Literature DB >> 10413190

Persistent suppression of delayed-type hypersensitivity in adult F344 rats after perinatal exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin.

B C Gehrs1, R J Smialowicz.   

Abstract

Recently we observed a suppressed delayed-type hypersensitivity (DTH) response to bovine serum albumin (BSA) in the 4-5-month-old offspring of F344 rat dams receiving as little as 1.0 microg 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)/kg on gestational day (GD) 14. This study was designed to characterize better this suppression of the DTH response. First, the persistence of the DTH suppression was determined by measuring the DTH response to BSA in the offspring of dams dosed orally with 3.0 microg TCDD/kg on GD14 as well as in age-matched controls at 4, 8, 12 and 19 months of age. TCDD significantly suppressed the males' DTH response through 19 months of age. While the females' DTH response was reduced at 8, 12 and 19 months, significant suppression was observed only at 4 months of age. Secondly, the lowest maternal dose of TCDD that produced DTH suppression was determined by measuring the DTH response to BSA in the 4- and 14-month-old offspring of dams dosed orally with 0, 0.1, 0.3 or 1.0 microg TCDD/kg on GD14. In the males, suppression was observed at a maternal dose as low as 0.1 microg TCDD/kg at 14 months of age, while a maternal dose of 0.3 microg TCDD/kg was necessary to cause suppression in the 14-month-old females. Both males and females were more sensitive to the suppression at 14 months of age than at 4 months of age. Lastly, the DTH response to a second antigen was examined by measuring the DTH response to either BSA or keyhole limpet hemocyanin (KLH) in the 5- or 4-month-old male offspring, respectively, of dams dosed orally with either 0 or 3.0 microg TCDD/kg on GD14. The DTH response to both antigens was suppressed significantly. Phenotypic analysis was performed on thymus and lymph node suspensions. Significant effects in the thymus included an increased percentage of gammadelta TCR+ cells and a decreased percentage of gammadelta TCR+/CD4- CD8- and MHCI- MHCII- cells. In the popliteal lymph node draining the BSA-injected footpad, there was a decreased percentage of gammadelta TCR+ and MHCI- MHCII- cells and an increased percentage of MHCI+ cells. In conclusion, the suppression of the DTH response associated with perinatal TCDD exposure is persistent through late adulthood, occurs at a low dose (i.e. 0.1 microg TCDD/kg) to the dam, and is more pronounced in males than females. While phenotypic analysis identified differences in subsets of thymocytes and lymph node cells between control and TCDD exposed offspring, no clear correlations were established between altered subpopulations and suppressed DTH responses.

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Year:  1999        PMID: 10413190     DOI: 10.1016/s0300-483x(99)00024-4

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  13 in total

1.  Prenatal TCDD in mice increases adult autoimmunity.

Authors:  Steven D Holladay; Amjad Mustafa; Robert M Gogal
Journal:  Reprod Toxicol       Date:  2010-08-20       Impact factor: 3.143

2.  The aryl hydrocarbon receptor affects distinct tissue compartments during ontogeny of the immune system.

Authors:  Jason P Hogaboam; Amanda J Moore; B Paige Lawrence
Journal:  Toxicol Sci       Date:  2007-11-17       Impact factor: 4.849

3.  Gestational exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin disrupts B-cell lymphopoiesis and exacerbates autoimmune disease in 24-week-old SNF1 mice.

Authors:  Amjad Mustafa; Steven D Holladay; Sharon Witonsky; Kurt Zimmerman; Christopher M Reilly; D Phillip Sponenberg; Danielle A Weinstein; Ebru Karpuzoglu; Robert M Gogal
Journal:  Toxicol Sci       Date:  2009-08-10       Impact factor: 4.849

Review 4.  Environmental toxicants and the developing immune system: a missing link in the global battle against infectious disease?

Authors:  Bethany Winans; Michael C Humble; B Paige Lawrence
Journal:  Reprod Toxicol       Date:  2010-09-22       Impact factor: 3.143

5.  Developmental exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin alters postnatal T cell phenotypes and T cell function and exacerbates autoimmune lupus in 24-week-old SNF1 mice.

Authors:  Amjad Mustafa; Steven D Holladay; Matthew Goff; Sharon Witonsky; Richard Kerr; Danielle A Weinstein; Ebru Karpuzoglu-Belgin; Robert M Gogal
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-10

6.  An enhanced postnatal autoimmune profile in 24 week-old C57BL/6 mice developmentally exposed to TCDD.

Authors:  A Mustafa; S D Holladay; M Goff; S G Witonsky; R Kerr; C M Reilly; D P Sponenberg; R M Gogal
Journal:  Toxicol Appl Pharmacol       Date:  2008-04-30       Impact factor: 4.219

7.  Evaluation of the potential sensitization of chlorogenic Acid: a meta-analysis.

Authors:  Mingbao Lin; Wan Gong; Qian Chen; Lijuan Sun; Yingchao Wang; Xiaohui Fan
Journal:  Evid Based Complement Alternat Med       Date:  2013-05-16       Impact factor: 2.629

8.  Consensus workshop on methods to evaluate developmental immunotoxicity.

Authors:  Michael I Luster; Jack H Dean; Dori R Germolec
Journal:  Environ Health Perspect       Date:  2003-04       Impact factor: 9.031

Review 9.  Development of the murine and human immune system: differential effects of immunotoxicants depend on time of exposure.

Authors:  S D Holladay; R J Smialowicz
Journal:  Environ Health Perspect       Date:  2000-06       Impact factor: 9.031

Review 10.  Perinatal immunotoxicity: why adult exposure assessment fails to predict risk.

Authors:  Rodney R Dietert; Michael S Piepenbrink
Journal:  Environ Health Perspect       Date:  2006-04       Impact factor: 9.031

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