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Biologic Markers in Immunotoxicology (1992)
Commission on Life Sciences (CLS)

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Biologic Markers in Immunotoxicology

TABLE 5-3 Classes and Examples of Chemicals Causing Immunologic Changes

Class

Examples

Polyhalogenated aromatic hydrocarbons

TCDD, PBBs, PCDF, PCBs, hexachlorobenzene

Metals

Lead, calcium, arsenic, methyl mercury

Aromatic hydrocarbvons (solvents)

Benzene, toluene

Polycyclic aromatic hydrocarbons

DMBA, B[a]P, MCA

Pesticides

Trimethyl phosphorothioate, carbofuran, chlordane, malathion

Organotins

TBTO

Aromatic amines

Benzidene, acetyl aminofluorene

Oxidant gases

Nitrogen dioxide, ozone, sulfur, dioxide

Particles

Silica, asbestos

Natural products

Selected vitamins, antibiotics, vinca alkaloids, estrogen, plant alkaloids, mycotoxins

Drugs of abuse

Ethanol, cannabinoids, cocaine, opioids

Therapeutic drugs

Diphenylhydantoin, lithium

Others

Nitrosamine, BHA

Abbreviations: TCDD, 2,3,7,8-tetrachlorodibenzo-p-dioxin; PBBs, polybrominated biphenyls; PCDF, polychlorinated dibenzofuran; PCBs, polychlorinated biphenyls; DMBA, dimethylbenzanthracene; B[a]P, benzo[a]pyrene; MCA, methylcholanthrene; TBTO, bis(tris-n-butylin)oxide; BHA, butylated hydroxyanisole.

agents or tumor cells. Animal studies, primarily those which use rodents, have provided a large information base about potentially immunotoxic chemicals, suggestive evidence of the mechanisms for their effects, and an appreciation that the immune system is susceptible to chemical injury. The susceptibility of the immune system is due as much to the general properties of a chemical (e.g., its reactivity to macromolecules) as it is to the complex nature of the immune system. Because the cellular events responsible for immune processes also are involved in embryogenesis, many immunosuppressive xenobiotics would be expected to be developmental toxicants.

To date, animal data have not been used to any significant extent in the assessment of human risk resulting from exposure to immunosuppressive environmental pollutants. Extrapolating short-term, high-dose animal studies to chronic low-dose human exposure

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