The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Immune-mediated drug-induced liver disease
Abstract
Drug-induced immune-mediated hepatic injury is an adverse immune response against the liver that results in a disease with hepatitic, cholestatic, or mixed clinical features. Drugs such as halothane, tienilic acid, dihydralazine, and anticonvulsants trigger a hepatitic reaction, and drugs such as chlorpromazine, erythromycins, amoxicillin-calvulanic acid, sulfonamides and sulindac trigger a cholestatic or mixed reaction. Unstable metabolites derived from the metabolism of the drug may bind to cellular proteins or macromolecules, leading to a direct toxic effect on hepatocytes. Protein adducts formed in the metabolism of the drug may be recognized by the immune system as neoantigens. Immunocyte activation may then generate autoantibodies and cell-mediated immune responses, which in turn damage the hepatocytes. Cytochromes 450 are the major oxidative catalysts in drug metabolism, and they can form a neoantigen by covalently binding with the drug metabolite that they produce. Autoantibodies that develop are selectively directed against the particular cytochrome isoenzyme that metabolized the parent drug. The hapten hypothesis proposes that the drug metabolite can act as a hapten and can modify the self of the individual by covalently binding to proteins. The danger hypothesis proposes that the immune system only responds to a foreign antigen if the antigen is associated with a danger signal, such as cell stress or cell death. Most clinically overt adverse hepatic events associat…
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The term "immune-mediated DILI" is associated with many drugs that are not associated with well recognised autoimmune features.
“The term “immune-mediated DILI” is also associated with many drugs that are not associated with well recognised autoimmune features.”
From Nomenclature, diagnosis and management of drug-induced autoimmune-like hepatitis (DI-ALH): An expert opinion meeting report (2023) · cites this paper as [22]
DI-ALH presents as a self-limited phenotype that resolves or becomes quiescent when the drug is removed, but in some cases liver injury progresses to chronicity and a self-perpetuating autoimmune liver disease ensues.
“Thus, DI-AHL presents as a “self-limited” phenotype that resolves or becomes quiescent when the drug is removed, but in some cases, liver injury does progress to chronicity and a “self-perpetuating” autoimmune liver disease ensues (Fig. 2).22,51,52”
From Nomenclature, diagnosis and management of drug-induced autoimmune-like hepatitis (DI-ALH): An expert opinion meeting report (2023) · cites this paper as [22]
Citations
Cites
Doherty, D. G., Norris, S., Madrigal-Estebas, L., McEntee, G., Traynor, O., Hegarty, J. E., & O’Farrelly, C. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.4.2314 · Cited by 350
Role of Drug Disposition in Drug Hypersensitivity: A Chemical, Molecular, and Clinical Perspective
Park, B. K., Pirmohamed, M., & Kitteringham, N. R. (1998) · Chemical Research in Toxicology · doi:10.1021/tx980058f · Cited by 267
Kim, H.-J., Kim, B.-H., Han, Y.-S., Yang, I., Kim, K.-J., Dong, S.-H., Kim, H.-J., Chang, Y.-W., Lee, J.-I., & Chang, R. (2001) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2001.03469.x · Cited by 99
Flagged first, then by citations
