Evidence map›Paper›PMID 39941106›Full record

ReviewInternational journal of molecular sciences2025

Enhancing CAR T-Cell Function with Domains of Innate Immunity Sensors.

Tjaša Mlakar, Mojca Skrbinek, Tina Fink, Duško Lainšček

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. 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. Review
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.

Tjaša MlakarDepartment of Synthetic Biology and Immunology, National Institute of Chemistry, 1000 Ljubljana, Slovenia.
Mojca SkrbinekDepartment of Synthetic Biology and Immunology, National Institute of Chemistry, 1000 Ljubljana, Slovenia.
Tina FinkDepartment of Synthetic Biology and Immunology, National Institute of Chemistry, 1000 Ljubljana, Slovenia.
Duško LainščekDepartment of Synthetic Biology and Immunology, National Institute of Chemistry, 1000 Ljubljana, Slovenia.ORCID 0000-0001-9613-5441

Funding

The Slovenian Research and Innovation Agency P4-0176, J4-4563, J7-4640
6 · The paper itself

Abstract

The innate immune system plays an important role in protecting the organism via recognizing the danger signals and pathogens through pattern recognition receptors. By sensing the danger signal and conveying the signaling towards the elimination of the threat, several families of these receptors, expressed on different myeloid and innate lymphoid cells, serve as the first defense line in the innate immunity. Toll-like receptors, C-type lectin receptors, and many other receptors therefore illustrate the importance of the protective role of the immune system. This was additionally confirmed by CAR T-cell-based cancer immunotherapy, where the patient's own immune system is being used for successful tumor elimination. CAR T-cells have proven themselves to be a potent therapeutic option, yet in some cases their efficiency could be enhanced. Innate immune sensors that include strong activation and signaling domains, for instance, part of the Toll-like receptors, MyD88 (Myeloid Differentiation Primary Response gene), NKG2D (Natural killer group 2-member D), and many other domains, could be used as a CAR building module to increase the functionality and potency of the CAR T-cells.

Indexed as

Immunity, InnateImmunotherapy, AdoptiveReceptors, Chimeric AntigenT-LymphocytesAnimalsHumansMyeloid Differentiation Factor 88NeoplasmsNK Cell Lectin-Like Receptor Subfamily KSignal TransductionToll-Like ReceptorsMyeloid Differentiation Factor 88NK Cell Lectin-Like Receptor Subfamily KReceptors, Chimeric AntigenToll-Like Receptorscancer immunotherapyCAR T-cellinnate immune systemToll-like receptor domains

Identifiers

PMID39941106
PMCPMC11818292

What OpenQuestion holds

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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.