How to Adjust the Action Steps for Achieving the Global Hepatitis Virus (HBV/HCV/HDV) Elimination Targets?

A special issue of Viruses (ISSN 1999-4915). This special issue belongs to the section "Viral Immunology, Vaccines, and Antivirals".

Deadline for manuscript submissions: closed (30 November 2024) | Viewed by 11499

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Institute of Biostructure and Bioimaging, National Research Council, Via De Amicis 95, 80145 Naples, Italy
Interests: hepatitis viruses; HBV; HCV; HDV; hepatitis B HBeAg negative virus
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Special Issue Information

Dear Colleagues,

Objective: "Adjusted action steps for achieving global hepatitis virus (HBV/HCV/HDV) elimination".

Introduction: The WHO’s goal of hepatitis elimination by 2030 will not be fulfilled because chronic viral liver disease remains a highly significant global health concern. Current anti-HCV antivirals can cure more than 95% of HCV infections but do not provide protection from re-infection, and without HCV vaccines, the elimination of HCV infection is impossible. Life-long suppression of hepatitis B virus (HBV) replication with nucleot(s)ide analogues is far from ideal because it is burdened by cost and adherence problems. Many new drugs aiming to increase the rate of functional HBV cures (serum HBsAg and HDV-DNA clearance) are under clinical investigation, but none are commercially available. Furthermore, there is an unmet need to fully exploit the potential of old and new drugs with more personalized treatment approaches on accurate virologic, immunologic, and clinic–pathologic profiling. The clinical efficacy of the new anti-HDV drug to inhibit viral entry into the hepatocyte remains to be fully elucidated. This Special Issue will gather manuscripts from renowned experts in different fields of viral hepatitis, aiming to propose new action steps towards eliminating the global clinical burden of viral hepatitis caused by HBV, HCV and HDV.

Summary: The global hepatitis strategy of the World Health Organization (WHO), endorsed by all WHO Member States, aimed to reduce new infections with hepatitis B, C and D (HBV, HCV and HDV) by 90% and deaths by 65% between 2016 and 2030. At the beginning of 2020, there were an estimated 56.8 million viraemic HCV infections globally; although this number represents a consistent decrease from 2016, the forecasts suggest that we are not currently on track to achieve global elimination targets by 2030. In 2020, because of continued increases in HCV infections in the USA, the Center for Disease Control (CDC) released universal screening recommendations for adults including pregnant women [2]; since the proper identification of perinatally infected children and their referral to curative treatment are critical to eliminating hepatitis C, the CDC recently released new screening recommendations [3]. Direct-acting antiviral medicines (DAAs) can cure more than 95% of persons with HCV infection, but they do not provide protection from re-infection, and access to diagnosis and treatment is low. There are currently no effective vaccines against hepatitis C, without which we cannot eliminate HCV infection. Similarly in spite of a reduction worldwide HBV/HDV infections remain a significant global burden of liver disease [4-5]. Current HBV treatment relies on the life-long suppression of viral replication with nucleot(s)ide analogues (NUC) and NUC discontinuation before HBsAg loss is questionable. Virological and clinical reasons argue against NUC discontinuation in the vast majority of patients with chronic hepatitis B, and there is an unmet need for new biomarkers to profile and stratify NUC treated patients: (a) to identify those with high probability of HBsAg loss after NUC discontinuation; (b) those who could benefit from a short, combined treatment with new drugs to anticipate the time of NUC treatment discontinuation; (d) those who have to be maintained in a continuous pharmacological viral suppression. Extensive research is in progress with the goal of achieving a functional cure for HBV infection (negative serum HBsAg), and clinical trials with many mew drugs with either virologic or immunologic targets are ongoing; currently, however, there are no new drugs commercially available. The overall prevalence of HDV infection is underestimated because of the lack of universal screening for HDV infection in HBsAg-positive carriers [5]. A new anti-HDV drug (Myrcludex) has become available; however, its clinical efficacy remains to be fully demonstrated [6]. Finally, there is an urgent ethical need to define the value of new medicinal products in terms of cost-opportunity, from the point of view of the patient and national health systems, in order to ensure referral to care and curative treatments for as many patients as possible worldwide. Bearing in mind Michelangelo’s aphorism, “The greatest danger for most of us is not that our aim is too high and we miss it, but that it is too low and we reach it“, and prompted by the wise lesson from Confucius, who said “when it is obvious that the goal cannot be reached, don't adjust the goal, adjust the action steps”, we wish to organize and publish a Special Issue of Viruses devoted to manuscripts written by renowned experts in different virologic fields of viral hepatitis, aiming to propose new action steps towards eliminating the global clinical burden of viral hepatitis caused by HBV, HCV and HDV.

