Evidence map›Paper›PMID 35668533›Full record

ArticleJournal of experimental & clinical cancer research : CR2022

Linear DNA amplicons as a novel cancer vaccine strategy.

Antonella Conforti, Erika Salvatori, Lucia Lione, Mirco Compagnone, Eleonora Pinto, Clay Shorrock, James A Hayward, Yuhua Sun, Ben Minghwa Liang, Fabio Palombo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 17 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

12 authors at 3 institutions in 2 countries.

Antonella ConfortiTakis, Via Castel Romano 100, 00128, Rome, Italy. conforti@evvivax.com.ORCID http://orcid.org/0000-0001-8524-5936
Erika SalvatoriTakis, Via Castel Romano 100, 00128, Rome, Italy.
Lucia LioneTakis, Via Castel Romano 100, 00128, Rome, Italy.
Mirco CompagnoneNeomatrix, Via Castel Romano 100, 00128, Rome, Italy.
Eleonora PintoTakis, Via Castel Romano 100, 00128, Rome, Italy.
Clay ShorrockApplied DNA Sciences, 50 Health Sciences Drive, Stony Brook, NY, 11790, USA.
James A HaywardApplied DNA Sciences, 50 Health Sciences Drive, Stony Brook, NY, 11790, USA.
Yuhua SunApplied DNA Sciences, 50 Health Sciences Drive, Stony Brook, NY, 11790, USA.
Ben Minghwa LiangApplied DNA Sciences, 50 Health Sciences Drive, Stony Brook, NY, 11790, USA.
Fabio PalomboTakis, Via Castel Romano 100, 00128, Rome, Italy. palombo@neomatrixbiotech.com.
Brian ViscountApplied DNA Sciences, 50 Health Sciences Drive, Stony Brook, NY, 11790, USA. brian.viscount@adnas.com.
Luigi AurisicchioTakis, Via Castel Romano 100, 00128, Rome, Italy. aurisicchio@evvivax.com.
Applied DNA Sciences (United States) · USRINA Consulting - Centro Sviluppo Materiali S.p.A. (Italy) · ITNeuroMetrix (United States) · US

Funding

Ministero dello Sviluppo Economico F/190180/01/X44Regione Campania B61G18000470007
6 · The paper itself

Abstract

backgroundDNA-based vaccines represent a simple, safe and promising strategy for harnessing the immune system to fight infectious diseases as well as various forms of cancer and thus are considered an important tool in the cancer immunotherapy toolbox. Nonetheless, the manufacture of plasmid DNA vaccines has several drawbacks, including long lead times and the need to remove impurities from bacterial cultures. Here we report the development of polymerase chain reaction (PCR)-produced amplicon expression vectors as DNA vaccines and their in vivo application to elicit antigen-specific immune responses in animal cancer models.

methodsPlasmid DNA and amplicon expression was assessed both in vitro, by Hela cells transfection, and in vivo, by evaluating luciferase expression in wild-type mice through optical imaging. Immunogenicity induced by DNA amplicons was assessed by vaccinating wild-type mice against a tumor-associated antigen, whereas the antitumoral effect of DNA amplicons was evaluated in a murine cancer model in combination with immune-checkpoint inhibitors (ICIs).

resultsAmplicons encoding tumor-associated-antigens, such as telomerase reverse transcriptase or neoantigens expressed by murine tumor cell lines, were able to elicit antigen-specific immune responses and proved to significantly impact tumor growth when administered in combination with ICIs.

conclusionsThese results strongly support the further exploration of the use of PCR-based amplicons as an innovative immunotherapeutic approach to cancer treatment.

Indexed as

Cancer VaccinesNeoplasmsVaccines, DNAAnimalsAntigens, NeoplasmDNAHeLa CellsHumansImmunotherapyMiceAntigens, NeoplasmCancer VaccinesDNAVaccines, DNAAmpliconsCancer immunotherapyDNA vaccinePCR

Identifiers

PMID35668533
PMCPMC9169303
OpenAlexW4281759798

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.