Literature DB >> 1949050

A review of 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced changes in immunocompetence: 1991 update.

M P Holsapple1, N K Snyder, S C Wood, D L Morris.   

Abstract

2,3,7,8-tetrachlorodibenzo-p-dioxin, more popularly called dioxin or TCDD and referred to in this review as 2,3,7,8-TCDD, is considered the prototype of the polychlorinated dibenzo-p-dioxins (PCDD). The PCDD are true contaminants and are formed primarily as byproducts in the manufacture of materials requiring the use of chlorinated phenols and during the combustion of chlorinated chemical products. From an environmental perspective, the PCDD have been most closely associated with the use of a number of phenolic herbicides, including Agent Orange, which is a 1:1 mixture of the butyl esters of 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). 2,3,7,8-TCDD and related PCDD are not produced commercially except in small amounts for research purposes and to date, have no known human benefit. 2,3,7,8-TCDD has been demonstrated to be the most potent and the most biologically active congener among the halogenated aromatic hydrocarbons (HAH), which include polychlorinated and polybrominated biphenyls (PCB and PBB, respectively) and the polychlorinated dibenzofurans (PCDF), in addition to the PCDD. An updated review on the effects of 2,3,7,8-TCDD on immunocompetence is timely from a number of perspectives. First, effects on immune function have been demonstrated to be among the earliest and most sensitive indicators of 2,3,7,8-TCDD-induced toxicity. Second, recent evidence indicates that exposure to 2,3,7,8-TCDD causes changes in innate immunity in addition to the changes in acquired immunity (i.e., which include effects on both cell-mediated and humoral immunity) previously shown to be associated with this chemical. Third, effects on immune function are almost universally observed among the animal species in which it has been evaluated, including some non-human primates. Fourth, effects of 2,3,7,8-TCDD on specific indicators of immune function have been correlated with changes in host resistance capabilities, which are often considered to be more holistic indicators of immunocompetence. Fifth, there are several reports which describe possible effects of 2,3,7,8-TCDD and related compounds (i.e., primarily PBB and PCB) on immune function in humans. It is important to emphasize at the onset that these studies have triggered much controversy, both political and scientific. However, it is equally important to speculate that at least part of the controversy associated with man's sensitivity to the immunological effects of 2,3,7,8-TCDD may be that the most appropriate approaches have heretofore not been applied. This possibility is discussed further in this review.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1949050     DOI: 10.1016/0300-483x(91)90184-3

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


  25 in total

1.  2,3,7,8-tetrachlorodibenzo-p-dioxin-mediated suppression of toll-like receptor stimulated B-lymphocyte activation and initiation of plasmacytic differentiation.

Authors:  Colin M North; Robert B Crawford; Haitian Lu; Norbert E Kaminski
Journal:  Toxicol Sci       Date:  2010-03-26       Impact factor: 4.849

2.  An integrated genomic analysis of aryl hydrocarbon receptor-mediated inhibition of B-cell differentiation.

Authors:  K Nadira De Abrew; Norbert E Kaminski; Russell S Thomas
Journal:  Toxicol Sci       Date:  2010-09-06       Impact factor: 4.849

3.  A single mid-gestation exposure to TCDD yields a postnatal autoimmune signature, differing by sex, in early geriatric C57BL/6 mice.

Authors:  A Mustafa; S D Holladay; S Witonsky; D P Sponenberg; E Karpuzoglu; R M Gogal
Journal:  Toxicology       Date:  2011-09-06       Impact factor: 4.221

4.  Impaired cellular immune response in harbour seals (Phoca vitulina) feeding on environmentally contaminated herring.

Authors:  R L De Swart; P S Ross; H H Timmerman; H W Vos; P J Reijnders; J G Vos; A D Osterhaus
Journal:  Clin Exp Immunol       Date:  1995-09       Impact factor: 4.330

5.  Generation of alphabeta T-cell receptor+ CD4- CD8+ cells in major histocompatibility complex class I-deficient mice upon activation of the aryl hydrocarbon receptor by 2,3,7,8-tetrachlorodibenzo-p-dioxin.

Authors:  S Kronenberg; Z Lai; C Esser
Journal:  Immunology       Date:  2000-06       Impact factor: 7.397

6.  Parameters of immunological competence in subjects with high consumption of fish contaminated with persistent organochlorine compounds.

Authors:  B G Svensson; T Hallberg; A Nilsson; A Schütz; L Hagmar
Journal:  Int Arch Occup Environ Health       Date:  1994       Impact factor: 3.015

7.  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

8.  TCDD-mediated suppression of the in vitro anti-sheep erythrocyte IgM antibody forming cell response is reversed by interferon-gamma.

Authors:  Colin M North; Byung-Sam Kim; Neil Snyder; Robert B Crawford; Michael P Holsapple; Norbert E Kaminski
Journal:  Toxicol Sci       Date:  2008-10-22       Impact factor: 4.849

9.  Simultaneous in vivo time course and dose response evaluation for TCDD-induced impairment of the LPS-stimulated primary IgM response.

Authors:  Colin M North; Robert B Crawford; Haitian Lu; Norbert E Kaminski
Journal:  Toxicol Sci       Date:  2009-08-12       Impact factor: 4.849

10.  Immunological markers among workers exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin.

Authors:  W Halperin; R Vogt; M H Sweeney; G Shopp; M Fingerhut; M Petersen
Journal:  Occup Environ Med       Date:  1998-11       Impact factor: 4.402

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.