Evidence map›Paper›PMID 41809368›Full record

ArticleMolecular therapy. Oncology2026

Intravenous oncolytic vaccinia expressing transgenes for enhanced safety, inhibition of shedding, imaging, and systemic cancer immunotherapy.

Liliana Maruri-Avidal, Prajit Limsirichai, Nathaniel Gulizia, David H Kirn

Abstract read
In one paragraph

Article in Molecular therapy. Oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Liliana Maruri-AvidalReIGNITE Therapeutics, Inc, San Diego, CA 92121, USA.
Prajit LimsirichaiIGNITE Immunotherapy, Inc., Alameda, CA, USA.
Nathaniel GuliziaIGNITE Immunotherapy, Inc., Alameda, CA, USA.
David H KirnReIGNITE Therapeutics, Inc, San Diego, CA 92121, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncolytic viruses are broad-spectrum cancer immunotherapies with multiple mechanisms of action that complement other therapeutics, but concerns remain regarding intravenous (i.v.) safety, overexpression of transgenes, environmental shedding, and lack of imaging in patients. Here we describe the engineering and evaluation of an i.v. oncolytic vaccinia virus (VV) therapeutic expressing a hyperactive and selective herpes simplex virus thymidine kinase (HSV-TK.007). In the presence of i.v. or topical ganciclovir (GCV), HSV-TK.007 acted to block VV replication either systemically or topically for control of skin lesions and shedding, respectively. HSV-TK.007 expression also enabled systemic positron emission tomography-computed tomography (PET-CT) imaging of tumor-specific virus replication

Indexed as

cancer immunotherapygenetic medicineintravenous immunotherapyMT: Regular Issuenon-invasive imagingoncolytic vaccinia virussafety switchviral therapy

Identifiers

PMID41809368
PMCPMC12969024

What OpenQuestion holds

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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.