Relationship between tumor necrosis factor alpha and feline immunodeficiency virus expressions

L A Kraus1, W G Bradley, R W Engelman

  • 1Department of Medical Microbiology and Immunology, University of South Florida, Tampa 33612, USA.

Journal of Virology
|January 1, 1996
PubMed

Insights

Tumor necrosis factor alpha (TNF-alpha) production is closely linked with feline immunodeficiency virus (FIV) p26 core protein expression during acute FIV infection. This relationship changes as the infection progresses and antibodies develop.

Area of Science:

  • Veterinary Virology
  • Immunology
  • Molecular Biology

Background:

  • Feline immunodeficiency virus (FIV) is an important pathogen in cats.
  • Understanding the dynamics of FIV infection is crucial for developing effective treatments.

Purpose of the Study:

  • To investigate the temporal relationship between FIV p26 core protein expression, tumor necrosis factor alpha (TNF-alpha) production, and proviral DNA burden during acute FIV infection in cats.

Main Methods:

  • Sequential biopsies of spleen and lymph nodes, peripheral blood mononuclear cells, and serum were analyzed.
  • FIV proviral DNA, FIV p26 core protein, and TNF-alpha were quantified.
  • Immunoprecipitation and in vitro induction assays were performed.

Main Results:

  • TNF-alpha levels increased significantly preceding FIV viremia and remained elevated during active infection.
  • TNF-alpha and FIV p26 expression were co-localized in lymph nodes during viremia.
  • Both TNF-alpha and p26 levels decreased with antibody development and viremia clearance.
  • Proviral DNA burden reduced in peripheral blood but remained in lymph nodes post-viremia.

Conclusions:

  • TNF-alpha production and FIV p26 expression are intimately linked during acute FIV infection.
  • The dynamics of FIV infection involve complex interactions between viral components and host immune responses.
  • FIV provirus persists primarily in lymph nodes even after viremia clearance.

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