EFFECTS OF PCB (AROCLOR-1254) ON NONSPECIFIC IMMUNE PARAMETERS IN RHESUS (MACACA-MULATTA) MONKEYS

被引:43
作者
TRYPHONAS, H
LUSTER, MI
WHITE, KL
NAYLOR, PH
ERDOS, MR
BURLESON, GR
GERMOLEC, D
HODGEN, M
HAYWARD, S
ARNOLD, DL
机构
[1] GEORGE WASHINGTON UNIV, MED CTR, DEPT BIOCHEM & MOLEC BIOL, WASHINGTON, DC 20037 USA
[2] US EPA, HLTH EFFECTS RES LAB, RES TRIANGLE PK, NC 27711 USA
[3] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, DEPT PHARMACOL, RICHMOND, VA 23298 USA
[4] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, DEPT TOXICOL, RICHMOND, VA 23298 USA
[5] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, DEPT BIOSTAT, RICHMOND, VA 23298 USA
[6] NIEHS, IMMUNOTOXICOL GRP, RES TRIANGLE PK, NC 27709 USA
来源
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY | 1991年 / 13卷 / 06期
关键词
D O I
10.1016/0192-0561(91)90176-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The effects of low level, chronic polychlorinated biphenyl - Aroclor(R) 1254 - (PCB) exposure were investigated on non-specific immune parameters in female rhesus (Macaca mulatta) monkeys. Five groups of monkeys were orally administered with PCB at concentrations of 0, 5, 20, 40 or 80-mu-g/kg bw/day. Immunotoxicity testing was initiated after 55 months of exposure. The serum hemolytic complement activity in all PCB treated groups was significantly higher (P < 0.05) than that in the control group. A statistically significant dose-related increase in natural killer cell activity was evident at the 75 : 1 effector to target cell ratio. Similarly, a statistically significant dose-related increase was noted for thymosin alpha-1 levels but not for thymosin beta-4 levels. Statistically significant increased interferon levels were noted in the 20 and 80-mu-g/kg groups compared with the control group while the levels in the 40-mu-g/kg group were decreased significantly compared with the control group. The production of tumor necrosis factor by monocytes in the PCB treated groups was not different to that in the control group. The results indicated that long term exposure to PCB modulate several non-specific immune parameters.
引用
收藏
页码:639 / 648
页数:10
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