Hepatitis C virus infection associated with liver-kidney microsomal antibody type 1 (LKM1) autoantibodies in children

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• 作者：Flavia Bortolotti ; Luigi Muratori ; Paloma Jara ; Loreto Hierro ; Gabriella Verucchi ; Raffaella Giacchino ; Cristiana Barbera ; Lucia Zancan ; Maria Guido ; Massimo Resti ; Sabrina Pedditzi ; Francesco Bianchi ; Angelo Gatta
• 刊名：The Journal of Pediatrics
• 出版年：2003
• 出版时间：February 2003
• 年：2003
• 卷：142
• 期：2
• 页码：185-190
• 全文大小：120 K

文摘

Objective To evaluate the clinical pattern and evolution of chronic hepatitis C in children with liver/kidney microsomal antibody type 1 autoantibodies (LKM1). Study design A multicenter, retrospective study, including the following groups of children with hepatitis C virus infection: (1) 21 consecutive LKM1-positive patients, (2) 42 age- and sex- matched LKM1-negative patients, and (3) 4 interferon-induced LKM1-positive cases. LKM1 reactivity to human microsomes and recombinant cytochrome P450IID6 (CYP2D6) was assayed by immunoblotting. Results Clinical and biochemical features overlapped in LKM1-positive and LKM1-negative children, but a fibrosis score >3 (range 0-6) was significantly more frequent (P = .04) in the former. Reactivity to microsomal protein and CYP2D6 was significantly (P = .02) associated with LKM1 titers ≥1:320 and was found in 39 % of patients, including severe cases and both children (of 4 treated) who achieved a sustained alanine aminotransferase (ALT) normalization after steroid treatment. Five of 7 LKM1-positive children treated with interferon had an ALT exacerbation. Conclusions LKM1-positive hepatitis C in children is characterized by a wide spectrum of biochemical, serologic, and histologic features. Whether autoimmunity may contribute to liver damage in a subgroup of patients with more severe liver disease, high LKM1 titers, and reactivity to CYP2D6 is a question deserving further investigation. (J Pediatr 2003;142:185-90)