Homberg J C, Abuaf N, Helmy-Khalil S, Biour M, Poupon R, Islam S, Darnis F, Levy V G, Opolon P, Beaugrand M
Hepatology. 1985 Sep-Oct;5(5):722-7. doi: 10.1002/hep.1840050504.
A study from five hepatology units documenting 157 cases of drug-induced hepatitis and a second study from a laboratory of immunology which tested more than 100,000 sera permitted us to establish the frequency of antiorganelle antibodies and their diagnostic value in drug-induced hepatitis. In drug-induced hepatitis caused by a heterogenous group of drugs consisting of ajmaline, aminopterine, isaxonine, isoniazid, perhexiline, phenylbutazone and troleandromycine, antiorganelle antibodies were absent or rare. In drug-induced hepatitis caused by another heterogenous group of drugs, including clometacin, fenofibrate, oxyphenisatin and papaverine, antismooth muscle, antinucleus and antimitochondria antibodies were found in isolation or in different combinations in 70% of cases. From the presence of antismooth muscle antibodies in sera, we could trace 30 cases of clometacin-induced hepatitis. The third group included drug-induced hepatitis with special antibody:iproniazid-induced hepatitis with antimitochondrial antibody 6 and tienilic acid (ticrynafen)-induced hepatitis with antiliver/kidney microsome antibody 2 (anti-LKM2). These two antibodies are rare in routine sera and were absent in patients who received the drug and had no liver damage. From the presence of corresponding antibodies, we detected six cases of iproniazid-induced hepatitis and 67 cases of tienilic acid-induced hepatitis. Antiorganelle antibodies found in high titers disappeared in 2 to 24 months following withdrawal of the offending drug. The fourth group was represented by halothane-induced hepatitis; antiliver/kidney microsome antibody 1 was weak and infrequent. Similarities between drug-induced hepatitis of the second group and lupoïd hepatitis suggest that drugs may reveal this spontaneous disorder.(ABSTRACT TRUNCATED AT 250 WORDS)
来自五个肝病科记录了157例药物性肝炎病例的一项研究,以及来自一个免疫学实验室检测了超过10万份血清的另一项研究,使我们能够确定抗细胞器抗体在药物性肝炎中的出现频率及其诊断价值。在由一组异质性药物(包括阿义马林、氨蝶呤、异沙生宁、异烟肼、哌克昔林、保泰松和醋竹桃霉素)引起的药物性肝炎中,抗细胞器抗体不存在或罕见。在由另一组异质性药物(包括氯美辛、非诺贝特、奥昔芬净和罂粟碱)引起的药物性肝炎中,抗平滑肌、抗核和抗线粒体抗体在70%的病例中单独或不同组合出现。从血清中存在抗平滑肌抗体,我们追踪到30例氯美辛引起的肝炎病例。第三组包括具有特殊抗体的药物性肝炎:异烟肼引起的肝炎伴有抗线粒体抗体6,替尼酸(替克瑞纳芬)引起的肝炎伴有抗肝/肾微粒体抗体2(抗LKM2)。这两种抗体在常规血清中罕见,在服用该药物但无肝损伤的患者中不存在。从相应抗体的存在情况,我们检测到6例异烟肼引起的肝炎和67例替尼酸引起的肝炎。停药后2至24个月,高滴度的抗细胞器抗体消失。第四组以氟烷引起的肝炎为代表;抗肝/肾微粒体抗体1较弱且不常见。第二组药物性肝炎与狼疮样肝炎之间的相似性表明,药物可能会揭示这种自发性疾病。(摘要截断于250字)