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Adenovirus
Abstract
Adenoviruses (AdV) are DNA viruses that typically cause mild infections involving the upper or lower respiratory tract, gastrointestinal (GI) tract, or conjunctiva. Rare manifestations of AdV infections include hemorrhagic cystitis, hepatitis, hemorrhagic colitis, pancreatitis, nephritis, or encephalitis. Adenovirus infections are more common in young children, owing to lack of humoral immunity. Epidemics of AdV infections may occur in healthy children or adults in closed or crowded settings (particularly military recruits). The disease is more severe, and dissemination is more likely in patients with impaired immunity (eg, organ transplant recipients, human immunodeficiency virus infection, congenital immunodeficiency syndromes). Fatality rates for untreated severe AdV pneumonia or disseminated disease may exceed 50%. More than 50 serotypes of AdV have been identified. Different serotypes display different tissue trophisms and correlate with clinical manifestations of infection. The predominant serotypes differ among countries or regions and change over time. Transmission of novel strains between countries or across continents and replacement of dominant serotypes by new strains may occur. Treatment of AdV infections is controversial because prospective, randomized therapeutic trials have not been done. Cidofovir is considered the drug of choice for severe AdV infections, but not all patients require treatment. Vaccines have been shown to be highly efficacious in reducing the risk of respiratory AdV infection but are currently not available.
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One major drawback of the Ad vector is the potential immune responses it may induce, as Ad is known to cause respiratory and other kinds of infections in humans and animals.
“However, one of the major drawbacks of the Ad vector is the potential immune responses it may induce, as Ad is known to cause respiratory and other kinds of infections in humans and animals [62].”
From Immune responses to gene editing by viral and non-viral delivery vectors used in retinal gene therapy (2022) · cites this paper as [62]
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Ren, D., Fisson, S., Dalkara, D., & Ail, D. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14091973 · Cited by 52
Metadata
- Authors
- Lynch, J., Fishbein, M., & Echavarria, M.
- Affiliations
- University of California, Los Angeles (US)
- ORCID
- Fishbein, Michael
- Venue
- Seminars in Respiratory and Critical Care Medicine
- Publisher
- Georg Thieme Verlag KG
- Published
- 2011-08
- Volume
- 32
- Issue
- 04
- Pages
- 494-511
- ISSN
- 1069-3424 (ISSN-L)
- 1098-9048
- OpenAlex
- W4240713867
- Cited by
- 301
- References
- 0
- Citations by year
- 2026: 12 · 2025: 35 · 2024: 34 · 2023: 28 · 2022: 19 · 2021: 31 · 2020: 18 · 2019: 8 · 2018: 16 · 2017: 14 · 2016: 22 · 2015: 13 · 2014: 17 · 2013: 17 · 2012: 16
- FWCI
- 12.05
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Seminars in Respiratory and Critical Care Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Respiratory viral infections research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Health Sciences › Medicine › Epidemiology › Cytomegalovirus and herpesvirus research
- Keywords
- adenovirus infection, adenovirus pneumonia, hemorrhagic cystitis, adenovirus serotypes, immunocompromised patients, cidofovir, adenovirus vaccine, respiratory infections, disseminated adenovirus infection
- MeSH terms
- Cidofovir, Adenoviridae, Adenoviridae Infections, Adult, Age Factors, Antiviral Agents, Child, Cytosine, Humans, Serotyping, Severity of Illness Index, Organophosphonates
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