  1. Polaris Observatory HCV Collaborators. Global change in hepatitis C virus prevalence and cascade of care between 2015 and 2020: a modelling study. Lancet Gastroenterol Hepatol. 2022 May;7(5):396-415. doi:10.1016/S2468-1253(21)00472-6.
  2. Schillie S et al. CDC Recommendations for Hepatitis C Screening Among Adults United States, 2020. MMWR Recomm Rep 2020;69 (No. RR-29):1–17].
  3. Panagiotakopoulos L et Al. CDC Recommendations for Hepatitis C Testing Among Perinatally Exposed Infants and Children United States, 2023. MMWR Recomm Rep 2023;72(No. RR-4):1–19]. doi: http://dx.doi.org/10.15585/mmwr.rr7204a1.
  4. Cortesi PA et Al. Hepatitis B and C in Europe: an update from the Global Burden of Disease Study 2019; Lancet Public Health 2023 Sept;8(9): e701-e716 doi:10.1016/S2468-2667(23)00149-4.
  5. Colombatto P et Al. Management and Treatment of Patients with Chronic Hepatitis B: Towards Personalized Medicine. Viruses. 2022 Mar 28;14(4):701. doi:10.3390/v14040701.
  6. Brunetto MR et Al. EASL Clinical Practice Guidelines on Hepatitis Delta Virus J. Hep. 2023(Aug);79(2):433-460 doi:10.1016/j.jhep.2023.05.001.

Prof. Dr. Ferruccio Bonino
Guest Editor

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Keywords

  • antivirals
  • chronic viral hepatitis infections
  • HBV
  • HBV functional cure
  • HCV
  • HCV vaccine
  • HDV
  • HDV-RNA
  • anti-HD

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Related Special Issue

Published Papers (8 papers)

