Evidence map›Paper›PMID 37901327›Full record

ArticleFrontiers in oncology2023

Targeting of tumor cells by custom antigen transfer: a novel approach for immunotherapy of cancer.

Ilaria Nesi, Chiara Della Bella, Maria Letizia Taddei, Alice Santi, Erica Pranzini, Paolo Paoli, Mario Milco D'Elios, Matteo Ramazzotti, Massimo Genovese, Anna Caselli and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 70% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

Ilaria NesiDepartment of Experimental and Clinical Biomedical Sciences, University of Firenze, Firenze, Italy.
Chiara Della BellaDepartment of Experimental and Clinical Medicine, University of Firenze, Firenze, Italy.
Maria Letizia TaddeiDepartment of Experimental and Clinical Medicine, University of Firenze, Firenze, Italy.
Alice SantiDepartment of Experimental and Clinical Biomedical Sciences, University of Firenze, Firenze, Italy.
Erica PranziniDepartment of Experimental and Clinical Biomedical Sciences, University of Firenze, Firenze, Italy.
Paolo PaoliDepartment of Experimental and Clinical Biomedical Sciences, University of Firenze, Firenze, Italy.
Mario Milco D'EliosDepartment of Molecular and Developmental Medicine, University of Siena, Siena, Italy.
Matteo RamazzottiDepartment of Experimental and Clinical Biomedical Sciences, University of Firenze, Firenze, Italy.
Massimo GenoveseDepartment of Experimental and Clinical Biomedical Sciences, University of Firenze, Firenze, Italy.
Anna CaselliDepartment of Experimental and Clinical Biomedical Sciences, University of Firenze, Firenze, Italy.
Paolo CirriDepartment of Experimental and Clinical Biomedical Sciences, University of Firenze, Firenze, Italy.
University of Florence · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the early stages of carcinogenesis, the transformed cells become "invisible" to the immune system. From this moment on, the evolution of the tumor depends essentially on the genotype of the primitive cancer cells and their subsequent genetic drift. The role of the immune system in blocking tumor progression from the earliest stages is largely underestimated because by the time tumors are clinically detectable, the immune system has already completely failed its task. Therefore, a clinical treatment capable of restoring the natural anti-tumor role of the immune system could prove to be the "ultimate weapon" against cancer. Herein, we propose a novel therapeutic approach for the treatment of solid cancer that exploits the capability of activated monocytes to transfer major histocompatibility complex I (MHC-I) molecules bound to antigenic peptides to cancer cells using microvesicles as cargo, making tumor cells target of a "natural" CD8

Indexed as

cancer therapyectosomesextracellular vesiclesimmunotargetingimmunotherapymicrovesiclestumor microenvironment

Identifiers

PMID37901327
PMCPMC10612144
OpenAlexW4387609727

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.