Clinic of Infectious Diseases, Vita-Salute University, San Raffaele Scientific Institute, Milan, Italy; Experimental Medicine and Surgery "F. Magrassi e A. Lanzara", Second University of Naples, Naples, Italy.
Clinic of Infectious Diseases, Vita-Salute University, San Raffaele Scientific Institute, Milan, Italy.
Braz J Infect Dis. 2014 Mar-Apr;18(2):164-9. doi: 10.1016/j.bjid.2013.06.005. Epub 2013 Oct 25.
To evaluate changes in liver histology in patients with human immunodeficiency virus/hepatitis C virus coinfection non-responders to a suboptimal Interferon+Ribavirine regimen.
We investigated 49 patients with two sequential liver biopsies: 18 were non-responders to Interferon+Ribavirine treatment (Group hepatitis C virus Rx) administered after the 1st liver biopsy who underwent a 2nd liver biopsy after a median period of 3.92 year and 31 were patients who remained untreated for hepatitis C virus disease (Group hepatitis C virus untreated) after the 1st liver biopsy because of refusal and underwent a 2nd liver biopsy after a median period of 5.05-years. Most patients in both groups were under highly active antiretroviral therapy. At the time of 1st liver biopsy similar degrees of necro-inflammation, fibrosis and steatosis were observed in both groups. Changes in liver lesions between 1st and 2nd liver biopsys were adjusted for different intervals between liver biopsys by a mathematic formula.
Liver fibrosis did not change in 88.9% of patients in Group hepatitis C virus Rx and in 77.4% in Group hepatitis C virus untreated. A marked deterioration in liver fibrosis was observed in 5 (16%) patients in Group hepatitis C virus untreated and in none in Group hepatitis C virus treated. Necro-inflammation and steatosis remained substantially unchanged in both groups.
Liver histology remained substantially unchanged in human immunodeficiency virus/hepatitis C virus patients non-responder to anti-hepatitis C virus therapy over 4 years observation, suggesting an effective anti-hepatitis C virus early treatment for all hepatitis C virus/human immunodeficiency virus coinfected patients who can reasonably tolerate therapy.
评估人类免疫缺陷病毒/丙型肝炎病毒合并感染对不理想的干扰素+利巴韦林方案无反应患者的肝组织学变化。
我们研究了 49 例连续两次肝活检的患者:18 例对干扰素+利巴韦林治疗无反应(组丙型肝炎病毒 Rx),在第一次肝活检后接受治疗,中位时间为 3.92 年后进行第二次肝活检,31 例丙型肝炎病毒患者未接受治疗在第一次肝活检后因拒绝而未接受治疗(组丙型肝炎病毒未治疗),并在中位时间为 5.05 年后进行第二次肝活检。两组大多数患者均接受高效抗逆转录病毒治疗。在第一次肝活检时,两组的坏死性炎症、纤维化和脂肪变性程度相似。通过数学公式调整两组之间不同肝活检间隔的肝病变变化。
丙型肝炎病毒 Rx 组 88.9%的患者肝纤维化无变化,丙型肝炎病毒未治疗组 77.4%的患者肝纤维化无变化。丙型肝炎病毒未治疗组 5 例(16%)患者肝纤维化明显恶化,而丙型肝炎病毒治疗组无恶化。两组的坏死性炎症和脂肪变性基本保持不变。
在 4 年多的观察期内,对丙型肝炎病毒治疗无反应的人类免疫缺陷病毒/丙型肝炎病毒患者的肝组织学基本保持不变,这表明对所有丙型肝炎病毒/人类免疫缺陷病毒合并感染患者进行有效的早期抗丙型肝炎病毒治疗是合理的,这些患者可以合理地耐受治疗。