Research works printed but not linked: 94
- Obermayer-Straub, 2000, Autoimmune hepatitis, J Hepatol, 32, 181, 10.1016/S0168-8278(00)80425-0 · DOI
- Manns, 1997, Cytochrome P450 and uridine triphosphate-glucuronosyltransferase: model autoantigens to study drug-induced, virus-induced, and autoimmune liver disease, Hepatology, 26, 1054, 10.1002/hep.510260438 · DOI
- Robin, 1997, Plasma membrane cytochromes P450 as neoantigens and autoimmune targets in drug-induced hepatitis, J Hepatol, 26, 23, 10.1016/S0168-8278(97)82329-X · DOI
- Bissell, 2001, Drug-induced livery injury: mechanisms and test systems, Hepatology, 33, 1009, 10.1053/jhep.2001.23505 · DOI
- Kaplowitz, 2001, Drug-induced liver diseases: implications for drug development and regulation, Drug Saf, 24, 483, 10.2165/00002018-200124070-00001 · DOI
- Beaune, 1997, Immunotoxicity of the liver: adverse reactions to drugs, J Hepatol, 26, 37, 10.1016/S0168-8278(97)80495-3 · DOI
- Knowles, 2000, Idiosyncratic drug reactions: the reactive metabolite syndrome, Lancet, 356, 1587, 10.1016/S0140-6736(00)03137-8 · DOI
- Uetrecht, 1999, New concepts in immunology relevant to idiosyncratic drug reactions: the “danger hypothesis” and innate immune system, Chem Res Toxicol, 12, 387, 10.1021/tx980249i · DOI
- Kitteringham, 1990, Drug-protein conjugation and its immunological consequences, Drug Metabol Rev, 22, 87, 10.3109/03602539008991445 · DOI
- Matzinger, 1994, Tolerance, danger, and the extended family, Annu Rev Immunol, 12, 991, 10.1146/annurev.iy.12.040194.005015 · DOI
- Gordin, 1984, Adverse reactions to trimethoprin-sulfamethoxazole in patients with the acquired immunodeficiency syndrome, Ann Intern Med, 100, 495, 10.7326/0003-4819-100-4-495 · DOI
- Bourdi, 1994, Interactions of dihydralazine with cytochromes P4501A: a possible explanation for the appearance of anti-P4501A2 autoantibodies, Mol Pharmacol, 45, 1287, 10.1016/S0026-895X(25)10602-0 · DOI
- Bourdi, 1990, Anti-liver endoplasmic reticulum autoantibodies are directed against human liver cytochrome P-450 IA2. A specific marker of dihydralazine-induced hepatitis, J Clin Invest, 85, 1967, 10.1172/JCI114660 · DOI
- Beaune, 1994, Autoantibodies against cytochromes P450: role in human diseases, Adv Pharmacol, 30, 199, 10.1016/S1054-3589(08)60175-1 · DOI
- Vergani, 1980, Antibodies to the surface of halothane-altered rabbit hepatocytes in patients with severe halothane-associated hepatitis, N Engl J Med, 303, 66, 10.1056/NEJM198007103030202 · DOI
- Eliasson, 1996, Cytochrome P4502E1 is a cell surface autoantigen in halothane hepatitis, Mol Pharmacol, 50, 573, 10.1016/S0026-895X(25)09316-2 · DOI
- Loeper, 1993, Cytochromes P-450 on human hepatocyte plasma membrane. Recognition by several autoantibodies, Gastroenterology, 104, 203, 10.1016/0016-5085(93)90853-5 · DOI
- Loeper, 1990, Presence of functional cytochrome P-450 on isolated rat hepatocyte plasma membrane, Hepatology, 11, 850, 10.1002/hep.1840110521 · DOI
- Robin, 2000, Vesicular transport of newly synthesized cytochromes P4501A to the outside of rat hepatocyte plasma membranes, J Pharmacol Exp Ther, 294, 1063, 10.1016/S0022-3565(24)39172-4 · DOI
- Robin, 1996, Antigenic targets in tienilic acid hepatitis. Both cytochrome P450 2C11 and 2C11-tienilic acid adducts are transported to the plasma membrane of rat hepatocytes and recognized by human sera, J Clin Invest, 98, 1471, 10.1172/JCI118936 · DOI
