Effect of Direct Antiviral Therapy Against HCV on CD4+ T Cell Count in Patients with HIV-HCV Coinfection.

IF 1.5 Q4 INFECTIOUS DISEASES
Biagio Pinchera, Emanuela Zappulo, Antonio Riccardo Buonomo, Maria Rosaria Cotugno, Giovanni Di Filippo, Francesco Borrelli, Simona Mercinelli, Riccardo Villari, Ivan Gentile
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Abstract

Background: HCV-related liver disease is an important cause of morbidity and mortality in patients with HIV infection. It is well known that the response rates to HCV therapy are similar between HCV-monoinfected patients and HIV-HV coinfected ones. The aim of this study was to evaluate the impact of HCV eradication on CD4 + T cell count in a population of HIV-HCV coinfected patients.

Materials and methods: We enrolled patients with HIV-HCV coinfection attending the Infectious Diseases Unit of the A.O.U. Federico II of Naples, from January 2016 to February 2019, treated with ART (AntiRetroviral Therapy) and DAAs (Direct Antiviral Agents). For each patient, we evaluated HIV and HCV viral load and CD4+ T cell count before starting therapy with DAAs, by SVR12 time and by SVR48 time. Fibrosis was evaluated by the mean of Fibroscan®.

Results: Fifty-two patients were enrolled, 40 males. Fibrosis score was F0-F3 in 15 patients and cirrhosis in the remaining 11 (all in Child-Pugh class A). All had been receiving ART, and all were treated with DAAs. Only patient who had not achieved HIV viral suppression for non-compliance also experienced a relapse of HCV infection after the end of DAAs. In all patients, we observed that the CD4+ T cell count at baseline did not show significant variations compared to SVR12 and SVR48 time. We also assessed CD4 count in relation to HIV categories and stage of liver disease, see Table 1. Also, based on the assessments of the subclasses considered, there were no significant changes in the CD4 + T cell count.

Conclusion: Our study shows that HCV viral eradication obtained with DAAs in patients with HIV-HCV coinfection is not associated with significant changes in the CD4 + T cell count, regardless of CDC category and stage of liver disease.

直接抗病毒治疗对HIV-HCV合并感染患者CD4+ T细胞计数的影响
背景:hcv相关性肝病是HIV感染患者发病和死亡的重要原因。众所周知,HCV单感染患者和HIV-HV合并感染患者对HCV治疗的应答率相似。本研究的目的是评估HCV根除对HIV-HCV合并感染患者群体中CD4 + T细胞计数的影响。材料和方法:我们招募了2016年1月至2019年2月在那不勒斯A.O.U. Federico II传染病科接受ART(抗逆转录病毒治疗)和DAAs(直接抗病毒药物)治疗的HIV-HCV合并感染患者。对于每位患者,我们在开始DAAs治疗前按SVR12时间和SVR48时间评估HIV和HCV病毒载量和CD4+ T细胞计数。通过Fibroscan®的平均值评估纤维化。结果:入组患者52例,男性40例。15例患者纤维化评分为F0-F3,其余11例患者肝硬化(均为Child-Pugh A级)。所有患者均接受ART治疗,并均接受daa治疗。只有未达到HIV病毒抑制的患者在daa结束后也经历了HCV感染复发。在所有患者中,我们观察到基线时的CD4+ T细胞计数与SVR12和SVR48时间相比没有显着变化。我们还评估了CD4计数与HIV类型和肝脏疾病阶段的关系,见表1。此外,根据所考虑的亚类评估,CD4 + T细胞计数没有显着变化。结论:我们的研究表明,在HIV-HCV合并感染的患者中,DAAs获得的HCV病毒根除与CD4 + T细胞计数的显著变化无关,与疾病的CDC类别和阶段无关。
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来源期刊
CiteScore
3.00
自引率
6.70%
发文量
61
审稿时长
16 weeks
期刊介绍: About Dove Medical Press Dove Medical Press Ltd is part of Taylor & Francis Group, the Academic Publishing Division of Informa PLC. We specialize in the publication of Open Access peer-reviewed journals across the broad spectrum of science, technology and especially medicine. Dove Medical Press was founded in 2003 with the objective of combining the highest editorial standards with the ''best of breed'' new publishing technologies. We have offices in Manchester and London in the United Kingdom, representatives in Princeton, New Jersey in the United States, and our editorial offices are in Auckland, New Zealand. Dr Scott Fraser is our Medical Director based in the UK. He has been in full time clinical practice for over 20 years as well as having an active research interest.
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