Evidence map›Paper›PMID 26689376›Full record

ArticleNature nanotechnology2016

In situ vaccination with cowpea mosaic virus nanoparticles suppresses metastatic cancer.

P H Lizotte, A M Wen, M R Sheen, J Fields, P Rojanasopondist, N F Steinmetz, S Fiering

Abstract read
In one paragraph

Article in Nature nanotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 259 papers.

0numbers the graph read from it
0cells of the map it votes in
259citing papers in PubMed
–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

259 citing papers in PubMed.

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  11. Trojan Horse Strategy: How Biomimetic Nanomedicine Remodels the Tumor Microenvironment.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  12. Article
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199 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

P H LizotteDepartment of Microbiology and Immunology, The Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire 03756, USA.
A M WenBiomedical Engineering, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, USA.
M R SheenDepartment of Microbiology and Immunology, The Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire 03756, USA.
J FieldsDepartment of Microbiology and Immunology, The Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire 03756, USA.
P RojanasopondistDepartment of Microbiology and Immunology, The Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire 03756, USA.
N F SteinmetzBiomedical Engineering, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, USA.
S FieringDepartment of Microbiology and Immunology, The Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire 03756, USA.

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
Toxicology, Pathology and Biodistribution Core (TPB Core)U54CA151662 · NCI · DARTMOUTH COLLEGE · PI DEMIDENKO, EUGENE · 2010 to 2014
$11.6M
IMMUNOBIOLOGY OF MYELOID AND LYMPHOID CELLST32AI007363 · NIAID · DARTMOUTH COLLEGE · PI Claudia V Jakubzick · 1990 to 2026
$9.5M
Center for Molecular, Cellular, and Translational ImmunologyP30GM103415 · NIGMS · DARTMOUTH COLLEGE · PI GREEN, WILLIAM R · 2012 to 2015
$4.7M
Cardiovascular Research Training Program (CRTP)T32HL105338 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI JAIN, MUKESH KUMAR · 2010 to 2014
$1.8M
CENTER FOR MOLECULAR, CELLULAR, AND TRANSLATIONAL IMMUNOLOGYP30RR032136 · NCRR · DARTMOUTH COLLEGE · PI GREEN, WILLIAM R · 2011 to 2011
$1.2M
NCI NIH HHS NIH 1 U54 CA151662NCI NIH HHS P30 CA023108NCI NIH HHS P30 CA023108-27NCI NIH HHS U54 CA151662NCRR NIH HHS NIGMS 1P30RR032136-01NCRR NIH HHS P30 RR032136NHLBI NIH HHS T32 HL105338NIAID NIH HHS 5T32AI007363-22NIAID NIH HHS T32 AI007363NIGMS NIH HHS P30 GM103415
6 · The paper itself

Abstract

Nanotechnology has tremendous potential to contribute to cancer immunotherapy. The 'in situ vaccination' immunotherapy strategy directly manipulates identified tumours to overcome local tumour-mediated immunosuppression and subsequently stimulates systemic antitumour immunity to treat metastases. We show that inhalation of self-assembling virus-like nanoparticles from cowpea mosaic virus (CPMV) reduces established B16F10 lung melanoma and simultaneously generates potent systemic antitumour immunity against poorly immunogenic B16F10 in the skin. Full efficacy required Il-12, Ifn-γ, adaptive immunity and neutrophils. Inhaled CPMV nanoparticles were rapidly taken up by and activated neutrophils in the tumour microenvironment as an important part of the antitumour immune response. CPMV also exhibited clear treatment efficacy and systemic antitumour immunity in ovarian, colon, and breast tumour models in multiple anatomic locations. CPMV nanoparticles are stable, nontoxic, modifiable with drugs and antigens, and their nanomanufacture is highly scalable. These properties, combined with their inherent immunogenicity and demonstrated efficacy against a poorly immunogenic tumour, make CPMV an attractive and novel immunotherapy against metastatic cancer.

Indexed as

AnimalsCancer VaccinesCell Line, TumorComovirusFemaleMiceMice, Inbred C57BLNanoparticlesNeoplasms, ExperimentalTreatment OutcomeVaccinationViral VaccinesCancer VaccinesViral Vaccines

Identifiers

PMID26689376
PMCPMC4777632

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.