Evidence map›Paper›PMID 42774904›Full record

ArticleMolecular therapy. Nucleic acids2026

Novel lipid nanoparticle in a mRNA cancer vaccine drives tumor control via type I IFNs and effector CD8

Matthew J Gold, Douglas G Millar, Jun Liu, Haritha Menon, Yury Karpov, Kirstin Olsen, Liliam Teixeira Oliveira, Charlotte Dubé, Charles W Tran, Alisha R Elford and 5 more

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 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

15 authors.

Matthew J GoldProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.
Douglas G MillarTumor Immunotherapy Program, Princess Margaret Cancer Centre, 610 University Avenue, Toronto, ON M5G 2M9, Canada.
Jun LiuProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.
Haritha MenonProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.
Yury KarpovProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.
Kirstin OlsenProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.
Liliam Teixeira OliveiraProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.
Charlotte DubéProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.
Charles W TranDepartment of Immunology, University of Toronto, Toronto, ON, Canada.
Alisha R ElfordTumor Immunotherapy Program, Princess Margaret Cancer Centre, 610 University Avenue, Toronto, ON M5G 2M9, Canada.
Jordan A SchwartzProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.
Rajesh Krishnan Gopalakrishna PanickerProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.
Eric G MarcussonProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.
Pamela S OhashiTumor Immunotherapy Program, Princess Margaret Cancer Centre, 610 University Avenue, Toronto, ON M5G 2M9, Canada.
Natalia Martin OrozcoProvidence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB T2J 3J1, Canada.

Funding

cGMP Manufacture, Fill-Finish, Release, Analytical and Stability Testing and Stability Program of a Nanoparticle Based HIV Envelope Vaccine75N93022D00005 · NIAID · INTERNATIONAL AIDS VACCINE INITIATIVE · PI HASSELL, THOMAS · 2022 to 2025
$8.0M
Task Area A shall encompass annual follow-up of cohort members, clinical events investigations, study operations, and data analysis and manuscript writing. If implemented, Task A.1 will provide fundin75N92020D00005 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WATSON, KAROL E · 2020 to 2025
$5.1M
NHLBI NIH HHS 75N92020D00005NIAID NIH HHS 75N93022D00005NIDA NIH HHS 75N95020D00005NIH HHS 75N93023D00005NIH HHS 75N99020D00005
6 · The paper itself

Abstract

mRNA based vaccines utilizing lipid-based delivery systems have been used for cancer therapy with some success targeting tumor-associated antigens (TAAs) or neoantigens. However, in many patients, T cell exhaustion or tumor suppression impedes the induction of a protective anti-tumor T cell response, which suggests that additional activation signals are required to reduce antagonistic tumor effects and reinvigorate the T cells. Here we sought to evaluate novel ionizable lipids for lipid nanoparticle (LNP)-formulations containing a tumor antigen mRNA as a therapeutic treatment for solid tumors and identify key immunogenic features of successful ionizable lipid candidates. Focusing on the induction of a tissue-destructive immune response became the ideal

Indexed as

cancer immunotherapycellular immunitymRNA/LNPMT: clinical applicationstherapeutic cancer vaccinetype I IFN

Identifiers

PMID42774904
PMCPMC13594926

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.