Modulation of immune cell populations and activation markers in the pathogenesis of African swine fever virus infection

Virus Res. 1997 Jan;47(1):31-40. doi: 10.1016/s0168-1702(96)01403-7.

Abstract

African swine fever (ASF) virus induces immune cell alterations that may be detected by changes in peripheral blood cells phenotypic antigens and activation markers which were examined by flow cytometry, analyzing both cell proportion and/or expression intensity of superficial antigens. These studies were conducted in pigs with experimental acute of chronic ASF infection to determine whether changes among important surface activation markers and phenotypic antigens, and their correlative lymph node status, reflected similar or disparate aspects of immune pathology. In acute infection produced by virulent viruses, macrophage and B lymphocyte populations decreased in peripheral blood after a short activation period at the beginning of the infection. A significative decrease of interleukin 2 receptor (IL 2R) expression was also observed in those pigs. These variations correlated with lymph node cell depletion due to an intense lymphoid cell death by apoptosis, affecting mainly the B lymphocyte subpopulation as determined by immunohistochemistry. Nevertheless, pigs infected with an attenuated isolate undergoing chronic persistent infection, presented a distinct pattern of modification, according with a different clinicopathological evolution. Changes consisted in systemic immune activation coincident with the highest viremia titer, with an augmentation in CD8+ T lymphocyte, macrophage, and B cell populations, and MHC (major histocompatibility complex) antigens. Percentage elevation of circulating immune subpopulations was accompanied by cell accumulation with lymphoid hyperplasia but a conserved distribution of B lymphocytes in lymphoid organs of chronically infected pigs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • African Swine Fever / immunology*
  • African Swine Fever Virus / immunology*
  • African Swine Fever Virus / pathogenicity
  • Animals
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology*
  • Biomarkers
  • Cell Count
  • Chronic Disease
  • Lymphocyte Activation*
  • Lymphoid Tissue / immunology
  • Lymphoid Tissue / pathology
  • Macrophage Activation
  • Macrophages / cytology
  • Macrophages / immunology*
  • Swine
  • Swine, Miniature
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology*

Substances

  • Biomarkers