Gb. Schneider et M. Relfson, EFFECTS OF INTERLEUKIN-2 ON BONE-RESORPTION AND NATURAL IMMUNITY IN OSTEOPETROTIC (IA) RATS, Lymphokine and cytokine research, 13(6), 1994, pp. 335-341
Cells of the immune system and the cytokines they produce have been sh
own to function in the regulation of bone turnover. Incisors absent (i
a) osteopetrotic rats demonstrate defects in natural immunity and bone
resorption, even though they have excess numbers of both natural kill
er (NK) cells and osteoclasts. In an attempt to correct these defects,
mutant (ia) and normal rats were infused with 3 x 10(4) U recombinant
interleukin-2 (rIL-2)/day for 14 days using osmotic minipumps. The ef
fects of IL-2 on natural immune function and bone resorption were eval
uated after the infusion period. The percentage of NK cells in the spl
een after treatment was quantitated by phenotypic analysis using monoc
lonal antibodies and flow cytometry. The elevated levels of NK cells n
ormally seen in ia mutants were reduced to normal in the IL-2-infused
rats. NK cell activity was evaluated by the Cr-51 release assay and fo
und to be enhanced to normal killing levels in the IL-2-treated mutant
s. The defects in NK function are corrected by IL-2 therapy. Likewise,
the bone resorption defect appears to be corrected by the IL-2 infusi
ons. The bone marrow cavity size was significantly increased in the IL
-2-treated mutants compared with control mutants. Additionally, the pe
rcentage of osteoclasts exhibiting normal morphology was significantly
increased in the IL-2-treated mutants. The bone density of the caudal
vertebrae, evaluated by gray-scale analysis of x-rays, was found to b
e reduced in the IL-2-treated mutants. Interleukin-2 corrects both the
bone resorption and natural immune defects in the ia mutation.