- Satoh, 1987, An immunochemical approach to investigating the mechanism of halothane-induced hepatotoxicity, Prog Drug Metab, 10, 187
- Sakaguchi, 1984, Signal recognition particle is required for the co-translational insertion of cytochrome P450 into microsomal membranes, Proc Natl Acad Sci USA, 81, 3361, 10.1073/pnas.81.11.3361 · DOI
- Robin, 1995, Cytochrome P4502B follows a vesicular route to the plasma membrane in cultured rat hepatocytes, Gastroenterology, 108, 1110, 10.1016/0016-5085(95)90210-4 · DOI
- Haouzi, 2000, Cytochrome P450-generated reactive metabolites cause mitochondrial permeability transition, caspase activation, and apoptosis in rat hepatocytes, Hepatology, 32, 303, 10.1053/jhep.2000.9034 · DOI
- Yang, 1995, Upregulation of class I major histocompatibility complex antigens by interferon gamma is necessary for T-cell-mediated elimination of recombinant adenovirus-infected hepatocytes in vivo, Proc Natl Acad Sci USA, 92, 7257, 10.1073/pnas.92.16.7257 · DOI
- Neuberger, 1989, Immune mechanism in tienilic acid associated hepatotoxicity, Gut, 30, 515, 10.1136/gut.30.4.515 · DOI
- Kita, 2001, The lymphoid liver: considerations on pathways to autoimmune injury, Gastroenterology, 120, 1485, 10.1053/gast.2001.22441 · DOI
- Abo, 1991, The appearance of T cells bearing self-reactive T cell receptor in the livers of mice injected with bacteria, J Exp Med, 174, 417, 10.1084/jem.174.2.417 · DOI
- Bendelac, 1997, Mouse CD1-specific NK1 T cells: development, specificity, and function, Annu Rev Immunol, 15, 535, 10.1146/annurev.immunol.15.1.535 · DOI
- Crispe, 1996, Strange brew: T cells in the liver, Immunol Today, 17, 522, 10.1016/S0167-5699(96)80906-6 · DOI
- Exley, 1997, Requirements for CD1d recognition by human invariant Vα 24+ CD4− CD8− T cells, J Exp Med, 186, 109, 10.1084/jem.186.1.109 · DOI
- Carnaud, 1999, Cross-talk between cells of the innate immune system: NKT cells rapidly activate NK cells, J Immunol, 163, 4647, 10.4049/jimmunol.163.9.4647 · DOI
- Godfrey, 2000, NKT cells: facts, functions and fallacies, Immunol Today, 21, 573, 10.1016/S0167-5699(00)01735-7 · DOI
- Cui, 1997, Requirement for Vα 14 NKT cells in IL-12-mediated rejection of tumors, Science, 278, 1623, 10.1126/science.278.5343.1623 · DOI
- Kakimi, 2000, Natural killer T cell activation inhibits hepatitis B virus replication In vivo, J Exp Med, 192, 921, 10.1084/jem.192.7.921 · DOI
- Singh, 1999, Activation of NK T cells by CD1d and α-galactosylceramide directs conventional T cells to the acquisition of a Th2 phenotype, J Immunol, 163, 2373, 10.4049/jimmunol.163.5.2373 · DOI
- Toyabe, 1997, Requirement of IL-4 and liver NK1+ T cells for concanavalin A-induced hepatic injury in mice, J Immunol, 159, 1537, 10.4049/jimmunol.159.3.1537 · DOI
- Kharasch, 1996, Identification of the enzyme responsible for oxidative halothane metabolism: implications for prevention of halothane hepatitis, Lancet, 347, 1367, 10.1016/S0140-6736(96)91011-9 · DOI
- Satoh, 1985, Immunological studies on the mechanism of halothane-induced hepatotoxicity: immunohistochemical evidence of trifluoroacetylated hepatocytes, J Pharmaocol Exp Ther, 233, 857, 10.1016/S0022-3565(25)22885-3 · DOI
- Bourdi, 1996, Human cytochrome P450 2E1 is a major autoantigen associated with halothane hepatitis, Chem Res Toxicol, 9, 1159, 10.1021/tx960083q · DOI
