Evidence map›Paper›PMID 35672651›Full record

ArticleDrug delivery and translational research2022

Exploring chitosan-shelled nanobubbles to improve HER2 + immunotherapy via dendritic cell targeting.

Monica Argenziano, Sergio Occhipinti, Anna Scomparin, Costanza Angelini, Francesco Novelli, Marco Soster, Mirella Giovarelli, Roberta Cavalli

Open access · hybridAbstract read
In one paragraph

Article in Drug delivery and translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

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  7. Nanotechnology Applications in Breast Cancer Immunotherapy.Small (Weinheim an der Bergstrasse, Germany) · 2024
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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

8 authors at 1 institution in 1 country.

Monica Argenziano *Department of Drug Science and Technology, University of Turin, Via P. Giuria 9, 10125, Turin, Italy.
Sergio Occhipinti *Department of Molecular Biotechnology and Health Science, University of Turin, Via Nizza 52, 10126, Turin, Italy.
Anna ScomparinDepartment of Drug Science and Technology, University of Turin, Via P. Giuria 9, 10125, Turin, Italy.
Costanza AngeliniDepartment of Molecular Biotechnology and Health Science, University of Turin, Via Nizza 52, 10126, Turin, Italy.
Francesco NovelliDepartment of Molecular Biotechnology and Health Science, University of Turin, Via Nizza 52, 10126, Turin, Italy.
Marco SosterDepartment of Drug Science and Technology, University of Turin, Via P. Giuria 9, 10125, Turin, Italy.
Mirella GiovarelliDepartment of Molecular Biotechnology and Health Science, University of Turin, Via Nizza 52, 10126, Turin, Italy.
Roberta CavalliDepartment of Drug Science and Technology, University of Turin, Via P. Giuria 9, 10125, Turin, Italy. roberta.cavalli@unito.it.
University of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy is a valuable approach to cancer treatment as it is able to activate the immune system. However, the curative methods currently in clinical practice, including immune checkpoint inhibitors, present some limitations. Dendritic cell vaccination has been investigated as an immunotherapeutic strategy, and nanotechnology-based delivery systems have emerged as powerful tools for improving immunotherapy and vaccine development. A number of nanodelivery systems have therefore been proposed to promote cancer immunotherapy. This work aims to design a novel immunotherapy nanoplatform for the treatment of HER2 + breast cancer, and specially tailored chitosan-shelled nanobubbles (NBs) have been developed for the delivery of a DNA vaccine. The NBs have been functionalized with anti-CD1a antibodies to target dendritic cells (DCs). The NB formulations possess dimensions of approximately 300 nm and positive surface charge, and also show good physical stability up to 6 months under storage at 4 °C. In vitro characterization has confirmed that these NBs are capable of loading DNA with good encapsulation efficiency (82%). The antiCD1a-functionalized NBs are designed to target DCs, and demonstrated the ability to induce DC activation in both human and mouse cell models, and also elicited a specific immune response that was capable of slowing tumor growth in mice in vivo. These findings are the proof of concept that loading a tumor vaccine into DC-targeted chitosan nanobubbles may become an attractive nanotechnology approach for the future immunotherapeutic treatment of cancer.

Indexed as

Cancer VaccinesChitosanNeoplasmsAnimalsCell Line, TumorDendritic CellsImmunotherapyMiceCancer VaccinesChitosanCancer immunotherapyDendritic cellsDNA vaccineNanobubblesTargeted release

Identifiers

PMID35672651
PMCPMC9172608
OpenAlexW4281682031

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.