Evidence map›Paper›PMID 41189730›Full record

ArticleAdvanced functional materials2024

Multifunctional Nanovaccine Sensitizes Breast Cancer to Immune Checkpoint Therapy.

Carina Peres, Ana I Matos, Bárbara Carreira, Liane I F Moura, Ron Kleiner, Daniella Vaskovich-Koubi, Keren Reshef, Shai Dulberg, Mafalda Verdial, João Conniot and 14 more

Abstract read
In one paragraph

Article in Advanced functional materials, 2024. 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
–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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Intranasal Multiepitope PD-L1-siRNA-Based Nanovaccine: The Next-Gen COVID-19 Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  8. Review
  9. Article
  10. Better, Faster, Stronger: Accelerating mRNA-Based Immunotherapies With Nanocarriers.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    Review
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

24 authors.

Carina PeresResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.
Ana I MatosResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.
Bárbara CarreiraResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.
Liane I F MouraResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.
Ron KleinerDepartment of Physiology and Pharmacology Faculty of Medicine Tel Aviv University Tel Aviv 6997801 Israel.
Daniella Vaskovich-KoubiDepartment of Physiology and Pharmacology Faculty of Medicine Tel Aviv University Tel Aviv 6997801 Israel.
Keren ReshefDepartment of Department of Pathology Faculty of Medicine Tel Aviv University Tel Aviv 6997801 Israel.
Shai DulbergDepartment of Department of Pathology Faculty of Medicine Tel Aviv University Tel Aviv 6997801 Israel.
Mafalda VerdialResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.
João ConniotResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.
Marta B AfonsoResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.
Rita C AcúrcioResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.
Afonso P BastoInstituto de Medicina Molecular João Lobo Antunes Faculdade de Medicina Universidade de Lisboa Av. Prof. Egas Moniz Lisbon 1649-028 Portugal.
Sofia MensuradoInstituto de Medicina Molecular João Lobo Antunes Faculdade de Medicina Universidade de Lisboa Av. Prof. Egas Moniz Lisbon 1649-028 Portugal.
Bruno Silva-SantosInstituto de Medicina Molecular João Lobo Antunes Faculdade de Medicina Universidade de Lisboa Av. Prof. Egas Moniz Lisbon 1649-028 Portugal.
Susana Constantino Rosa SantosCCUL@RISE Centro Cardiovascular da Universidade de Lisboa Faculdade de Medicina Universidade de Lisboa Av. Prof. Egas Moniz Lisbon 1649-028 Portugal.
Ana S VianaCentro de Química Estrutural Faculdade de Ciências Universidade de Lisboa Campo Grande Lisbon 1749-016 Portugal.
Liana C SilvaResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.
Cecília M P RodriguesResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.
Véronique PréatLouvain Drug Research Institute Advanced Drug Delivery & Biomaterials Université Catholique de Louvain Brussels 1200 Belgium.
Luís GraçaInstituto de Medicina Molecular João Lobo Antunes Faculdade de Medicina Universidade de Lisboa Av. Prof. Egas Moniz Lisbon 1649-028 Portugal.
Asaf MadiDepartment of Department of Pathology Faculty of Medicine Tel Aviv University Tel Aviv 6997801 Israel.
Ronit Satchi-FainaroDepartment of Physiology and Pharmacology Faculty of Medicine Tel Aviv University Tel Aviv 6997801 Israel.
Helena F FlorindoResearch Institute for Medicines (iMed.ULisboa) Faculdade de Farmácia Universidade de Lisboa Av. Prof. Gama Pinto Lisbon 1649-003 Portugal.ORCID https://orcid.org/0000-0002-4006-5840

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the primary cause of cancer-related death in women worldwide. Breast cancer subtypes are characterized by different gene expression patterns, which drive their prognostic factors and therapeutic options. Among them, triple-negative breast cancer (TNBC) is one of the deadliest due to its aggressiveness, high rate of early recurrence and distant metastases, and limited therapeutic options. Despite the recent approval of monoclonal antibodies targeting programmed cell death protein 1 (PD-1) or its ligand (PD-L1) for the treatment of TNBC patients with a locally recurrent unresectable or metastatic tumor expressing PD-L1, their response rate is very modest. It is reported that polymeric nanoparticle (NP)-based cancer vaccines, co-entrapping tumor-associated antigens, Toll-like receptor ligands and small interfering RNA (siRNA) targeting the expression of the immunosuppressive cytokine transforming growth factor (TGF)-β1 by dendritic cells, sensitized TNBC to the agonist immune checkpoint OX40, inhibiting tumor growth and increasing overall survival. This anti-tumor immune-mediated effect is also observed in a luminal type of mammary cancer similar to human disease. Therefore, these synergistic anticancer effects of αOX40 and the antigen-specific adaptive immunity induced by nanovaccine-mediated TGF-β silencing may guide the development of novel combination regimens able to improve the response rate to this aggressive tumor.

Indexed as

luminal B mammary cancernanotechnologyOX40 and PD‐1RNA and vaccine co‐deliverytriple‐negative breast cancer

Identifiers

PMID41189730
PMCPMC12581784

What OpenQuestion holds

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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.