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Research

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12 pages, 1433 KiB  
Article
Efficacy of Different Combinations of Direct-Acting Antivirals Against Different Hepatitis C Virus-Infected Population Groups: An Experience in Tertiary Care Hospitals in West Bengal, India
by Sagnik Bakshi, Partha Chattopadhyay, Mahiuddin Ahammed, Raina Das, Moumita Majumdar, Supradip Dutta, Shreyasi Nath, Anwesha Ghosh, Uttaran Bhattacharjee, Upasana Baskey and Provash Chandra Sadhukhan
Viruses 2025, 17(2), 269; https://doi.org/10.3390/v17020269 - 16 Feb 2025
Viewed by 593
Abstract
Hepatitis C virus (HCV) is a global public health problem, but advancements in HCV treatment have improved the cure rate. This study evaluated the effectiveness of direct-acting antivirals (DAAs) in HCV-infected patients from May 2021 to April 2023 in collaboration with tertiary care [...] Read more.
Hepatitis C virus (HCV) is a global public health problem, but advancements in HCV treatment have improved the cure rate. This study evaluated the effectiveness of direct-acting antivirals (DAAs) in HCV-infected patients from May 2021 to April 2023 in collaboration with tertiary care hospitals in West Bengal. The HCV viral load was monitored via qRT-PCR. Sanger sequencing was performed to determine the HCV genotypes. The clinicians prescribed the patient treatment regime. The maximum number of patients in the study population (N = 398) were compensated cirrhosis patients (46.28%). The overall SVR rate of the study population was 94.47%. The decompensated cirrhosis patients experienced the lowest SVR rate (88.89%). The maximum number of patients were prescribed sofosbuvir/daclatasvir (63.77%), and the lowest SVR rate (93.23%) was observed with this treatment regime. In the study population, GT-3 was the predominant (67.43%) circulating genotype, followed by GT-1 and -4. Among 398 patients, 22 (5.53%) were non-responsive to DAA treatment. Out of these 22 non-responder patients, 77.27% (n = 17) were GT-3-infected (3a:10; 3b:07), followed by GT-1 (1c: 04; 1b: 01). Thus, increasing numbers of DAA non-responsive cases among HCV GT-3-infected and decompensated cirrhosis patients may pose serious threats in the future. Full article
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12 pages, 2040 KiB  
Article
Serological and Molecular Characterization of the Hepatitis B Virus in Blood Donors in Maputo City, Mozambique
by Olga Maquessene, Osvaldo Laurindo, Lúcia Chambal, Nalia Ismael and Nédio Mabunda
Viruses 2025, 17(1), 94; https://doi.org/10.3390/v17010094 - 13 Jan 2025
Viewed by 1235
Abstract
Hepatitis B virus (HBV) is a major public health concern responsible for hepatitis and hepatocellular carcinoma (HCC) worldwide. In Mozambique, HBsAg prevalence is high and endemic, and despite the strategies to mitigate the spread of the disease, the HCC incidence is still high [...] Read more.
Hepatitis B virus (HBV) is a major public health concern responsible for hepatitis and hepatocellular carcinoma (HCC) worldwide. In Mozambique, HBsAg prevalence is high and endemic, and despite the strategies to mitigate the spread of the disease, the HCC incidence is still high and one of the highest in the world. There is still limited data on the serological profile and molecular epidemiology of HBV in Mozambique given the burden of this disease. In this study, we aimed to describe the serological and molecular characterization of HBV among blood donors. We conducted a cross-sectional survey from November 2014 to October 2015 at the Blood Bank of the Hospital Central de Maputo. Serological testing and molecular testing were performed. The frequency of HBV infection was estimated at 4.4% and was higher among males (79.1%), individuals aged 25–39 years (55.2%), and replacement donors (89.6%). The median viral load of HBV-positive blood donors was 1288.5 IU/mL, and 43.8% had a viral load higher than 2000 IU/mL. Most of the sequenced samples (94.3%) belonged to subgenotype A1. These findings underscore the importance of ongoing surveillance to inform effective HBV control strategies and present evidence about the burden of HBV among blood donors, which definitely requires attention, and clinical blood banks in Mozambique and in similar settings. Full article
