TY - JOUR
T1 - Enhancement of porcine natural killer cell activity by recombinant human and murine IL-12
AU - Cho, Daeho
AU - Lee, Wang J.
AU - Halloran, Patrick J.
AU - Trinchieri, Giorgio
AU - Kim, Yoon B.
N1 - Funding Information:
1This work was supported in part by Public Health Service Grant RO1 CA52090 awarded by the National Cancer Institute, National Institutes of Health, United States Department of Health and Human Services.
PY - 1996/8/25
Y1 - 1996/8/25
N2 - These studies describe the effects of recombinant human (rHu) and recombinant murine (rMu) interleukin 12 (IL-12) in the porcine system. To examine the effects of rHu and rMu IL-12, porcine PBL were cultured with rHu and rMu IL-12, and then used for a NK assay. Significant enhancement of porcine NK cell cytotoxicity was observed, and maximal enhancement was reached after 26 hr culture in nanogram quantities (5 ng/ml = 10 units/ml) of rHu and rMu IL-12. MonoclonaI antibody (mAb) specific for human IL-12, C8.6, blocked rHu IL-12 enhanced porcine natural killer (NK) cytotoxicity. It was also shown that rHu IL-12 had additive effects on enhancement of NK cell cytotoxicity with PNK-E/G7 mAbs which react with cytolytic trigger molecules on porcine NK cells. By using purified NK cells, porcine tumor necrosis factor-α (TNF-α) secretion was measured on rHu IL-12 and PNK-E/G7 mAb-activated NK cells. rHu IL-12 and PNK-E/G7 mAbs synergize to induce TNF-α secretion. These data indicate that rHu and rMu IL-12 are cross-reactive in the porcine system and suggest the potential use of the porcine system as an important animal model for further study of rHu IL-12.
AB - These studies describe the effects of recombinant human (rHu) and recombinant murine (rMu) interleukin 12 (IL-12) in the porcine system. To examine the effects of rHu and rMu IL-12, porcine PBL were cultured with rHu and rMu IL-12, and then used for a NK assay. Significant enhancement of porcine NK cell cytotoxicity was observed, and maximal enhancement was reached after 26 hr culture in nanogram quantities (5 ng/ml = 10 units/ml) of rHu and rMu IL-12. MonoclonaI antibody (mAb) specific for human IL-12, C8.6, blocked rHu IL-12 enhanced porcine natural killer (NK) cytotoxicity. It was also shown that rHu IL-12 had additive effects on enhancement of NK cell cytotoxicity with PNK-E/G7 mAbs which react with cytolytic trigger molecules on porcine NK cells. By using purified NK cells, porcine tumor necrosis factor-α (TNF-α) secretion was measured on rHu IL-12 and PNK-E/G7 mAb-activated NK cells. rHu IL-12 and PNK-E/G7 mAbs synergize to induce TNF-α secretion. These data indicate that rHu and rMu IL-12 are cross-reactive in the porcine system and suggest the potential use of the porcine system as an important animal model for further study of rHu IL-12.
UR - http://www.scopus.com/inward/record.url?scp=0030601318&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0030601318&partnerID=8YFLogxK
U2 - 10.1006/cimm.1996.0211
DO - 10.1006/cimm.1996.0211
M3 - Article
C2 - 8806803
AN - SCOPUS:0030601318
SN - 0008-8749
VL - 172
SP - 29
EP - 34
JO - Cellular Immunology
JF - Cellular Immunology
IS - 1
ER -