Evidence map›Paper›PMID 40619783›Full record

ReviewJournal of biosciences2025

Human papillomavirus vaccine: Success and challenges.

Chamma Gupta, Karma G Dolma, Mingma L Sherpa, Arundhati Bag, Abhishek Byahut

Abstract readReview
PubMed
In one paragraph

Review in Journal of biosciences, 2025. 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
–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

2 citing papers in PubMed.

  1. Review
  2. Review
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.

Chamma GuptaDepartment of Biochemistry, Sikkim Manipal Institute of Medical Sciences, Sikkim Manipal University, Gangtok 737102, Sikkim, India.
Karma G Dolma
Mingma L Sherpa
Arundhati Bag
Abhishek Byahut

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistent infection with high-risk human papillomavirus (HPV) is a major etiological cause of cancers associated with the cervix, anogenital region, vulva, vagina, penis, and oropharynx. Cervarix®, Gardasil®, and Gardsil9® are three approved prophylactic vaccines that can effectively provide protection against HPV infection. However,they only offer protection against a limited number of HPV strains, not all of which can cause cervical cancer (CC). Additionally, they only provide limited therapeutic advantages against HPV infections that have already been established. Thus, developing a therapeutic vaccine is urgently required and is the need of the hour. Unlike normal cells, two of the viral early proteins, E6 and E7, are persistently expressed in tumor cells. This makes these two proteins the prime candidates for therapeutic vaccines that aim to eliminate the infected cells by cytotoxic T-lymphocytes without affecting normal cells. Therapeutic vaccinations are being researched and are under trials, and no such vaccines have yet been authorized. The development of a therapeutic vaccination coupled with currently available prophylactic vaccines is anticipated to significantly lower morbidity and cancer load globally. This review aims to provide a clear understanding of the molecular basis, immunogenicity, effectiveness, and challenges of current prophylactic vaccines and the future scope of implementing therapeutic vaccines against infection caused by HPV.

Indexed as

PapillomaviridaePapillomavirus InfectionsPapillomavirus VaccinesUterine Cervical NeoplasmsFemaleHumansOncogene Proteins, ViralPapillomavirus E7 ProteinsOncogene Proteins, ViralPapillomavirus E7 ProteinsPapillomavirus Vaccines

Identifiers

PMID40619783

What OpenQuestion holds

Textmetadata
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.