Evidence map›Paper›PMID 33478147›Full record

ArticleVaccines2021

A Scalable Manufacturing Approach to Single Dose Vaccination against HPV.

Shuai Shao, Oscar A Ortega-Rivera, Sayoni Ray, Jonathan K Pokorski, Nicole F Steinmetz

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Recent advancements in single dose slow-release devices for prophylactic vaccines.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2023
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. 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 at 1 institution in 1 country.

Shuai ShaoDepartment of NanoEngineering, University of California San Diego, La Jolla, CA 92093, USA.
Oscar A Ortega-RiveraDepartment of NanoEngineering, University of California San Diego, La Jolla, CA 92093, USA.ORCID 0000-0002-0773-0677
Sayoni RayDepartment of NanoEngineering, University of California San Diego, La Jolla, CA 92093, USA.ORCID 0000-0002-1947-181X
Jonathan K PokorskiDepartment of NanoEngineering, University of California San Diego, La Jolla, CA 92093, USA.ORCID 0000-0001-5869-6942
Nicole F SteinmetzDepartment of NanoEngineering, University of California San Diego, La Jolla, CA 92093, USA.ORCID 0000-0002-0130-0481
University of California San Diego · US

Funding

Protein/Polymer Devices for Slow-Release of Immunotherapies to Treat Ovarian CancerR21EB024874 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI POKORSKI, JONATHAN KYLE, STEINMETZ, NICOLE FRANZISKA · 2017 to 2018
$431k
National Science Foundation CMMI- 2027668NIH HHS R21EB024874UC MEXUS-CONACYT FE-19-58
6 · The paper itself

Abstract

Human papillomavirus (HPV) is a globally prevalent sexually-transmitted pathogen, responsible for most cases of cervical cancer. HPV vaccination rates remain suboptimal, partly due to the need for multiple doses, leading to a lack of compliance and incomplete protection. To address the drawbacks of current HPV vaccines, we used a scalable manufacturing process to prepare implantable polymer-protein blends for single-administration with sustained delivery. Peptide epitopes from HPV16 capsid protein L2 were conjugated to the virus-like particles derived from bacteriophage Qβ, to enhance their immunogenicity. The HPV-Qβ particles were then encapsulated into poly(lactic-co-glycolic acid) (PLGA) implants, using a benchtop melt-processing system. The implants facilitated the slow and sustained release of HPV-Qβ particles without the loss of nanoparticle integrity, during high temperature melt processing. Mice vaccinated with the implants generated IgG titers comparable to the traditional soluble injections and achieved protection in a pseudovirus neutralization assay. HPV-Qβ implants offer a new vaccination platform; because the melt-processing is so versatile, the technology offers the opportunity for massive upscale into any geometric form factor. Notably, microneedle patches would allow for self-administration in the absence of a healthcare professional, within the developing world. The Qβ technology is highly adaptable, allowing the production of vaccine candidates and their delivery devices for multiple strains or types of viruses.

Indexed as

hot melt extrusionHPV vaccine candidateL2 proteinPLGA implantsQβvaccine delivery devicevirus-like particles (VLPs)

Identifiers

PMID33478147
PMCPMC7835769
OpenAlexW3122250862

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.