Literature DB >> 2190593

Immunotoxic side-effects of drug therapy.

J A Mitchell1, E M Gillam, L A Stanley, E Sim.   

Abstract

Adverse reactions to drugs in which an immune mechanism is responsible for toxicity have been described as idiosyncratic. Understanding these toxic effects is important to enable the identification of patients at risk. The specific toxic side effects considered are heparin-induced thrombocytopenia, penicillin-induced haemolytic anaemia, hepatitis as a result of halothane and tienilic acid therapy, quinine- and quinidine-dependent thrombocytopenia, methyldopa-induced haemolytic anaemia and immune-complex disease following administration of hydralazine, procainamide and penicillamine. The molecular mechanisms of immunotoxicity are presented where such information is available although more than one effect may contribute to the observed pattern of toxicity. The initial events leading to antibody production in certain individuals in response to drug therapy are not understood and, in many of the examples described, antibody production occurs in some patients who do not subsequently experience clinical problems. Clinically serious adverse effects involving immune reactions are infrequent, and a range of genetic and environmental circumstances need to be present simultaneously in an individual before toxicity develops. The ability to metabolise a particular drug has been shown to be one major predisposing factor in toxicity; the immunocompetence of the patient is likely to be another. Both of these considerations are subject to genetic and environmental controls, including infection and disease.

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Year:  1990        PMID: 2190593     DOI: 10.2165/00002018-199005030-00002

Source DB:  PubMed          Journal:  Drug Saf        ISSN: 0114-5916            Impact factor:   5.606


  98 in total

1.  The chemical induction of systemic lupus erythematosus and lupus-like illnesses.

Authors:  M M Reidenberg
Journal:  Arthritis Rheum       Date:  1981-08

2.  Immune regulatory abnormalities produced by procainamide.

Authors:  K B Miller; D Salem
Journal:  Am J Med       Date:  1982-10       Impact factor: 4.965

3.  Depression of hepatic cytochrome P-450-dependent mixed function oxidases during infection with encephalomyocarditis virus.

Authors:  K W Renton
Journal:  Biochem Pharmacol       Date:  1981-08-15       Impact factor: 5.858

Review 4.  Drug-induced platelet destruction.

Authors:  T Hackett; J G Kelton; P Powers
Journal:  Semin Thromb Hemost       Date:  1982-04       Impact factor: 4.180

5.  The nature of the alpha-methyldopa red-cell antibody.

Authors:  A F LoBuglio; J H Jandl
Journal:  N Engl J Med       Date:  1967-03-23       Impact factor: 91.245

6.  Hydralazine binds covalently to complement component C4. Different reactivity of C4A and C4B gene products.

Authors:  E Sim; S K Law
Journal:  FEBS Lett       Date:  1985-05-20       Impact factor: 4.124

7.  Effects of long-term procainamide therapy on immunoglobulin synthesis.

Authors:  C L Yu; M Ziff
Journal:  Arthritis Rheum       Date:  1985-03

8.  Hydralazine and procainamide inhibit T cell DNA methylation and induce autoreactivity.

Authors:  E Cornacchia; J Golbus; J Maybaum; J Strahler; S Hanash; B Richardson
Journal:  J Immunol       Date:  1988-04-01       Impact factor: 5.422

9.  Association of antibody to histone complex H2A-H2B with symptomatic procainamide-induced lupus.

Authors:  M C Totoritis; E M Tan; E M McNally; R L Rubin
Journal:  N Engl J Med       Date:  1988-06-02       Impact factor: 91.245

10.  Autoantibody formation in D-penicillamine-treated rheumatoid arthritis.

Authors:  J P Camus; J C Homberg; J Crouzet; C Mery; F Delrieu; P Massias; N Abuaf
Journal:  J Rheumatol Suppl       Date:  1981 Jan-Feb
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  3 in total

Review 1.  Drug Adverse Reaction Target Database (DART) : proteins related to adverse drug reactions.

Authors:  Zhi Liang Ji; Lian Yi Han; Chun Wei Yap; Li Zhi Sun; Xin Chen; Yu Zong Chen
Journal:  Drug Saf       Date:  2003       Impact factor: 5.606

Review 2.  Drug-related lupus. Incidence, mechanisms and clinical implications.

Authors:  L E Adams; E V Hess
Journal:  Drug Saf       Date:  1991 Nov-Dec       Impact factor: 5.606

3.  Low-sodium diet induces atherogenesis regardless of lowering blood pressure in hypertensive hyperlipidemic mice.

Authors:  Fernanda B Fusco; Diego J Gomes; Kely C S Bispo; Veronica P Toledo; Denise F Barbeiro; Vera L Capelozzi; Luzia N S Furukawa; Ana P P Velosa; Walcy R Teodoro; Joel C Heimann; Eder C R Quintao; Marisa Passarelli; Edna R Nakandakare; Sergio Catanozi
Journal:  PLoS One       Date:  2017-05-08       Impact factor: 3.240

  3 in total

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