Evidence map›Paper›PMID 24451168›Full record

ArticleBreast cancer research : BCR2014

Vaccines against human HER2 prevent mammary carcinoma in mice transgenic for human HER2.

Carla De Giovanni, Giordano Nicoletti, Elena Quaglino, Lorena Landuzzi, Arianna Palladini, Marianna Lucia Ianzano, Massimiliano Dall'Ora, Valentina Grosso, Dario Ranieri, Roberta Laranga and 7 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

29 citing papers in PubMed, 36 citations in OpenAlex.

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  11. Pre-conditioning modifies the TME to enhance solid tumor CAR T cell efficacy and endogenous protective immunity.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
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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

17 authors at 6 institutions in 2 countries.

Carla De Giovanni
Giordano Nicoletti
Elena Quaglino
Lorena Landuzzi
Arianna Palladini
Marianna Lucia Ianzano
Massimiliano Dall'Ora
Valentina Grosso
Dario Ranieri
Roberta Laranga
Stefania Croci
Augusto Amici
Manuel L Penichet
Manuela Iezzi
Federica Cavallo
Patrizia Nanni
Pier-Luigi Lollini
University of Bologna · ITIstituto Ortopedico Rizzoli · ITUniversity of Turin · ITUniversità di Camerino · ITUniversity of California, Los Angeles · USUniversity of Chieti-Pescara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe availability of mice transgenic for the human HER2 gene (huHER2) and prone to the development of HER2-driven mammary carcinogenesis (referred to as FVB-huHER2 mice) prompted us to study active immunopreventive strategies targeting the human HER2 molecule in a tolerant host.

methodsFVB-huHER2 mice were vaccinated with either IL-12-adjuvanted human HER2-positive cancer cells or DNA vaccine carrying chimeric human-rat HER2 sequences. Onset and number of mammary tumors were recorded to evaluate vaccine potency. Mice sera were collected and passively transferred to xenograft-bearing mice to assess their antitumor efficacy.

resultsBoth cell and DNA vaccines significantly delayed tumor onset, leading to about 65% tumor-free mice at 70 weeks, whereas mock-vaccinated FVB-huHER2 controls developed mammary tumors at a median age of 45 weeks. In the DNA vaccinated group, 65% of mice were still tumor-free at about 90 weeks of age. The number of mammary tumors per mouse was also significantly reduced in vaccinated mice. Vaccines broke the immunological tolerance to the huHER2 transgene, inducing both humoral and cytokine responses. The DNA vaccine mainly induced a high and sustained level of anti-huHER2 antibodies, the cell vaccine also elicited interferon (IFN)-γ production. Sera of DNA-vaccinated mice transferred to xenograft-carrying mice significantly inhibited the growth of human HER2-positive cancer cells.

conclusionsAnti-huHER2 antibodies elicited in the tolerant host exert antitumor activity.

Indexed as

Adoptive TransferAnimalsAntibodiesAntibody FormationCancer VaccinesCell Line, TumorErb-b2 Receptor Tyrosine KinasesFemaleHumansInterferon-gammaInterleukin-12Mammary Neoplasms, AnimalMCF-7 CellsMiceMice, TransgenicSpleenAntibodiesCancer VaccinesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesInterferon-gammaInterleukin-12Vaccines, DNA

Identifiers

PMID24451168
PMCPMC3979148
OpenAlexW2051762781

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LicenceCC BY
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Registered trials

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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.