PMID- 1910589 OWN - NLM STAT- MEDLINE DCOM- 19911121 LR - 20180608 IS - 0895-3988 (Print) IS - 0895-3988 (Linking) VI - 4 IP - 1-2 DP - 1991 Jun TI - Critical considerations in the immunochemical detection and quantitation of antigenic biomarkers. PG - 113-29 AB - The formation of covalent adducts as a result of the interaction of metabolically activated chemicals with host macromolecules is a common critical event in mutagenic, carcinogenic, and immunologic phenomena. Because of their antigenicity and their immunogenicity, covalent adducts may be detected using sensitive immunochemical techniques. The immunochemical approaches to biomonitoring and molecular dosimetry of DNA damage are particularly attractive because they allow sensitive quantitation of specific DNA adducts present in small samples and do not rely on the use of radiolabeled adducts. Two examples of biomarker immunoassay development are presented: an avidin/biotin-amplified ELISA for the major DNA adduct of the human bladder carcinogen 4-aminobiphenyl (ABP), and a particle concentration fluorescent immunoassay (PCFIA) for the major protein adduct associated with toxicity by the prototype hepatotoxin acetaminophen. The examples illustrate critical steps in the development of biomarker immunoassays which include selection of the relevant adduct, preparation of an appropriate immunogen, immunization, characterization of antisera, and development of application-specific sample processing techniques for biomarker quantitation. Immunochemical procedures may be combined with other analytical techniques to form hybrid systems which take advantage of both the antigenicity and the physical or chemical properties of a biomarker to achieve greater specificity and/or sensitivity. The future usefulness of these new tools of molecular epidemiology will depend on a compound-by-compound validation of methods and critical evaluation of the biologic importance of the particular antigenic biomarker as an indicator of exposure and as an indicator of risk. FAU - Roberts, D W AU - Roberts DW AD - Division of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, Arkansas 72079-9502. FAU - Benson, R W AU - Benson RW FAU - Hinson, J A AU - Hinson JA FAU - Kadlubar, F F AU - Kadlubar FF LA - eng PT - Journal Article PT - Review PL - China TA - Biomed Environ Sci JT - Biomedical and environmental sciences : BES JID - 8909524 RN - 0 (Aminobiphenyl Compounds) RN - 0 (Antigens) RN - 0 (Biomarkers) RN - 0 (Carcinogens) RN - 16054949HJ (4-biphenylamine) RN - 362O9ITL9D (Acetaminophen) SB - IM MH - Acetaminophen/metabolism/toxicity MH - Aminobiphenyl Compounds/metabolism/toxicity MH - Antigens/*analysis MH - *Biomarkers MH - Carcinogens/metabolism MH - DNA Damage MH - Humans MH - Immunoassay MH - Immunochemistry/*methods MH - Sensitivity and Specificity RF - 43 EDAT- 1991/06/01 00:00 MHDA- 1991/06/01 00:01 CRDT- 1991/06/01 00:00 PHST- 1991/06/01 00:00 [pubmed] PHST- 1991/06/01 00:01 [medline] PHST- 1991/06/01 00:00 [entrez] PST - ppublish SO - Biomed Environ Sci. 1991 Jun;4(1-2):113-29.