Evidence map›Paper›PMID 35681036›Full record

ArticleScientific reports2022

Designing of multi-epitope chimeric vaccine using immunoinformatic platform by targeting oncogenic strain HPV 16 and 18 against cervical cancer.

Anoop Kumar, Utkarsha Sahu, Pratima Kumari, Anshuman Dixit, Prashant Khare

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

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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 2 institutions in 1 country.

Anoop KumarNational Institute of Biologicals (NIB), Noida, Uttar Pradesh, India.
Utkarsha SahuDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, 462020, India.
Pratima KumariInstitute of Life Science, Nalco Square, Bhubaneswar, Odisha, 751023, India.
Anshuman DixitInstitute of Life Science, Nalco Square, Bhubaneswar, Odisha, 751023, India.
Prashant KhareDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, 462020, India. pacifickhare@gmail.com.
Institute of Life Sciences · INAll India Institute of Medical Sciences Bhopal · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer is the most common gynaecological cancer and reaches an alarming stage. HPVs are considered the main causative agents for cervical cancer and other sexually transmitted infections across the globe. Currently, three prophylactic vaccines are available against HPV infections with no therapeutic values. Due to a lack of effective therapeutic and prophylactic measures, the HPV infection is spreading in an uncontrolled manner. Next-generation of vaccine is needed to have both prophylactic and therapeutic values against HPV. Here first time we have designed a multi-epitope chimeric vaccine using the most oncogenic strain HPV 16 and HPV 18 through an immunoinformatic approach. In this study, we have used the L1, E5, E6 and E7 oncoproteins from both HPV 16 and HPV 18 strains for epitope prediction. Our recombinant chimeric vaccine construct consists, selected helper and cytotoxic T cell epitopes. Our computational analysis suggests that this chimeric construct is highly stable, non-toxic and also capable of inducing both cell-mediated and humoral immune responses. Furthermore, in silico cloning of the multi-epitope chimeric vaccine construct was done and the stabilization of the vaccine construct is validated with molecular dynamics simulation studies. Finally, our results indicated that our construct could be used for an effective prophylactic and therapeutic vaccine against HPV.

Indexed as

Oncogene Proteins, ViralPapillomavirus InfectionsPapillomavirus VaccinesUterine Cervical NeoplasmsEpitopes, T-LymphocyteFemaleHuman papillomavirus 16Human papillomavirus 18HumansPapillomaviridaeVaccines, SyntheticEpitopes, T-LymphocyteOncogene Proteins, ViralPapillomavirus VaccinesVaccines, Synthetic

Identifiers

PMID35681036
PMCPMC9184633
OpenAlexW4282938499

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.