Evidence map›Paper›PMID 39180020›Full record

ReviewVirology journal2024

From discovery to treatment: tracing the path of hepatitis E virus.

Arash Letafati, Zahra Taghiabadi, Mahshid Roushanzamir, Bahar Memarpour, Saba Seyedi, Ali Vasheghani Farahani, Masoomeh Norouzi, Saeideh Karamian, Arghavan Zebardast, Marzieh Mehrabinia and 5 more

Erratum issuedAbstract readReview
In one paragraph

Review in Virology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Arash Letafati *Department of Virology, Faculty of Public Health, Tehran University of Medical Sciences, Tehran, Iran. arashletafati@yahoo.com.
Zahra Taghiabadi *Research Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Mahshid RoushanzamirResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Bahar MemarpourResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Saba SeyediResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Ali Vasheghani FarahaniResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Masoomeh NorouziResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Saeideh KaramianResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Arghavan ZebardastResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Marzieh MehrabiniaResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Omid Salahi ArdekaniResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Tina FallahResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Fatemeh KhazryResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Samin Fathi DaneshvarResearch Center for Clinical Virology, Tehran University of Medical Science, Tehran, Iran.
Mehdi NorouziDepartment of Virology, Faculty of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hepatitis E virus (HEV) is a major cause of acute viral hepatitis worldwide. HEV is classified into eight genotypes, labeled HEV-1 through HEV-8. Genotypes 1 and 2 exclusively infect humans, while genotypes 3, 4, and 7 can infect both humans and animals. In contrast, genotypes 5, 6, and 8 are restricted to infecting animals. While most individuals with a strong immune system experience a self-limiting infection, those who are immunosuppressed may develop chronic hepatitis. Pregnant women are particularly vulnerable to severe illness and mortality due to HEV infection. In addition to liver-related complications, HEV can also cause extrahepatic manifestations, including neurological disorders. The immune response is vital in determining the outcome of HEV infection. Deficiencies in T cells, NK cells, and antibody responses are linked to poor prognosis. Interestingly, HEV itself contains microRNAs that regulate its replication and modify the host's antiviral response. Diagnosis of HEV infection involves the detection of HEV RNA and anti-HEV IgM/IgG antibodies. Supportive care is the mainstay of treatment for acute infection, while chronic HEV infection may be cleared with the use of ribavirin and pegylated interferon. Prevention remains the best approach against HEV, focusing on sanitation infrastructure improvements and vaccination, with one vaccine already licensed in China. This comprehensive review provides insights into the spread, genotypes, prevalence, and clinical effects of HEV. Furthermore, it emphasizes the need for further research and attention to HEV, particularly in cases of acute hepatitis, especially among solid-organ transplant recipients.

Indexed as

GenotypeHepatitis EHepatitis E virusAnimalsAntiviral AgentsHumansAntiviral AgentsHEVPathogenesisPrevalenceTransmissionTreatment

Identifiers

PMID39180020
PMCPMC11342613

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.