Effects of toxaphene on the immune system of cynomolgus (Macaca fascicularis) monkeys. A pilot study.

Food Chem Toxicol

Toxicology Research Division, PL2202D1, Bureau of Chemical Safety, Canada.

Published: January 2000

AI Article Synopsis

  • Toxaphene was administered to cynomolgus monkeys at a daily dose of 1mg/kg for 52 weeks to study its effects on immune function.
  • Testing revealed potential immunosuppressive effects, including reduced levels of certain immunoglobulins and altered lymphocyte ratios, though results were not statistically significant.
  • Further studies are being conducted with more subjects to explore the long-term health risks of toxaphene, particularly its potential impact on offspring exposed in utero.

Article Abstract

Toxaphene in glycerol/corn oil was administered at 1mg/kg body weight/day, 7 days/week in gelatin capsules to four healthy young adult cynomolgus (Macaca fascicularis) (two male and two female) monkeys for 52 weeks. Control monkeys ingested glycerol/corn oil only. Testing for immune effects was initiated at 34 weeks of treatment. Results included: reduced anti-sheep red blood cell (SRBC) titres for immunoglobulins (Ig) M and G; increased IgG titres to pneumococcal antigens, but not to the tetanus toxoid antigen; reduced T-helper/inducer mean lymphocyte numbers and the mean T-helper/inducer:T-suppressor/cytotoxic cell ratio and reduced respiratory burst activity in peripheral blood monocytes and granulocytes, albeit no changes on the phagocytic activity of these cells were detected. The above noted effects although not statistically significant (P0.05) suggest that chronic exposure to low levels of toxaphene may be immunosuppressive in cynomolgus monkeys and may pose a hazard to human health. To advance our understanding of the degree of hazard that toxaphene may pose to human health, we have undertaken additional chronic studies with a larger number of animals. Particular attention is focused on determining the potential immunotoxic effects of toxaphene in offspring following in utero exposure.

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Source
http://dx.doi.org/10.1016/s0278-6915(99)00122-2DOI Listing

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