Immunosuppression without liver induction by subchronic exposure to 2,7-dichlorodibenzo-p-dioxin in adult female B6C3F1 mice

Toxicol Appl Pharmacol. 1986 May;83(3):445-55. doi: 10.1016/0041-008x(86)90227-9.

Abstract

The overall objective of this investigation was to begin to characterize the structure-activity relationship associated with dioxin-induced suppression of humoral immunity. Subchronic exposure (14 days) to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), the prototype of the class, produced a suppression of the antibody responses to both sheep erythrocytes, a T-dependent antigen, and dinitrophenyl-Ficoll, a T-independent antigen. Surprisingly, similar results were observed with 2,7-dichlorodibenzo-p-dioxin (DCDD), a dioxin congener lacking affinity for the Ah receptor. In contrast, subchronic exposure to octachlorodibenzo-p-dioxin (OCDD), another dioxin congener without affinity for the Ah receptor, was devoid of activity. Subchronic exposure to 2,3,7,8-TCDD, but not 2,7-DCDD, produced an induction of several liver parameters including: liver weight, amount of microsomal protein, amount of cytochrome P-450, activity of aminopyrine-N-demethylase and activity of aryl hydrocarbon hydroxylase. Subchronic exposure to 2,3,7,8-TCDD or 2,7-DCDD produced no marked changes in thymus weight. Acute exposure to 2,3,7,8-TCDD also produced suppression of the antibody response in the absence of effects on the thymus.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibody Formation / drug effects*
  • Biotransformation
  • Body Weight / drug effects
  • Dioxins / metabolism
  • Dioxins / toxicity*
  • Erythrocytes / immunology
  • Female
  • Immunoglobulin M / biosynthesis
  • Lipopolysaccharides / immunology
  • Liver / drug effects
  • Mice
  • Microsomes, Liver / metabolism*
  • Organ Size / drug effects
  • Polychlorinated Dibenzodioxins / toxicity
  • Sheep
  • Spleen / immunology
  • T-Lymphocytes / immunology
  • Thymus Gland / drug effects

Substances

  • Dioxins
  • Immunoglobulin M
  • Lipopolysaccharides
  • Polychlorinated Dibenzodioxins
  • 2,7-dichlorodibenzo-4-dioxin