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11 pages, 703 KiB  
Article
Unveiling Prevalence, Risk Factors, and Outcomes of Hepatitis D Among Vulnerable Communities in Romania
by Liana Gheorghe, Speranta Iacob, Irma Eva Csiki, Mihaela Ghioca, Razvan Iacob, Ileana Constantinescu, Bogdan Chiper, Laura Huiban, Cristina Muzica, Irina Girleanu, Nicoleta Tiuca, Sorina Diaconu, Daniela Larisa Sandulescu, Ion Rogoveanu, Andra Iulia Suceveanu, Florentina Furtunescu, Corina Pop and Anca Trifan
Viruses 2025, 17(1), 52; https://doi.org/10.3390/v17010052 - 31 Dec 2024
Viewed by 979
Abstract
Background: Hepatitis B (HBV) and Delta (HDV) virus infections pose critical public health challenges, particularly in Romania, where HDV co-infection is underdiagnosed. Methods: This study investigates the epidemiology, risk factors, and clinical outcomes of HBV/HDV co-infection in vulnerable populations, leveraging data from the [...] Read more.
Background: Hepatitis B (HBV) and Delta (HDV) virus infections pose critical public health challenges, particularly in Romania, where HDV co-infection is underdiagnosed. Methods: This study investigates the epidemiology, risk factors, and clinical outcomes of HBV/HDV co-infection in vulnerable populations, leveraging data from the LIVE(RO2) program. Conducted between July 2021 and November 2023, the program screened 320,000 individuals across 24 counties, targeting socially disadvantaged groups such as rural residents, the Roma community, and those lacking health insurance. Results: Among 6813 hepatitis B surface antigen (HBsAg)-positive individuals, HDV antibody prevalence was 4.87%, with active replication confirmed in 75.6% of HDV-positive cases. Regional disparities emerged, with higher HDV prevalence and replication rates in the Eastern region compared to the South. HDV-positive individuals were more likely to be younger, male, and from rural or socioeconomically disadvantaged backgrounds. Clinically, HDV co-infection correlated with increased liver stiffness, advanced fibrosis stages, and lower steatosis levels compared to HBV mono-infection. Psychiatric comorbidities were more prevalent among HDV-positive patients, highlighting the need for integrated care. Conclusions: This study underscores the urgent need for targeted public health interventions, including enhanced screening, education, and access to novel antiviral therapies like bulevirtide to address the significant burden of HBV/HDV co-infection in Romania. Full article
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9 pages, 1028 KiB  
Communication
Chronic Hepatitis B Genotype C Mouse Model with Persistent Covalently Closed Circular DNA
by Deok-Hwa Seo, Wonhee Hur, Juhee Won, Ji-Won Han, Seung-Kew Yoon, Songmee Bae, Kyun-Hwan Kim and Pil-Soo Sung
Viruses 2024, 16(12), 1890; https://doi.org/10.3390/v16121890 - 7 Dec 2024
Viewed by 1223
Abstract
Hepatitis B virus (HBV) can cause chronic infections, significantly increasing the risk of death from cirrhosis and hepatocellular carcinoma (HCC). A key player in chronic HBV infection is covalently closed circular DNA (cccDNA), a stable episomal form of viral DNA that acts as [...] Read more.