- Kitteringham, 1995, Detection of autoantibodies directed against human hepatic endoplasmic-reticulum in sera from patients with halothane-associated hepatitis, Br J Clin Pharmarcol, 40, 379, 10.1111/j.1365-2125.1995.tb04560.x · DOI
- Kenna, 1988, Metabolic basis for a drug hypersensitivity: antibodies in sera from patients with halothane hepatitis recognize liver neoantigens that contain the trifluroracetyl group derived from halothane, J Pharmacol Exp Ther, 245, 1103, 10.1016/S0022-3565(25)24104-0 · DOI
- Kenna, 1997, Immunoallergic drug-induced hepatitis: lessons from halothane, J Hepatol, 26, 5, 10.1016/S0168-8278(97)82327-6 · DOI
- Homberg, 1985, Drug-induced hepatitis associated with anticytoplasmic organelle autoantibodies, Hepatology, 5, 722, 10.1002/hep.1840050504 · DOI
- Homberg, 1984, A new anti-liver-kidney microsome antibody (anti-LKM2) in tienilic acid induced hepatitis, Clin Exp Immunol, 55, 561
- Zimmerman, 1984, Ticrynafen-associated hepatic injury: analysis of 340 cases, Hepatology, 4, 315, 10.1002/hep.1840040223 · DOI
- Beaune, 1987, Human anti-endoplasmic reticulum autoantibodies appearing in a drug-induced hepatitis are directed against a human liver cytochrome P-450 that hydroxylates the drug, Proc Natl Acad Sci USA, 84, 551, 10.1073/pnas.84.2.551 · DOI
- Lecoeur, 1996, Tienilic acid-induced autoimmune hepatitis: anti-liver and-kidney microsomal type 2 autoantibodies recognize a three-site conformational epitope on cytochrome P450 2C9, Mol Pharmacol, 50, 326, 10.1016/S0026-895X(25)09234-X · DOI
- Lecoeur, 1994, Specificity of in vitro covalent binding of tienilic acid metabolites to human liver microsomes in relationship with the type of hepatotoxicity: comparison with two directly hepatotoxic drugs, Chem Res Toxicol, 7, 434, 10.1021/tx00039a023 · DOI
- Lopez Garcia, 1994, Thiophene derivatives as new mechanism-based inhibitors of cytochrome P450: inactivation of yeast-expressed human liver P450 2C9 by tienilic acid, Biochemistry, 33, 166, 10.1021/bi00167a022 · DOI
- Lopez Garcia, 1993, Human-liver cytochromes P-450 expressed in yeast as tools for reactive-metabolite formation studies. Oxidative activation of tienilic acid by cytochromes P-450 2C9 and 2C10, Eur J Biochem, 213, 223, 10.1111/j.1432-1033.1993.tb17752.x · DOI
- Pons, 1991, Detection of human hepatitis anti-liver kidney microsomes (LKM2) autoantibodies on rat liver sections is predominantly due to reactivity with rat liver P-450 IIC11, J Pharmacol Exp Ther, 259, 1328, 10.1016/S0022-3565(25)20545-6 · DOI
- Leeder, 1996, Epitope mapping studies with human anti-cytochrome P450 3A antibodies, Mol Pharmacol, 49, 234, 10.1016/S0026-895X(25)08704-8 · DOI
- Siegmund, 1985, The influence of the acetylator phenotype for the clinical use of dihydralazine, Int J Clin Pharmcol Ther Toxicol, 23, S74
- Bourdi, 1992, Anti-liver microsomes autoantibodies and dihydralazine-induced hepatitis: specificity of autoantibodies and inductive capacity of the drug, Mol Pharmacol, 42, 280, 10.1016/S0026-895X(25)08911-4 · DOI
- Rieder, 1991, Prominence of slow acetylator phenotype among patients with sulfonamide hypersensitivity reactions, Clin Pharmacol Ther, 49, 13, 10.1038/clpt.1991.3 · DOI · Paper page
- Nataf, 1986, A new anti-liver microsome antibody: a specific marker of dihydralazine-induced hepatitis [abstract], Gastroenterology, 90, 1751
