NEONATAL TREATMENT WITH LUTEINIZING-HORMONE-RELEASING HORMONE ANALOGSALTERS PERIPHERAL LYMPHOCYTE SUBSETS AND CELLULAR AND HUMORALLY MEDIATED IMMUNE-RESPONSES IN JUVENILE AND ADULT MALE MONKEYS
Dr. Mann et al., NEONATAL TREATMENT WITH LUTEINIZING-HORMONE-RELEASING HORMONE ANALOGSALTERS PERIPHERAL LYMPHOCYTE SUBSETS AND CELLULAR AND HUMORALLY MEDIATED IMMUNE-RESPONSES IN JUVENILE AND ADULT MALE MONKEYS, The Journal of clinical endocrinology and metabolism, 78(2), 1994, pp. 292-298
We examined the effect of treatment with a LH-releasing hormone (LHRH)
agonist (Ag), antagonist (Ant), or Ant and androgen (Ant/And) for the
first 4 months of postnatal life on lymphocyte subsets and cellular a
nd humorally mediated immune responses in juvenile and adult male monk
eys. We also determined the effect of 9 weeks of Ant treatment on lymp
hocyte subsets in adult male monkeys. Adult male monkeys that had been
treated neonatally with an Ag had increased levels of CD8-positive (C
D8(+)) T-cells and reduced levels of B-cells compared to vehicle-treat
ed controls. Lymphocytes from these animals also showed an elevated pr
oliferative response to a variety of mitogens compared to cells from c
ontrol animals. Antibody production in response to tetanus toroid was
normal in treated animals. Other neonates treated with Ant/And exhibit
ed subnormal levels of lymphocytes, CD8(+) T-cells, and B-cells at 4 m
onths of age. Similar changes, but of lesser magnitude, were observed
in animals treated with Ant alone. At 6 months of age, lymphocytes fro
m both groups of Ant-treated monkeys exhibited an above normal prolife
rative response to streptolysin-0, but not to other mitogens. At 18 mo
nths of age, animals treated with Ant alone produced more antitetanus
antibody in response to a tetanus toroid booster than the controls or
Ant/And-treated animals. Ant treatment was without major effect on lym
phocyte subsets in adult monkeys. Serum LH and testosterone levels dec
lined, and there was a small but significant increase in B-cells, lymp
hocytes expressing the interleukin-2 receptor, and the CD4(+)/CD8(+) T
-cell ratio during treatment, but these parameters normalized during t
he posttreatment period. The data suggest that chronic neonatal treatm
ent with an Ag or Ant alters the development of immune system response
s in male primates. The significance of these changes and their impact
on the ability of these animals to respond to pathogenic agents is un
der investigation.