J Korean Med Sci.  1991 Sep;6(3):279-283. 10.3346/jkms.1991.6.3.279.

Human fibroblasts in idiopathic retroperitoneal fibrosis express HLA-DR antigens

Affiliations
  • 1Department of Pathology Asan Medical Center College of Medicine, Ulsan University Seoul, Korea.

Abstract

Idiopathic retroperitoneal fibrosis (IRF) is a rare human disease characterized by non-neoplastic fibroblastic proliferation associated with chronic inflammatory cells; its pathogenesis is obscure. We undertook an immunohistochemical study for the expression of HLA-DR antigens and other immune-related markers by retroperitoneal proliferating fibroblasts and inflammatory cells from 2 IRF patients. Patterns of immunoreactivity were compared with those expressed by human nodular fasciitis (NF) and granulation tissue. In IRF, most fibroblasts immunostained strongly for HLA-DR antigens, whereas fibroblasts in NF and granulation tissue did, not immunostain at all. The fibroblasts did not immunostain for interleukin 2 receptor, C3b receptor, CD-4, CD-8, or Leu-M1 in any of the tissue studied. Most macrophages and lymphocytes in IRF and NF immunostained Strangly for HLA-DR antigens. In IRF, the CD-4 and CD-8 immunostained T-lymphocytes appeared equally distributed. The expression of HLA-DR antigens by fibroblasts in IRF indicates that this rare disease may indeed be an immune-associated hypersensitivity disorder.

Keyword

Idiopathic retroperitoneal fibrosis; HLA-DR antigens

MeSH Terms

Adult
Aged
Biological Markers
Fasciitis/pathology
Fibroblasts/*immunology/pathology
Granulation Tissue/pathology
HLA-DR Antigens/*analysis
Humans
Male
Middle Aged
Retroperitoneal Fibrosis/*immunology/pathology
Biological Markers
HLA-DR Antigens
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