Evidence map›Paper›PMID 27471642›Full record

ArticleOncoimmunology2016

A plant-expressed conjugate vaccine breaks CD4(+) tolerance and induces potent immunity against metastatic Her2(+) breast cancer.

Warayut Chotprakaikiat, Alex Allen, Duc Bui-Minh, Elena Harden, Jantipa Jobsri, Federica Cavallo, Yuri Gleba, Freda K Stevenson, Christian Ottensmeier, Victor Klimyuk and 1 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2016. 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
4.6field-weighted citation impact, top 6% 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, 40 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

11 authors at 3 institutions in 3 countries.

Warayut ChotprakaikiatCancer Sciences Unit, Faculty of Medicine, University of Southampton , Southampton, UK.
Alex AllenCancer Sciences Unit, Faculty of Medicine, University of Southampton , Southampton, UK.
Duc Bui-MinhIcon Genetics , Halle, Germany.
Elena HardenCancer Sciences Unit, Faculty of Medicine, University of Southampton , Southampton, UK.
Jantipa JobsriOral Biology Department, Naresuan University , Phitsanulok, Thailand.
Federica CavalloDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Turin , Turin, Italy.
Yuri GlebaIcon Genetics , Halle, Germany.
Freda K StevensonCancer Sciences Unit, Faculty of Medicine, University of Southampton , Southampton, UK.
Christian OttensmeierCancer Sciences Unit, Faculty of Medicine, University of Southampton , Southampton, UK.
Victor KlimyukIcon Genetics , Halle, Germany.
Natalia SavelyevaCancer Sciences Unit, Faculty of Medicine, University of Southampton , Southampton, UK.
University of Southampton · GBNaresuan University · THUniversity of Turin · IT

Funding

Cancer Research UK 15951Cancer Research UK 18158Cancer Research UK 18161Cancer Research UK 18892Cancer Research UK 20613Cancer Research UK 22795
6 · The paper itself

Abstract

Passive antibody therapy for cancer is an effective but costly treatment modality. Induction of therapeutically potent anticancer antibodies by active vaccination is an attractive alternative but has proven challenging in cancer due to tolerogenic pressure in patients. Here, we used the clinically relevant cancer target Her2, known to be susceptible to targeting by antibody therapy, to demonstrate how potent antibody can be induced by vaccination. A novel 44kD Her2 protein fragment was generated and found to be highly effective at inducing anti-Her2 antibody including trastuzumab-like reactivities. In the tolerant and spontaneous BALB-neuT mouse model of metastatic breast cancer this Her2-targeting vaccine was only effective if the fragment was conjugated to a foreign immunogenic carrier; Fragment C of tetanus toxin. Only the conjugate vaccine induced high affinity anti-Her2 antibody of multiple isotypes and suppressed tumor development. The magnitude of CD4(+) T-cell help and breadth of cytokines secreted by the CD4(+) T helper (Th) cells induced to the foreign antigen was critical. We used a highly efficient plant-based bio-manufacturing process for protein antigens, magnICON, for vaccine expression, to underpin feasibility of future clinical testing. Hence, our novel Her2-targeting conjugate vaccine combines preclinical efficacy with clinical deliverability, thus setting the scene for therapeutic testing.

Indexed as

Antibodybreast cancerCD4+ T helper cellsplant-based bio-manufacturingvaccines

Identifiers

PMID27471642
PMCPMC4938312
OpenAlexW2341538992

What OpenQuestion holds

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LicenceCC BY
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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.