Evidence map›Paper›PMID 38631709›Full record

ArticleJournal for immunotherapy of cancer2024

Preclinical evaluation of two phylogenetically distant arenavirus vectors for the development of novel immunotherapeutic combination strategies for cancer treatment.

Josipa Raguz, Catarina Pinto, Theresa Pölzlbauer, Mohamed Habbeddine, Sandra Rosskopf, Judith Strauß, Valentin Just, Sarah Schmidt, Katell Bidet Huang, Felix Stemeseder and 6 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 5 citations in OpenAlex.

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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

16 authors at 2 institutions in 2 countries.

Josipa RaguzHookipa Pharma Inc, New York, NY, USA.ORCID 0000-0002-6416-0586
Catarina PintoHookipa Pharma Inc, New York, NY, USA.ORCID 0000-0002-9021-7005
Theresa PölzlbauerHookipa Pharma Inc, New York, NY, USA.
Mohamed HabbeddineHookipa Pharma Inc, New York, NY, USA.
Sandra RosskopfHookipa Pharma Inc, New York, NY, USA.
Judith StraußHookipa Pharma Inc, New York, NY, USA.
Valentin JustHookipa Pharma Inc, New York, NY, USA.
Sarah SchmidtHookipa Pharma Inc, New York, NY, USA.
Katell Bidet HuangHookipa Pharma Inc, New York, NY, USA.
Felix StemesederHookipa Pharma Inc, New York, NY, USA.
Timo SchippersHookipa Pharma Inc, New York, NY, USA.
Ethan StewartVienna BioCenter Core Facilities GmbH (VBCF), Vienna, Austria.
Jakub JezVienna BioCenter Core Facilities GmbH (VBCF), Vienna, Austria.
Pedro BerraondoProgram of Immunology and Immunotherapy, Cima Universidad de Navarra, Pamplona, Spain.ORCID 0000-0001-7410-1865
Klaus K OrlingerHookipa Pharma Inc, New York, NY, USA.
Henning LauterbachHookipa Pharma Inc, New York, NY, USA Henning.Lauterbach@hookipapharma.com.ORCID 0000-0002-6062-5163
Vienna Biocenter · ATNavarre Institute of Health Research · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEngineered arenavirus vectors have recently been developed to leverage the body's immune system in the fight against chronic viral infections and cancer. Vectors based on Pichinde virus (artPICV) and lymphocytic choriomeningitis virus (artLCMV) encoding a non-oncogenic fusion protein of human papillomavirus (HPV)16 E6 and E7 are currently being tested in patients with HPV16+ cancer, showing a favorable safety and tolerability profile and unprecedented expansion of tumor-specific CD8

methodsTo advance our understanding of the immunobiology of these two vectors, we analyzed and compared their individual properties in preclinical in vivo and in vitro systems. Immunogenicity and antitumor effect of intratumoral or intravenous administration of both vectors, as well as combination with NKG2A blockade, were evaluated in naïve or TC-1 mouse tumor models. Flow cytometry, Nanostring, and histology analysis were performed to characterize the tumor microenvironment (TME) and T-cell infiltrate following treatment.

resultsDespite being phylogenetically distant, both vectors shared many properties, including preferential infection and activation of professional antigen-presenting cells, and induction of potent tumor-specific CD8

conclusionsThe artARENA platform represents a strong therapeutic vaccine approach for the treatment of cancer. The induced antitumor immune response builds the backbone for novel combination therapies, which warrant further investigation.

Indexed as

ArenavirusNeoplasmsPapillomavirus InfectionsPapillomavirus VaccinesAnimalsCD8-Positive T-LymphocytesDisease Models, AnimalHumansImmunosuppression TherapyMicePapillomavirus E7 ProteinsTumor MicroenvironmentPapillomavirus E7 ProteinsPapillomavirus VaccinesDrug Therapy, CombinationHead and Neck CancerImmunogenicity, VaccineImmunotherapyTumor Microenvironment

Identifiers

PMID38631709
PMCPMC11029282
OpenAlexW4394893976

What OpenQuestion holds

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LicenceCC BY-NC
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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.