- 现金
- 62111 元
- 精华
- 26
- 帖子
- 30437
- 注册时间
- 2009-10-5
- 最后登录
- 2022-12-28
|
Multiple HBV Quasispecies and Immune-Escape Mutations Are Present in HBV Surface Antigen and Reverse Transcriptase of Patients with Acute Hepatitis B
Marianna Aragri1,*, Claudia Alteri1,*, Arianna Battisti1, Domenico Di Carlo1, Carmine Minichini2, Caterina Sagnelli3, Maria Concetta Bellocchi1, Maria Antonietta Pisaturo2, Mario Starace2, Daniele Armenia1, Luca Carioti1, Michela Pollicita1, Romina Salpini1, Evangelista Sagnelli2, Carlo Federico Perno1, Nicola Coppola2,§ and Valentina Svicher1,§
-
Author Affiliations
1Department of Experimental Medicine and Surgery, University of Rome “Tor Vergata”, Italy
2Department of Mental Health and Public Medicine, Section of Infectious Diseases, Second University of Naples, ITALY
3Department of Clinical and Experimental Medicine and Surgery, Second University of Naples, Naples, Italy
Correspondence: Carlo Federico Perno, Valentina Svicher, University of Rome Tor Vergata, Department of Experimental Medicine and Surgery, Via Montpellier 1, 00133 Rome, e-mail: [email protected]; [email protected], phone: 0039 06 72596566, 0039 06 72596564
↵* Marianna Aragri and Claudia Alteri equally contributed to this study
↵§ Joint last authorship
Abstract
Background. To characterize HBV RT and HBsAg quasispecies heterogeneity in acute HBV-infected (AHB) patients and to define their clinical value.
Methods. 62 patients with AHB (44 genotype-D and 18 genotype-A) were enrolled from 2000 to 2010. Plasma-samples obtained at first observation were analyzed by Ultra-deep-pyrosequencing (UDPS). Extent of HBsAg amino acid variability was measured by Shannon-Entropy.
Results. Median (IQR) ALT and serum HBV-DNA were 2,544(1,938-3,078)U/L and 5.88(4.47-7.37)log10IU/ml, respectively. Although most patients serologically resolved AHB, only 54.1% developed anti-HBs.
A viral-population with >1 immune-escape mutation was found in 53.2% of patients (intra-patient prevalence range:0.16%-100%). Notably, by Shannon-Entropy, an higher genetic-variability at HBsAg amino acid positions 130, 133, and 157 significantly correlated with no anti-HBs production in genotype-D (P<0.05).
Stop-codons were detected in 19.3% of patients (intra-patient prevalence range:1.6%-47.5%). They occurred at 11 HBsAg-positions including 172 and 182, known to increase HBV oncogenic-potential.
Finally, >1 drug-resistance mutation was detected in 8.1% of patients (intra-patient prevalence range: 0.11%-47.5% for primary-mutations, and 10.5%-99.9% for compensatory ones).
Conclusions. AHB is characterized by complex array of viral quasispecies with reduced antigenicity/immunogenicity, and enhanced oncogenic-potential. These viral variants may induce difficult-to-treat HBV forms, favor HBV-reactivation upon iatrogenic-immunosuppression even years after infection, and potentially affect current HBV-vaccination efficacy.
© The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail [email protected].
|
|