The role of Mig, the monokine induced by interferon-gamma, and IP-10, the interferon-gamma-inducible protein-10, in tissue necrosis and vascular damage associated with Epstein-Barr virus-positive lymphoproliferative disease

Blood. 1997 Nov 15;90(10):4099-105.

Abstract

The mechanisms of tissue necrosis and vascular damage characteristics of certain Epstein-Barr virus (EBV)-associated lymphoproliferative disorders are unknown. The CXC chemokines interferon-gamma-inducible protein-10 (IP-10) and the monokine induced by interferon-gamma (Mig) caused tissue necrosis and vascular damage in Burkitt's lymphoma tumors established in nude mice. We report higher levels of IP-10 and Mig gene expression in tissues with necrosis and vascular damage from EBV-positive lymphomatoid granulomatosis and nasal or nasal-type T/natural killer (NK)-cell lymphomas compared with tissues with lymphoid hyperplasia, which lacked tissue necrosis and vascular damage. By immunohistochemistry, Mig and IP-10 proteins localized with similar patterns in viable tissue surrounding dead tissue, mostly within endothelial cells, monocyte/macrophages, and lymphocytes. Circulating levels of IP-10 were abnormally elevated in patients with EBV-positive lymphomatoid granulomatosis and nasal or nasal-type T/NK-cell lymphomas. These experiments provide the first description of the presence of Mig in any human normal or diseased tissue and the first description of IP-10 in certain lymphoproliferative lesions. These data suggest that Mig and IP-10 play an important role in the pathogenesis of tissue necrosis and vascular damage associated with certain EBV-positive lymphoproliferative processes.

MeSH terms

  • Adult
  • Animals
  • Blood Vessels / pathology*
  • Chemokine CXCL10
  • Chemokine CXCL9
  • Chemokines / biosynthesis*
  • Chemokines, CXC*
  • Female
  • Gene Expression Regulation, Neoplastic
  • Herpesviridae Infections / metabolism
  • Herpesviridae Infections / pathology*
  • Herpesviridae Infections / virology
  • Herpesvirus 4, Human / isolation & purification*
  • Humans
  • Intercellular Signaling Peptides and Proteins*
  • Interferon-gamma / metabolism
  • Lymphoproliferative Disorders / metabolism
  • Lymphoproliferative Disorders / pathology*
  • Lymphoproliferative Disorders / virology
  • Male
  • Mice
  • Middle Aged
  • Necrosis
  • Tumor Virus Infections / metabolism
  • Tumor Virus Infections / pathology*
  • Tumor Virus Infections / virology

Substances

  • CXCL9 protein, human
  • Chemokine CXCL10
  • Chemokine CXCL9
  • Chemokines
  • Chemokines, CXC
  • Intercellular Signaling Peptides and Proteins
  • Interferon-gamma