1985
DOI: 10.1016/0300-483x(85)90033-2
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Humoral immunotoxicity of polychlorinated diphenyl ethers, phenoxyphenols, dioxins and furans present as contaminants of technical grade pentachlorophenol

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Cited by 68 publications
(26 citation statements)
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“…Two lines of evidence support this conclusion: comparative studies using PCDD, PCDF, and PCB congeners show that potency to cause immune suppression correlates with the binding affinity for the AhR (25)(26)(27)(28)(29); and studies using mice with a defined Ah genotype show that mice with high affinity AhR (e.g., Ahbb C57BI/6 mice) are more sensitive to immune suppression by these compounds than mice with lower affinity AhR (e.g., Ahdd DBA/2 mice or Ahdd congenic C57BI/6 mice) (8,25,26,29). AhR-dependent responses include suppression of the T-cell-dependent antibody response to SRBC (8,(25)(26)(27)(28)30,31), suppression of the T-cell-independent antibody response to trinitrophenyl-lipopolysaccharide (8), suppression of the cytotoxic T lymphocyte (CTL) response to allogeneic tumor cells (29,32) bone marrow toxicity (33), and suppression of the cytotoxic responses of activated neutrophils (34 however, the specific cellular defects induced by TCDD have not been fully elucidated despite considerable research. One of the problems has been a difficulty in demonstrating direct effects of TCDD on in vitro responses of lymphoid cells (35,36).…”
Section: Immunotoxicity Studies Laboratory Animal Studiesmentioning
confidence: 61%
“…Two lines of evidence support this conclusion: comparative studies using PCDD, PCDF, and PCB congeners show that potency to cause immune suppression correlates with the binding affinity for the AhR (25)(26)(27)(28)(29); and studies using mice with a defined Ah genotype show that mice with high affinity AhR (e.g., Ahbb C57BI/6 mice) are more sensitive to immune suppression by these compounds than mice with lower affinity AhR (e.g., Ahdd DBA/2 mice or Ahdd congenic C57BI/6 mice) (8,25,26,29). AhR-dependent responses include suppression of the T-cell-dependent antibody response to SRBC (8,(25)(26)(27)(28)30,31), suppression of the T-cell-independent antibody response to trinitrophenyl-lipopolysaccharide (8), suppression of the cytotoxic T lymphocyte (CTL) response to allogeneic tumor cells (29,32) bone marrow toxicity (33), and suppression of the cytotoxic responses of activated neutrophils (34 however, the specific cellular defects induced by TCDD have not been fully elucidated despite considerable research. One of the problems has been a difficulty in demonstrating direct effects of TCDD on in vitro responses of lymphoid cells (35,36).…”
Section: Immunotoxicity Studies Laboratory Animal Studiesmentioning
confidence: 61%
“…It was concluded that T-cells, NK cells, and macrophages were relatively resistant to T-PCP, in contrast to the marked sensitivity of elements of the humoral immune response. Several contaminant fractions and purified isomers from T-PCP were analyzed for their humoral immunosuppressive effect (Kerkvliet et al, 1985b). The 1,2,3,6,7,1,2,3,4,6,7,and 1,2,3,4,6,7, this and other evidence was presented for the role of toxic Ah-interactive dioxin and furan contaminants in T-PCP mediated immunotoxicity.…”
Section: ~0 260mentioning
confidence: 97%
“…It is a well-known uncoupler of mitochondrial oxidative phosphorylation and modulator of cytochrome P-450 (Arrhenius et al, 1977), which produces numerous physiological 255 effects including immunotoxicity. Analytical grade (pure) PCP (A-PCP) is reported to have little immunotoxicity in laboratory rodents, whereas technical grade PCP (T-PCP) shows immunosuppressive activity, probably due to the presence of contaminants such as 1,2,3,6,7,8-hexachlorodibenzo-p-dioxin (HCDD) (Holsapple et al, 1984(Holsapple et al, , 1987Kerkvliet et al, 1985b).However, exposure of the mollusc Mercenaria to analytical grade PCP produced an impairment in the ability of the phagocytic hemocytes to destroy bacteria in vivo or in vitro (Anderson et al, 1981;Anderson, 1988). In the current study with medaka, the effects of both A-PCP and T-PCP on phagocyte-mediated CL are considered.…”
mentioning
confidence: 99%
“…Nevertheless, prenatal effects on the thymus and/or T-cell-mediated immunity may be critical. The immunotoxic effects of TCDD have been shown to be mediated by binding to the Ah receptor, based on structure/activity studies and use of mice genetically different in their responsiveness to TCDD (6)(7)(8)(9). The cellular targets of TCDD appear to be multiple, as suggested by the different assays and end points that have been assessed.…”
Section: Introductionmentioning
confidence: 99%