- Leeder, 1992, Human anti-cytochrome P450 antibodies in aromatic anticonvulsant-induced hypersensitivity reactions, J Pharmacol Exp Ther, 263, 360, 10.1016/S0022-3565(25)10348-0 · DOI
- Riley, 1993, Human anti-endoplasmic reticulum autoantibodies produced in aromatic anticonvulsant hypersensitivity reactions recognise rodent CYP3A proteins and a similarly regulated human P450 enzyme(s), Biochem Biophys Res Commun, 191, 32, 10.1006/bbrc.1993.1180 · DOI
- Leeder, 1998, Non-monooxygenase cytochromes P450 as potential human autoantigens in anticonvulsant hypersensitivity reactions, Pharmacogenetics, 8, 211, 10.1097/00008571-199806000-00004 · DOI
- Gennis, 1991, Familial occurrence of hypersensitivity to phenytoin, Am J Med, 91, 631, 10.1016/0002-9343(91)90216-K · DOI
- Bhat, 1998, Minocycline-induced hepatitis with autoimmune features and neutropenia, Clin Gastroenterol, 27, 74, 10.1097/00004836-199807000-00016 · DOI
- Goldstein, 2000, Minocycline as a cause of drug-induced autoimmune hepatitis. Report of four cases and comparison with autoimmune hepatitis, Am J Clin Pathol, 114, 591, 10.1309/KV2J-VX6Q-L95V-VDE4 · DOI
- Lawrenson, 2000, Liver damage associated with minocycline use in acne: a systematic review of published literature and pharmacovigilance data, Drug Safety, 23, 333, 10.2165/00002018-200023040-00006 · DOI
- Teitelbaum, 1998, Minocycline-related autoimmune hepatitis: case series and literature review, Arch Pediatr Adolesc Med, 152, 1132, 10.1001/archpedi.152.11.1132 · DOI
- Angulo, 1998, Coexistent minocycline-induced systemic lupus erythematosus and autoimmune hepatitis, Semin Arthritis Rheum, 28, 187, 10.1016/S0049-0172(98)80035-8 · DOI
- Herzog, 1997, Study of immune reactivity of minocycline-induced chronic active hepatitis, Dig Dis Sci, 42, 1100, 10.1023/A:1018817926394 · DOI
- Scully, 1993, Diclofenac-induced hepatitis: 3 cases with features of autoimmune chronic active hepatitis, Dig Dis Sci, 38, 744, 10.1007/BF01316809 · DOI
- Benninger, 1999, Acute hepatitis induced by greater celandine (chelidonium majus), Gastroenterology, 117, 1234, 10.1016/S0016-5085(99)70410-5 · DOI
- Berardinis, 2000, Human microsomal epoxide hydrolase is the target of germander-induced autoantibodies on the surface of human hepatocytes, Mol Pharm, 58, 542, 10.1124/mol.58.3.542 · DOI
- Hong, 1997, Is melatonin associated with the development of autoimmune hepatitis?, J Clin Gastroenterol, 25, 376, 10.1097/00004836-199707000-00020 · DOI
- Kamiyama, 1997, Autoimmune hepatitis triggered by administration of an herbal medicine, Am J Gastroenterol, 92, 703
- Al-Kawas, 1981, Allopurinol hepatotoxicity: report of two cases and review of literature, Ann Intern Med, 95, 588, 10.7326/0003-4819-95-5-588 · DOI
- Maddrey, 1975, Severe hepatitis from methyldopa, Gastroenterology, 68, 351, 10.1016/S0016-5085(75)80018-7 · DOI
- Saggie, 1979, Patterns of hepatic injury by methyldopa, S Afr Med J, 55, 25
- Stricker, 1988, Hepatic injury associated with the use of nitrofurans: a clinicopathological study of 52 reported cases, Hepatology, 8, 599, 10.1002/hep.1840080327 · DOI
- Marotta, 1998, Pemoline hepatotoxicity in children, J Pediatr, 132, 894, 10.1016/S0022-3476(98)70329-4 · DOI
- Moradpour, 1994, Chlorpromazine-induced vanishing bile duct syndrome leading to biliary cirrhosis, Hepatology, 20, 1437, 10.1002/hep.1840200610 · DOI
- Derby, 1993, Erythromycin-associated cholestatic hepatitis, Med J Aust, 158, 600, 10.5694/j.1326-5377.1993.tb137625.x · DOI
