Immunohistochemical characterization of inflammatory cells and immunologic activation markers in muscle and nerve biopsy specimens from patients with systemic polyarteritis nodosa

Arthritis Rheum. 1994 Jul;37(7):1055-61. doi: 10.1002/art.1780370711.

Abstract

Objective: To investigate the phenotype of infiltrating cells in classic lesions of polyarteritis nodosa (PAN).

Methods: Twenty-one muscle and 10 sural nerve biopsy samples from 24 patients with systemic PAN were studied using avidin-biotin-peroxidase and alkaline phosphatase-anti-alkaline phosphatase immunohistochemical techniques.

Results: The inflammatory infiltrates consisted mainly of macrophages (41%) and T lymphocytes (41%), particularly of the CD4+ subset. Granulocytes were present in varying quantities (0-45%) and were more abundant in heavily infiltrated vessels and in those with fibrinoid necrosis. Dendritic cells could be identified in 4 samples. Proliferating and interleukin-2 receptor-expressing cells, present in 71% and 79% of the patients, respectively, were more frequent in untreated patients.

Conclusion: T cell-mediated immune mechanisms may play a role in the development and perpetuation of PAN lesions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Biopsy
  • CD4-CD8 Ratio
  • CD4-Positive T-Lymphocytes / chemistry
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / pathology
  • Female
  • Granulocytes / chemistry
  • Granulocytes / immunology
  • Granulocytes / pathology
  • Histocompatibility Antigens Class II / analysis
  • Humans
  • Immunohistochemistry
  • Macrophages / chemistry
  • Macrophages / immunology
  • Macrophages / pathology
  • Male
  • Middle Aged
  • Muscles / pathology*
  • Nerve Tissue / pathology*
  • Phenotype
  • Polyarteritis Nodosa / etiology*
  • Polyarteritis Nodosa / immunology
  • Polyarteritis Nodosa / pathology*
  • Receptors, Interleukin-2 / analysis
  • T-Lymphocytes / chemistry
  • T-Lymphocytes / immunology
  • T-Lymphocytes / pathology

Substances

  • Histocompatibility Antigens Class II
  • Receptors, Interleukin-2