Evidence map›Paper›PMID 42170676›Full record

ReviewMolecular therapy. Oncology2026

Engineering precision oncology: Targeting tumors and immune cells with lentiviral vectors.

Julia Rossi, Chiara Martinello, Riccardo Sorrentino, Véronique Guyonnet-Duperat, Samuel Amintas, Maria Jimena Abrey Recalde, Els Verhoeyen, Sandrine Dabernat

Abstract readReview
In one paragraph

Review in Molecular therapy. Oncology, 2026. 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
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.

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

8 authors.

Julia RossiUniversity Bordeaux, INSERM, BRIC, 1312 Bordeaux, France.
Chiara MartinelloCIRI - International Center for Infectiology Research, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, Ecole Normale Supérieure de Lyon, Université Lyon, 69007 Lyon, France.
Riccardo SorrentinoUniversity Bordeaux, INSERM, BRIC, 1312 Bordeaux, France.
Véronique Guyonnet-DuperatPlateforme VECT'UB, INSERM US 005 - CNRS UMS 3427- TBM-Core, Université de Bordeaux, 33000 Bordeaux, France.
Samuel AmintasUniversity Bordeaux, INSERM, BRIC, 1312 Bordeaux, France.
Maria Jimena Abrey RecaldeUniversity Bordeaux, INSERM, BRIC, 1312 Bordeaux, France.
Els VerhoeyenCIRI - International Center for Infectiology Research, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, Ecole Normale Supérieure de Lyon, Université Lyon, 69007 Lyon, France.
Sandrine DabernatUniversity Bordeaux, INSERM, BRIC, 1312 Bordeaux, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lentiviral vectors (LVs) are emerging as versatile tools for the efficient and stable delivery of therapeutic genes. Although VSV-G-pseudotyped LVs remain the standard for

Indexed as

cancer therapyimmunityin vivo gene therapylentiviral vectorLV pseudotypingMT: Regular IssueparamyxovirusSindbis virustumor targetingVSV-G

Identifiers

PMID42170676
PMCPMC13188084

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.