Gh. Reubel et al., EFFECTS OF INCIDENTAL INFECTIONS AND IMMUNE ACTIVATION ON DISEASE PROGRESSION IN EXPERIMENTALLY FELINE IMMUNODEFICIENCY VIRUS-INFECTED CATS, Journal of acquired immune deficiency syndromes, 7(10), 1994, pp. 1003-1015
Specific pathogen-free cats were experimentally infected with feline i
mmunodeficiency virus (FIV) and subsequently exposed to common infecti
ous pathogens and immune stimuli over a 3-year period. Cats with preex
isting FIV infection showed signs of disease after exposure to Haemoba
rtonella felis, Toxoplasma gondii, feline herpesvirus-1, and feline ca
licivirus similar to signs in non-FIV-infected cats, although they wer
e more severe. No adverse effects of immunization with inactivated rab
ies virus vaccine and a synthetic polyproline immunogen were observed
in either FIV-infected or non-FIV-infected cats, whereas the applicati
on of a diphtheria-tetanus-pertussis vaccine caused transient fever an
d lymphadenopathy in both groups of animals. Primary immune responses
to pathogens or immunogens were usually delayed or diminished in FIV-i
nfected compared with non-FIV-infected cats. Repeated infections and i
mmune activation had no significant effects on the levels of FIV-speci
fic antibodies or on the proportion of peripheral blood mononuclear ce
lls (PBMCs) containing FIV proviral DNA. However, FIV-infected cats th
at were not exposed to immune stimuli had lower CD4(+) T-lymphocyte nu
mbers and lower CD4(+)/CD8(+) T-lymphocyte ratios at the end of the 3-
year study than FIV-infected cats exposed to cofactors. The latter als
o had normal levels of interleukin-2 receptor (IL-2R) and major histoc
ompatibility class II (MHC-II) antigen expression on PBMCs, while FIV-
infected cats not exposed to cofactors had up-regulated IL-2R and down
-regulated MHC-II antigen expression. It was concluded that repeated i
mmune stimulation did not have a deleterious effect on the course of F
IV-induced immunodeficiency.