Hepatitis B virus (HBV) can cause chronic infections, significantly increasing the risk of death from cirrhosis and hepatocellular carcinoma (HCC). A key player in chronic HBV infection is covalently closed circular DNA (cccDNA), a stable episomal form of viral DNA that acts as a persistent reservoir in infected hepatocytes and drives continuous viral replication. Despite the development of several animal models, few adequately replicate cccDNA formation and maintenance, limiting our understanding of its dynamics and the evaluation of potential therapeutic interventions targeting cccDNA. In this study, we aimed to develop a mouse model to investigate cccDNA formation and maintenance. We infected C57BL/6 mice with recombinant adeno-associated virus (rAAV) carrying a 1.3-overlength HBV genome (genotype C) and collected liver tissue at various time points to assess cccDNA levels and viral replication. Our results demonstrated the successful establishment of a chronic hepatitis B mouse model using rAAV-HBV1.3, which supported persistent HBV infection with sustained cccDNA expression in hepatocytes. Serum levels of HBsAg and HBeAg were elevated for up to 12 weeks, while alanine transaminase (ALT) levels remained within the normal range, indicating limited liver damage during this period. We confirmed HBV DNA expression in hepatocytes, and importantly, cccDNA was detected using qPCR after Plasmid-Safe ATP-Dependent DNase treatment, which selectively removes non-cccDNA forms. Additionally, Southern blot analysis confirmed the presence of cccDNA isolated using the Hirt extraction method. This established model provides a valuable platform for studying the long-term maintenance of cccDNA in chronic HBV infection and offers an important tool for testing novel therapeutic strategies aimed at targeting cccDNA. Full article
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13 pages, 251 KiB  
Article
Hepatitis B Prevalence and Referral Rates in Vulnerable Populations Undergoing Community-Based Screening—Results from the LIVE(RO)2 Program
by Speranta Iacob, Irma Csiki, Razvan Iacob, Mihaela Ghioca, Ileana Constantinescu, Bogdan Chiper, Laura Huiban, Cristina Muzica, Irina Girleanu, Nicoleta Tiuca, Sorina Diaconu, Larisa Sandulescu, Ion Rogoveanu, Florentina Furtunescu, Corina Pop, Anca Trifan and Liana Gheorghe
Viruses 2024, 16(8), 1318; https://doi.org/10.3390/v16081318 - 18 Aug 2024
Cited by 1 | Viewed by 1827
Abstract
Background: Hepatitis B Virus (HBV) remains a major global health challenge, with significant morbidity and mortality associated with chronic infections. Methods: This study examines the epidemiology, screening, and risk factors associated with HBV in Romania, focusing on a comprehensive national screening program, LIVE(RO)2, [...] Read more.
Background: Hepatitis B Virus (HBV) remains a major global health challenge, with significant morbidity and mortality associated with chronic infections. Methods: This study examines the epidemiology, screening, and risk factors associated with HBV in Romania, focusing on a comprehensive national screening program, LIVE(RO)2, involving 320,000 individuals (majority of them considered vulnerable population). A questionnaire was used to collect information on the potential risk factors for HBV transmission. Results: The overall prevalence rate of HBV chronic infection among all the participants tested was 1.67% (confidence interval: 1.63–1.72%), with significant differences (p = 0.0001) between participants from the main geographical regions of residence (North-East 1.89%, South 1.38%, South-East 2.06%, and South-West 1.54%). Male persons aged 30–49 or 60–69 years old, from the rural and Eastern parts of Romania and non-Romanian ethnia, with a low level of education, unvaccinated, not married, unemployed, with family members with hepatitis, with personal histories of blood or blood product transfusion, surgical interventions, tattooing, hospitalizations, imprisonment, haemodialysis, unsafe sexual contacts, or with sexual transmitted infectious diseases were risk factors associated with HBsAg seropositivity. Conclusions: Our findings highlight significant demographic and epidemiological patterns of reduced HBV prevalence even in vulnerable persons, as well as modified risk factors and the impact of socio-economic factors. Full article

