The weeks shown in color represent the start and end points of chemical exposure for each study.
Study Results | Study Details | References |
Results for Dioxin (TCDD)Decreased relative weight of thymus in F3 generation at 0.01 μg/kg/day |
Subjects: Sprague-Dawley rats Chemical: Dioxin (TCDD) Low doses tested: 0.001 or 0.01 μg/kg bw/day Other doses tested: 0.1 μg/kg bw/day Route of administration: delivered daily in feed Exposure duration: 90 days prior to mating – fed daily (comparable to human prenatal development from approximately day 1 of week 1 to beyond birth) Age of measurement: 90 days prior to mating through 396 days of age |
Reference [PubMed Link] Murray FJ, Smith FA, Nitschke KD, Humiston CG, Kociba RJ, Schwetz BA. 1979 Sep 15. Three-generation reproduction study of rats given 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in the diet. Toxicol Appl Pharmacol 50(2):241-52. |
Study Results | Study Details | References |
Results for Dioxin (TCDD)Decreased number of immunodominant viral peptide NP366-372/Db + CD8+ T-cells nine days after infection with 120 HAU of influenza A virus in mediastinal lymph nodes (MLN) for gestational plus lactational, and lactational only TCDD exposure; decreased number of cytotoxic T lymphocyte effector cells (CTLe) defined phenotypically as CD44hi CD621lo CD8+ and expansion of NP366-372/Db + CD8+ T-cells in MLN in recipients that had been lethally irradiated and received bone marrow cells from offspring of TCDD treated dams |
Subjects: C57BL/6 mice Chemical: Dioxin (TCDD) Low doses tested: 1.0 μg/kg bw on gestational days 0, 7, and 14 and at 2 days of age Route of administration: dissolved in peanut oil and delivered through gavage Exposure duration: gestational day 0 (cross-fostered at 2 days of age) – last dose at 2 days of age (comparable to human prenatal development from approximately day 1 of week 1 to beyond birth) Age of measurement: eight through 10 weeks of age |
Reference [PubMed Link] Hogaboam JP, Moore AJ, Lawrence BP. 2008 Mar. The aryl hydrocarbon receptor affects distinct tissue compartments during ontogeny of the immune system. Toxicol Sci 102(1):160-70. |