Evidence map›Paper›PMID 28780375›Full record

ReviewClinical immunology (Orlando, Fla.)2017

Adjuvant formulations for virus-like particle (VLP) based vaccines.

Velasco Cimica, Jose M Galarza

Abstract readReview
In one paragraph

Review in Clinical immunology (Orlando, Fla.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
–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

77 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  20. A review on Zika vaccine development.Pathogens and disease · 2024
    Review

17 more citing papers are in PubMed but not listed here.

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

2 authors.

Velasco CimicaTechnoVax, Inc., 765 Old Saw Mill River Road, Tarrytown, NY 10591, United States.
Jose M GalarzaTechnoVax, Inc., 765 Old Saw Mill River Road, Tarrytown, NY 10591, United States. Electronic address: jmgalarza@technovax.com.

Funding

Development, Production and Testing of VLP based Respiratory Syncytial Virus (RSVR43AI108099 · NIAID · TECHNOVAX, INC. · PI GALARZA, JOSE M. · 2014 to 2014
$510k
NIAID NIH HHS R43 AI108099
6 · The paper itself

Abstract

The development of virus-like particle (VLP) technology has had an enormous impact on modern vaccinology. In order to optimize the efficacy and safety of VLP-based vaccines, adjuvants are included in most vaccine formulations. To date, most licensed VLP-based vaccines utilize the classic aluminum adjuvant compositions. Certain challenging pathogens and weak immune responder subjects may require further optimization of the adjuvant formulation to maximize the magnitude and duration of the protective immunity. Indeed, novel classes of adjuvants such as liposomes, agonists of pathogen recognition receptors, polymeric particles, emulsions, cytokines and bacterial toxins, can be used to further improve the immunostimulatory activity of a VLP-based vaccine. This review describes the current advances in adjuvant technology for VLP-based vaccines directed at viral diseases, and discusses the basic principles for designing adjuvant formulations for enhancing the vaccine immunogenicity.

Indexed as

Adjuvants, ImmunologicBacterial ToxinsCytokinesDrug CompoundingDrug DiscoveryHumansImmunogenicity, VaccineLiposomesPolymersVaccines, Virus-Like ParticleAdjuvants, ImmunologicBacterial ToxinsCytokinesLiposomesPolymersVaccines, Virus-Like Particle

Identifiers

PMID28780375
PMCPMC5673579

What OpenQuestion holds

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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.