Review

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12 pages, 263 KiB  
Review
The Key Importance of Screening Underprivileged People in Order to Achieve Global Hepatitis Virus Elimination Targets
by Laura Gragnani, Monica Monti, Irene De Giorgi and Anna Linda Zignego
Viruses 2025, 17(2), 265; https://doi.org/10.3390/v17020265 - 14 Feb 2025
Cited by 1 | Viewed by 782
Abstract
Chronic hepatitis B (HBV), alongside hepatitis D virus (HDV) super-/co-infection and chronic hepatitis C (HCV), are major contributors to cirrhosis, end-stage liver disease, hepatocellular carcinoma (HCC), and liver-related mortality. Despite significant progress in antiviral treatments and HBV vaccination, viral hepatitis remains a global [...] Read more.
Chronic hepatitis B (HBV), alongside hepatitis D virus (HDV) super-/co-infection and chronic hepatitis C (HCV), are major contributors to cirrhosis, end-stage liver disease, hepatocellular carcinoma (HCC), and liver-related mortality. Despite significant progress in antiviral treatments and HBV vaccination, viral hepatitis remains a global health burden. Vulnerable populations, such as those experiencing homelessness, migrants, and economically disadvantaged groups, are disproportionately impacted by these infections, often facing barriers to care and exclusion from traditional health systems. This leads to undiagnosed cases and ongoing transmission, undermining global efforts to eliminate HBV and HCV by 2030, as outlined by the World Health Organization (WHO). Recent studies highlight the importance of tailored interventions to address health inequalities. For instance, on-site community-based screening initiatives targeting marginalized groups have shown promise, achieving higher linkage to care rates without monetary incentives. These approaches not only enhance diagnosis but also facilitate integration into healthcare systems, addressing both public health and social disparities. This review underscores the need for targeted strategies to promote the early detection and management of HBV and HCV in underserved populations. Such efforts are critical to advancing the WHO’s elimination goals, improving health outcomes, and addressing the broader social determinants of health. Full article
18 pages, 1010 KiB  
Review
Asian Perspective on Hepatitis B Virus and Hepatitis C Virus Elimination
by Apichat Kaewdech, Phunchai Charatcharoenwitthaya and Teerha Piratvisuth
Viruses 2025, 17(1), 34; https://doi.org/10.3390/v17010034 - 29 Dec 2024
Viewed by 1625
Abstract
Hepatitis B virus (HBV) and hepatitis C virus (HCV) infections remain significant public health challenges in Asia, affecting millions and contributing to substantial morbidity and mortality. The prevalence of these infections varies across the region, with factors such as vaccination coverage, healthcare infrastructure, [...] Read more.
Hepatitis B virus (HBV) and hepatitis C virus (HCV) infections remain significant public health challenges in Asia, affecting millions and contributing to substantial morbidity and mortality. The prevalence of these infections varies across the region, with factors such as vaccination coverage, healthcare infrastructure, and sociocultural barriers influencing the epidemiology of both viruses. The persistent burden of chronic HBV, particularly in older populations, and the evolving HCV genotype landscape highlight the need for targeted, region-specific strategies. Universal screening programs have emerged as essential tools for detecting undiagnosed cases and optimizing healthcare resource allocation. Given the overlapping epidemiology of HBV and HCV, comprehensive public health interventions tailored to the unique contexts of different Asian countries are crucial for achieving global elimination goals. This review examines the epidemiological trends, challenges, and opportunities for addressing HBV and HCV in Asia, emphasizing the importance of overcoming sociocultural barriers to improve prevention, diagnosis, and treatment efforts across diverse populations. Full article
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15 pages, 1052 KiB  
Review
Two Concepts of Hepatitis B Core-Related Antigen Assay: A Highly Sensitive and Rapid Assay or an Effective Tool for Widespread Screening
by Takako Inoue, Shintaro Yagi and Yasuhito Tanaka
Viruses 2024, 16(6), 848; https://doi.org/10.3390/v16060848 - 26 May 2024
Cited by 1 | Viewed by 2305
Abstract
Hepatitis B core-related antigen (HBcrAg) reflects the activity of intrahepatic covalently closed circular DNA. HBcrAg can be detected even in chronic hepatitis B patients in whom serum HBV DNA or hepatitis B surface antigen is undetectable. The HBcrAg measurement system was developed based [...] Read more.
Hepatitis B core-related antigen (HBcrAg) reflects the activity of intrahepatic covalently closed circular DNA. HBcrAg can be detected even in chronic hepatitis B patients in whom serum HBV DNA or hepatitis B surface antigen is undetectable. The HBcrAg measurement system was developed based on two concepts. One is a fully-automated and highly-sensitive HBcrAg assay (iTACT-HBcrAg) and the other is a point-of-care testing (POCT) that can be used in in resource-limited areas. iTACT-HBcrAg is an alternative to HBV DNA for monitoring HBV reactivation and predicting the development of hepatocellular carcinoma. This validated biomarker is available in routine clinical practice in Japan. Currently, international guidelines for the prevention of mother-to-child transmission recommend anti-HBV prophylaxis for pregnant women with high viral loads. However, over 95% of HBV-infected individuals live in countries where HBV DNA quantification is widely unavailable. Given this situation, a rapid and simple HBcrAg assay for POCT would be highly effective. Long-term anti-HBV therapy may have potential side effects and appropriate treatment should be provided to eligible patients. Therefore, a simple method of determining the indication for anti-HBV treatment would be ideal. This review provides up-to-date information regarding the clinical value of HBcrAg in HBV management, based on iTACT-HBcrAg or POCT. Full article
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