- O'Donohue, 2000, Co-amoxiclav jaundice: clinical and histological features and HLA Class II association, Gut, 47, 717, 10.1136/gut.47.5.717 · DOI
- Tarazi, 1993, Sulindac-associated hepatic injury: analysis of 91 cases reported to the Food and Drug Administration, Gastroenterology, 104, 569, 10.1016/0016-5085(93)90428-F · DOI
- Nissan, 1996, Captopril-associated pseudochangitis, Arch Surg, 131, 670, 10.1001/archsurg.1996.01430180096021 · DOI
- Tholakanahalli, 1998, Glibenclamide-induced cholestasis, West J Med, 168, 274
- Larrey, 1989, Genetic predisposition to drug hepatotoxicity: role in hepatitis caused by amineptine, a tricyclic antidepressant, Hepatology, 10, 168, 10.1002/hep.1840100208 · DOI
- Dujovne, 1967, Sulfonamide hepatic injury, N Engl J Med, 277, 785, 10.1056/NEJM196710122771503 · DOI
- Aaron, 1985, Diphenylhydantoin-induced hepatotoxicity, Am J Gastroenterol, 80, 200
- Larrey, 1997, Genetic predisposition to drug-induced hepatotoxicity, J Hepatol, 26, 12, 10.1016/S0168-8278(97)80492-8 · DOI
- Daly, 1995, Molecular basis of polymorphic drug metabolism, J Mol Med, 73, 539, 10.1007/BF00195139 · DOI
- Shear, 1988, Anticonvulsant hypersensitivity syndrome: in vitro assessment of risk, J Clin Invest, 82, 1826, 10.1172/JCI113798 · DOI
- Rieder, 1989, Diagnosis of sulfonamide hypersensitivity reactions by in vitro “rechallenge” with hydroxylamine metabolites, Ann Intern Med, 110, 286, 10.7326/0003-4819-110-4-286 · DOI
- Hoft, 1981, Halothane hepatitis in three pairs of closely related women, N Engl J Med, 304, 1023, 10.1056/NEJM198104233041707 · DOI
- Otsuka, 1985, HLA antigens in patients with unexplained hepatitis following halothane anesthesia, Acta Anaesthesiol, 29, 497, 10.1111/j.1399-6576.1985.tb02242.x · DOI
- Berson, 1994, Possible role of HLA in hepatotoxicity: an exploratory study in 71 patients with drug-induced idiosyncratic hepatitis, J Hepatol, 20, 336, 10.1016/S0168-8278(94)80004-9 · DOI
- Maria, 1997, Diagnostic value of specific T cell reactivity to drugs in 95 cases of drug induced liver injury, Gut, 41, 534, 10.1136/gut.41.4.534 · DOI
Cited by
Sorted by citations
Andrade, R. J., Chalasani, N., Björnsson, E. S., Suzuki, A., Kullak-Ublick, G. A., Watkins, P. B., Devarbhavi, H., Merz, M., Lucena, M. I., Kaplowitz, N., et al. (2019) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0105-0 · Cited by 924
Self-citationAndrade, R. J., Aithal, G. P., de Boer, Y. S., Liberal, R., Gerbes, A., Regev, A., Terziroli Beretta-Piccoli, B., Schramm, C., Kleiner, D. E., De Martin, E., et al. (2023) · Journal of Hepatology · doi:10.1016/j.jhep.2023.04.033 · Cited by 166
Chakraborty, M., Fullerton, A. M., Semple, K., Chea, L. S., Proctor, W. R., Bourdi, M., Kleiner, D. E., Zeng, X., Ryan, P. M., Dagur, P. K., et al. (2015) · Hepatology · doi:10.1002/hep.27764 · Cited by 64
Significance of antibodies to soluble liver antigen/liver pancreas: a large French study
Eyraud, V., Chazouilleres, O., Ballot, E., Corpechot, C., Poupon, R., & Johanet, C. (2009) · Liver International · doi:10.1111/j.1478-3231.2009.01986.x · Cited by 58
Metadata
- Authors
- Liu, Z.-X., & Kaplowitz, N.
- Venue
- Clinics in Liver Disease
- Publisher
- Elsevier BV
- Published
- 2002-08
- Volume
- 6
- Issue
- 3
- Pages
- 755-774
- ISSN
- 1089-3261
- Cited by
- 170
- References
- 3
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review