Evidence map›Paper›PMID 25689082›Full record

ArticleBiotechnology and bioengineering2015

Influenza virus-like particles engineered by protein transfer with tumor-associated antigens induces protective antitumor immunity.

Jaina M Patel, Vincent F Vartabedian, Min-Chul Kim, Sara He, Sang-Moo Kang, Periasamy Selvaraj

Erratum issuedAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 48 citations in OpenAlex.

  1. Cancer/Testis Antigens as Targets for RNA-Based Anticancer Therapy.International journal of molecular sciences · 2023
    Review
  2. Virus-like Particle (VLP) Vaccines for Cancer Immunotherapy.International journal of molecular sciences · 2023
    Review
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  13. Nanoparticle-mediated targeted drug delivery for breast cancer treatment.Biochimica et biophysica acta. Reviews on cancer · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Jaina M PatelDepartment of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, 30322, Georgia.
Vincent F Vartabedian
Min-Chul Kim
Sara He
Sang-Moo Kang
Periasamy Selvaraj
Emory University · USAnimal and Plant Quarantine Agency · KRGeorgia State University · US

Funding

Influenza vaccines inducing broadly cross protective immunityR01AI093772 · NIAID · GEORGIA STATE UNIVERSITY · PI KANG, SANG-MOO · 2011 to 2020
$4.2M
VLP Vaccine TechnologyR01AI105170 · NIAID · GEORGIA STATE UNIVERSITY · PI KANG, SANG-MOO · 2013 to 2017
$3.7M
Glycolipid-anchored cytokines as breast cancer membrane vaccine adjuvantsR01CA138993 · NCI · EMORY UNIVERSITY · PI SELVARAJ, PERIASAMY · 2009 to 2013
$1.6M
Tumor antigen-decorated virus-like particles as a therapeutic cancer vaccineF31CA165632 · NCI · EMORY UNIVERSITY · PI PATEL, JAINA · 2012 to 2014
$84k
NCI NIH HHS 1-F31-CA165632NCI NIH HHS 1-R01-CA138993NCI NIH HHS F31 CA165632NCI NIH HHS R01 CA138993NIAID NIH HHS R01 AI093772NIAID NIH HHS R01-AI093772NIAID NIH HHS R01 AI105170NIAID NIH HHS R01-AI105170
6 · The paper itself

Abstract

Delivery of antigen in particulate form using either synthetic or natural particles induces stronger immunity than soluble forms of the antigen. Among naturally occurring particles, virus-like particles (VLPs) have been genetically engineered to express tumor-associated antigens (TAAs) and have shown to induce strong TAA-specific immune responses due to their nano-particulate size and ability to bind and activate antigen-presenting cells. In this report, we demonstrate that influenza VLPs can be modified by a protein transfer technology to express TAAs for induction of effective antitumor immune responses. We converted the breast cancer HER-2 antigen to a glycosylphosphatidylinositol (GPI)-anchored form and incorporated GPI-HER-2 onto VLPs by a rapid protein transfer process. Expression levels on VLPs depended on the GPI-HER-2 concentration added during protein transfer. Vaccination of mice with protein transferred GPI-HER-2-VLPs induced a strong Th1 and Th2-type anti-HER-2 antibody response and protected mice against a HER-2-expressing tumor challenge. The Soluble form of GPI-HER-2 induced only a weak Th2 response under similar conditions. These results suggest that influenza VLPs can be enriched with TAAs by protein transfer to develop effective VLP-based subunit vaccines against cancer without chemical or genetic modifications and thus preserve the immune stimulating properties of VLPs for easier production of antigen-specific therapeutic cancer vaccines.

Indexed as

Drug CarriersAnimalsAntibodies, NeoplasmAntigens, NeoplasmCancer VaccinesDisease Models, AnimalErb-b2 Receptor Tyrosine KinasesHumansImmunityMiceNeoplasmsOrthomyxoviridaeVaccines, Virus-Like ParticleAntibodies, NeoplasmAntigens, NeoplasmCancer VaccinesDrug CarriersERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesVaccines, Virus-Like Particlebreast cancerHER-2protein transfervaccinevirus-like particles

Identifiers

PMID25689082
PMCPMC4621003
OpenAlexW1617101517

What OpenQuestion holds

Textmetadata
LicenceTDM
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.