Progressive immune dysfunction in cats experimentally infected with feline immunodeficiency virus

J Virol. 1991 May;65(5):2225-30. doi: 10.1128/JVI.65.5.2225-2230.1991.

Abstract

Within 6 months of infection with the Petaluma isolate of feline immunodeficiency virus, specific-pathogen-free domestic cats exhibited a decrease in the percentage and number of circulating CD4+ lymphocytes and in the CD4+/CD8+ T-cell ratio, along with a marginally significant depression of pokeweed mitogen-induced lymphocyte proliferation in vitro. There was no loss of responsiveness to concanavalin A during this stage, and the cats were capable of mounting a satisfactory antibody response to a T-dependent, synthetic polypeptide immunogen. The pokeweed mitogen response deficit became clearly demonstrable by 11 to 12 months postinfection. A decline in the lymphocyte proliferative response to concanavalin A and a diminished ability to mount an in vivo antibody response to the T-dependent immunogen evolved by 25 to 44 months postinfection. Virus infection did not affect the ability of cats to mount an antibody response to a T-independent synthetic polypeptide immunogen. These data indicate that feline immunodeficiency virus produces a slowly progressive deterioration of T-cell function but does not affect the ability of B cells to recognize and respond to a T-independent antigenic stimulus.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antibodies, Viral / biosynthesis
  • Antigens, Differentiation, T-Lymphocyte
  • CD4 Antigens
  • CD4-Positive T-Lymphocytes / immunology
  • CD8 Antigens
  • Cats
  • Concanavalin A / pharmacology
  • Enzyme-Linked Immunosorbent Assay
  • Feline Acquired Immunodeficiency Syndrome / immunology*
  • Feline Acquired Immunodeficiency Syndrome / physiopathology
  • Immunodeficiency Virus, Feline / immunology
  • Molecular Sequence Data
  • Peptides / chemical synthesis
  • Peptides / immunology
  • Pokeweed Mitogens / pharmacology
  • Specific Pathogen-Free Organisms
  • T-Lymphocytes, Regulatory / immunology

Substances

  • Antibodies, Viral
  • Antigens, Differentiation, T-Lymphocyte
  • CD4 Antigens
  • CD8 Antigens
  • Peptides
  • Pokeweed Mitogens
  • Concanavalin A