Kp. Flaming et al., PIGS ARE RELATIVELY RESISTANT TO DEXAMETHASONE-INDUCED IMMUNOSUPPRESSION, Comparative haematology international, 4(4), 1994, pp. 218-225
Dexamethasone administration has been widely used as a model of immuno
suppression in various species. The objective of the work reported her
e was to evaluate immune function in pigs treated with dexamethasone.
Experiment 1 pigs were assigned to either control (n = 10) or 2 mg/kg
dexamethasone (n = 10) treated groups. Treatments were administered 48
and 24 h before immune function testing. The dexamethasone-treated pi
gs received the drug on 22 of 72 experimental days. Pigs in experiment
2 were assigned to one of three groups: control (n = 10), 2 mg/kg dex
amethasone (n = 10), or 6 mg/kg dexamethasone (n = 10). Treatments wer
e given once and immune functions were evaluated 3 and 27 h after trea
tment. Lymphocyte blastogenesis, total and differential white blood ce
ll count, and several measures of in vitro neutrophil function were me
asured in both experiments. Antigen specific antibody production, grow
th rate, and organ weights at necropsy were also measured in experimen
t 1. There were no consistent changes in neutrophil functions in these
experiments. Lymphocyte blastogenesis to concanavalin A and pokeweed
mitogen was significantly (p <0.05) enhanced during experiment 1 in de
xamethasone-treated pigs; antigen specific antibody production was not
altered by treatment. Dexamethasone treatment (both 2 and 6 mg/kg) in
experiment 2 caused a profound (p <0.02-0.01) decrease in lymphocyte
blastogenesis to all three mitogens tested at 3 h after treatment. Lym
phocyte proliferation returned to control levels by 27 h after treatme
nt in experiment 2. Dexamethasone treatment was also associated with a
relative neutrophilia and lymphopenia in both experiments. Dexamethas
one-treated pigs in experiment 1 grew slower, had larger livers and ki
dneys, but smaller spleens than control animals. The transient decreas
e in lymphocyte blastogenesis, lack of consistent changes in neutrophi
l function, and unaltered antibody production despite treatment with l
arge doses of dexamethasone indicate that pigs are remarkably resistan
t to immunosuppression by this drug.