Autoantibodies Associated with Volatile Anesthetic Hepatitis Found in the Sera of a Large Cohort of Pediatric Anesthesiologists
- 1 February 2002
- journal article
- pediatric anesthesia
- Published by Wolters Kluwer Health in Anesthesia & Analgesia
- Vol. 94 (2) , 243-249
- https://doi.org/10.1097/00000539-200202000-00003
Abstract
Anesthetic-induced hepatitis is thought to have an immune-mediated basis, in part because many patients who develop hepatitis have serum autoantibodies that react with specific hepatic proteins. The present study shows that pediatric anesthesiologists also have these serum autoantibodies. Moreover, levels of these autoantibodies are higher than those of general anesthesiologists. We collected sera from 105 pediatric and 53 general anesthesiologists (including 3 nurse anesthetists), 20 halothane hepatitis patients, and 20 control individuals who were never exposed to inhaled anesthetics. Serum cytochrome P450 2E1 (P450 2E1) and 58-kd hepatic endoplasmic reticulum protein (ERp58) autoantibodies were measured by enzyme-linked immunosorbent assays. Positive values were 2 sd above median control values. Two multiple regression models were constructed. Pediatric anesthesiologists, like halothane hepatitis patients, had higher serum autoantibody levels of ERp58 and P450 2E1 than general anesthesiologists and controls, which was possibly because of their increased occupational exposures to anesthetics. Female anesthesiologists had higher levels of ERp58 autoantibodies than male anesthesiologists, whereas female pediatric anesthesiologists had higher levels of P450 2E1 autoantibodies than all other anesthesiologists. One female pediatric anesthesiologist had symptoms of hepatic injury. Because most anesthesiologists do not develop volatile anesthetic-induced hepatic injury, the findings suggest that pathogenic ERp58 and P450 2E1 autoantibodies may not directly cause volatile anesthetic hepatitis. Female anesthesiologists have high levels of these autoantibodies; however, the majority of these individuals do not develop hepatitis, suggesting that autoantibodies may not have a pathological role in volatile anesthetic-induced hepatitis.Keywords
This publication has 12 references indexed in Scilit:
- Immunochemical Evidence against the Involvement of Cysteine Conjugate β-lyase in Compound A Nephrotoxicity in RatsAnesthesiology, 1999
- Biotransformation of Halothane, Enflurane, Isoflurane, and Desflurane to Trifluoroacetylated Liver ProteinsAnesthesia & Analgesia, 1997
- Human Cytochrome P450 2E1 Is a Major Autoantigen Associated with Halothane HepatitisChemical Research in Toxicology, 1996
- cDNA Cloning and Baculovirus Expression of the Human Liver Endoplasmic Reticulum P58: Characterization as a Protein Disulfide Isomerase Isoform, but Not as a Protease or a Carnitine AcyltransferaseArchives of Biochemistry and Biophysics, 1995
- Association of anti-58 kDa endoplasmic reticulum antibodies with halothane hepatitisBiochemical Pharmacology, 1993
- A metabolite of halothane covalently binds to an endoplasmic reticulum protein that is highly homologous to phosphatidylinositol-specific phospholipase C-α but has no activityBiochemical and Biophysical Research Communications, 1991
- Antibody Assays for the Detection of Patients Sensitized to HalothaneAnesthesia & Analgesia, 1990
- HEPATIC DAMAGE AFTER EXPOSURE TO HALOTHANE IN MEDICAL PERSONNELBritish Journal of Anaesthesia, 1981
- Chronic Exposure to Anesthetic Gases in the Operating RoomAnesthesiology, 1971
- Recurrent Hepatitis Attributable to Halothane Sensitization in an AnesthetistNew England Journal of Medicine, 1969