TY - JOUR
T1 - Serum IgE and IgG to formaldehyde-human serum albumin
T2 - Lack of relation to gaseous formaldehyde exposure and symptoms
AU - Dykewicz, Mark S.
AU - Patterson, Roy
AU - Cugell, David W.
AU - Harris, Kathleen E.
AU - Wu, Anna Fang
N1 - Funding Information:
From the Sections of Allergy-Immunology and **Pulmonary Med-icine, Department of Medicine, Northwestern University Medi-cal School, and ***Employee Health Service, Northwestern Me-morial Hospital, Chicago, Ill. Supported by United States Public Health Service Grant AI 11403 and the Ernest S. Barley Grant. Received for publication March 19, 1990. Revised Aug. 3, 1990. Accepted for publication Aug. 14, 1990. Reprint requests: Roy Patterson, MD, Northwestern University Medical School, 303 E. Chicago Ave., Chicago, IL 60611. *Dr. Mark S. Dykewicz was supported by a grant from the RJR Nabisco Research Scholars Award Program; present address: Di-vision of Allergy-Immunology, Department of Internal Medicine, St. Louis University School of Medicine, St. Louis, MO 63104. l/1/24498
PY - 1991/1
Y1 - 1991/1
N2 - Fifty-five subjects were studied to determine if the presence of IgE or IgG antibodies to formaldehyde (F)-human serum albumin (HSA) was associated with exposure to gaseous F or with respiratory or conjunctival symptoms from such exposure. The study population included cohorts exposed to F in the workplace, smokers, and normal subjects. IgE antibody specific for F-HSA was detected by ELISA in three subjects; immediate-type skin testing was negative in two of these subjects, and not interpretable because of dermatographism in one subject. One of these subjects had a history of respiratory symptoms when the subject was working in a histology laboratory that contained ambient F and xylene; a respiratory challenge with F at concentrations of up to 2 ppm failed to produce respiratory symptoms or significant changes in pulmonary function. Serum from the three subjects with IgE to F-HSA by ELISA failed to passively transfer skin reactivity to F-HSA to rhesus monkey recipients. These three subjects and two other subjects had IgG to F-HSA by ELISA, although this was of generally low titer. We could not define a relationship between the presence of antibodies and (1) a history of F exposure or (2) a history of adverse respiratory or conjunctival symptoms from F. This study is a continuum of 5 years of study in our laboratory attempting to define allergy to gaseous F, and the current study does not support an immunologic basis for respiratory or conjunctival symptoms from gaseous F exposure. Based on the findings of this and our other studies, it is possible that clinical IgE-mediated allergy to gaseous F does not exist, or if it does exist, it is extremely rare.
AB - Fifty-five subjects were studied to determine if the presence of IgE or IgG antibodies to formaldehyde (F)-human serum albumin (HSA) was associated with exposure to gaseous F or with respiratory or conjunctival symptoms from such exposure. The study population included cohorts exposed to F in the workplace, smokers, and normal subjects. IgE antibody specific for F-HSA was detected by ELISA in three subjects; immediate-type skin testing was negative in two of these subjects, and not interpretable because of dermatographism in one subject. One of these subjects had a history of respiratory symptoms when the subject was working in a histology laboratory that contained ambient F and xylene; a respiratory challenge with F at concentrations of up to 2 ppm failed to produce respiratory symptoms or significant changes in pulmonary function. Serum from the three subjects with IgE to F-HSA by ELISA failed to passively transfer skin reactivity to F-HSA to rhesus monkey recipients. These three subjects and two other subjects had IgG to F-HSA by ELISA, although this was of generally low titer. We could not define a relationship between the presence of antibodies and (1) a history of F exposure or (2) a history of adverse respiratory or conjunctival symptoms from F. This study is a continuum of 5 years of study in our laboratory attempting to define allergy to gaseous F, and the current study does not support an immunologic basis for respiratory or conjunctival symptoms from gaseous F exposure. Based on the findings of this and our other studies, it is possible that clinical IgE-mediated allergy to gaseous F does not exist, or if it does exist, it is extremely rare.
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U2 - 10.1016/0091-6749(91)90212-7
DO - 10.1016/0091-6749(91)90212-7
M3 - Article
C2 - 1991923
AN - SCOPUS:0025806446
SN - 0091-6749
VL - 87
SP - 48
EP - 57
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 1 PART 1
ER -