCL5 in areas of necrosis involved by lymphoma contrasted with the minimal staining in the zones of degeneration/necrosis in the setting of LEP. We observed direct internalization of CCL5-positive lymphocytes within adipocytes based on ultrastructural studies. This study shows that the basis of the adipocyte tropism may reflect a unique interaction between CCL5-positive lymphocytes and CCR5 positive adipocytes. Given the known pharmacologic inhibitors of CCR5-expression one might propose that using such inhibitors (ie, anti-CCR5) could be of therapeutic value in select cases.

publication date

  • May 2013

Research

keywords

  • Academic Article

Identity

Language

  • eng

Digital Object Identifier (DOI)

  • 10.1097/DAD.0b013e31826b4b1a

PubMed ID

  • 23190507

Additional Document Info

start page

  • 332

end page

  • 7

volume

  • 35

number

  • 3