Evidence map›Paper›PMID 35901328›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2022

Dissection of Capsid Protein HPV 52 to Rationalize Vaccine Designs Using Computational Approaches Immunoinformatics and Molecular Docking.

Moh Egy Rahman Firdaus, Apon Zaenal Mustopa, Lita Triratna, Gita Syahputra, Maritsa Nurfatwa

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 36% of its field
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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 1 institution in 1 country.

Moh Egy Rahman FirdausResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor, 16911, West Java, Indonesia.ORCID https://orcid.org/00
Apon Zaenal MustopaResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor, 16911, West Java, Indonesia.ORCID 0000-0001-6614-5518
Lita TriratnaResearch Center for Applied Zoology, National Research and Innovation Agency (BRIN), Bogor, 16911, West Java, Indonesia.
Gita SyahputraResearch Center for Vaccine and Drug, National Research and Innovation Agency (BRIN), Bogor, 16911, West Java, Indonesia.
Maritsa NurfatwaResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor, 16911, West Java, Indonesia.
Indonesian Agency for Agricultural Research and Development · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman Papillomavirus type 52 (HPV 52) is considered one of the threatening HPV types inducing cervical cancer worldwide. This study was conducted to address strategies of an effective vaccine against cervical cancer using computational approaches immuno-informatics and molecular docking.

methodsMajor capsid protein L1 and L2 HPV 52 (L1 and L2 HPV 52) sequences were investigated by multiple analyses including B and T cell epitope, toxicity, allergenicity, Immunogenicity, epitope conservancy, population coverage, and molecular docking.

resultsL1 and L2 HPV 52 showed a conserved sequence among amino acid levels. Q307K, S383D/N, and D473E are found as major mutations in L1, while mutations in L2 are S122T, Q247H, L247S, and E365D. Multiple epitopes were identified and elicited strong immune responses against cross types of HPV in various HLA populations. To enhance vaccine effectiveness that allows having cross-protection over HPV types, N terminus HPV L2 was analyzed suggesting multi-candidates chimeric L1/L2 vaccine design.

conclusionThis study shed a light on a useful pipeline with robust analysis for effective vaccine production.

Indexed as

Oncogene Proteins, ViralPapillomavirus InfectionsPapillomavirus VaccinesUterine Cervical NeoplasmsCapsid ProteinsEpitopes, T-LymphocyteFemaleHumansMolecular Docking SimulationPapillomaviridaeCapsid ProteinsEpitopes, T-LymphocyteOncogene Proteins, ViralPapillomavirus VaccinesHPV 52Immuno-informaticsL1L2multi-epitope vaccine

Identifiers

PMID35901328
PMCPMC9727352
OpenAlexW4288388807

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.