Epstein-Barr virus (EBV) replicative gene expression in tumour cells of AIDS-related non-Hodgkin's lymphoma in relation to CD4 cell number and antibody titres to EBV

AIDS. 1994 May;8(5):583-90. doi: 10.1097/00002030-199405000-00003.

Abstract

Objective: To determine whether activation of Epstein-Barr virus (EBV) replication in tumour cells of AIDS-related non-Hodgkin's lymphoma (ARNHL) is correlated with CD4+ cell counts and influences antibody response to EBV [anti-Z Epstein-Barr replicative activator (ZEBRA), anti-early antigen (EA), anti-viral capsid antigen (VCA)].

Design: Retrospective study based on immunohistochemistry and in situ hybridization to detect EBV replicative gene products in tissue samples from patients affected by ARNHL and correlation with CD4+ cell counts and results of EBV serology (including anti-ZEBRA activity) in sera from the same patients.

Methods: Seventeen out of 22 cases of ARNHL were selected for the presence of EBV [Epstein-Barr early region (EBER) RNA-positive]. Immunohistochemistry was performed with anti-ZEBRA, anti-EA-restricted, anti-VCA antibodies and in situ hybridization with BHLF1/NotI oligoprobes on tumour samples. Results were statistically correlated with those of CD4+ cell counts (17 out of 17) and with anti-EBV antibody titres (13 out of 17) assessed using standard immunofluorescence method and enzyme-linked immunosorbent assay procedure using recombinant ZEBRA protein and synthetic peptides as antigens.

Results: BZLF1 (ZEBRA) or early gene products (EA-R and EA-D/BHLF1/NotI) were detected in a small proportion (< 0.01-5%) of tumour cells in eight of these 17 cases by immunohistochemistry and in situ hybridization. Demonstration of replicative gene expression did not correlate with either low CD4+ cell counts (P > 0.05) or anti-EBV antibody titres (P > 0.05). Anti-ZEBRA activity was not significantly increased in patients affected with ARNHL, the cells of which expressed replicative gene products (P > 0.05).

Conclusion: The degree of immunodeficiency does not clearly enhance replicative gene expression in tumour cells of ARNHL. EBV serology, including anti-ZEBRA activity, is not a reliable tool for predicting the occurrence of such proliferations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acquired Immunodeficiency Syndrome / complications
  • Adult
  • Antibodies, Viral / biosynthesis
  • Antibodies, Viral / blood*
  • Antibody Specificity
  • Antigens, Viral / biosynthesis
  • Antigens, Viral / genetics
  • Antigens, Viral / immunology
  • CD4-Positive T-Lymphocytes*
  • Capsid Proteins*
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / immunology
  • Enzyme-Linked Immunosorbent Assay
  • Epstein-Barr Virus Nuclear Antigens
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Gene Expression Regulation, Viral*
  • Herpesviridae Infections / complications
  • Herpesvirus 4, Human / genetics*
  • Herpesvirus 4, Human / immunology
  • Herpesvirus 4, Human / physiology
  • Humans
  • Leukocyte Count
  • Lymphoma, AIDS-Related / microbiology*
  • Male
  • Middle Aged
  • Retrospective Studies
  • Trans-Activators / biosynthesis
  • Trans-Activators / genetics
  • Trans-Activators / immunology
  • Tumor Virus Infections / complications
  • Viral Proteins*
  • Virus Activation*
  • Virus Replication

Substances

  • Antibodies, Viral
  • Antigens, Viral
  • BZLF1 protein, Herpesvirus 4, Human
  • Capsid Proteins
  • DNA-Binding Proteins
  • Epstein-Barr Virus Nuclear Antigens
  • Epstein-Barr viral capsid antigen
  • Epstein-Barr virus early antigen
  • Trans-Activators
  • Viral Proteins