Evidence map›Paper›PMID 31645650›Full record

ArticleScientific reports2019

In silico/In vivo analysis of high-risk papillomavirus L1 and L2 conserved sequences for development of cross-subtype prophylactic vaccine.

Ali Namvar, Azam Bolhassani, Gholamreza Javadi, Zahra Noormohammadi

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Immune Responses to Human Papillomavirus After Infection and Vaccination.Current topics in microbiology and immunology · 2026
    Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Current and future direction in treatment of HPV-related cervical disease.Journal of molecular medicine (Berlin, Germany) · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. A Comprehensive in Silico Analysis for Identification of Immunotherapeutic Epitopes of HPV-18.International journal of peptide research and therapeutics · 2021
    Article
  15. Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Ali NamvarDepartment of Biology, School of Basic Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Azam BolhassaniDepartment of Hepatitis and AIDS, Pasteur Institute of Iran, Tehran, Iran. A_bolhasani@pasteur.ac.ir.
Gholamreza JavadiDepartment of Biology, School of Basic Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Zahra NoormohammadiDepartment of Biology, School of Basic Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human papillomavirus (HPV) is the most common sexually transmitted infection in the world and the main cause of cervical cancer. Nowadays, the virus-like particles (VLPs) based on L1 proteins have been considered as the best candidate for vaccine development against HPV infections. Two commercial HPV (Gardasil and Cervarix) are available. These HPV VLP vaccines induce genotype-limited protection. The major impediments such as economic barriers especially gaps in financing obstructed the optimal delivery of vaccines in developing countries. Thus, many efforts are underway to develop the next generation of vaccines against other types of high-risk HPV. In this study, we developed DNA constructs (based on L1 and L2 genes) that were potentially immunogenic and highly conserved among the high-risk HPV types. The framework of analysis include (1) B-cell epitope mapping, (2) T-cell epitope mapping (i.e., CD4

Indexed as

Amino Acid SequenceAnimalsCapsid ProteinsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesConserved SequenceEpitope MappingEpitopesFemaleHEK293 CellsHuman papillomavirus 16Human papillomavirus 18HumansMice, Inbred C57BLOncogene Proteins, ViralPapillomavirus InfectionsCapsid ProteinsEpitopesL1 protein, Human papillomavirus type 16L2 protein, Human papillomavirus type 16Oncogene Proteins, ViralPapillomavirus VaccinesVaccines, Virus-Like Particle

Identifiers

PMID31645650
PMCPMC6811573

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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 OpenQuestion graph.