ArticleACS nano2025
Customizable mRNA Lipid Nanoparticles for Transfection of Primary Human T Cells.
Article in ACS nano, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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.
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.
Who cites it
5 citing papers in PubMed.
- Human T cell engineering via serial delivery of mRNA encapsulated within lipid nanoparticles.Molecular therapy. Nucleic acids · 2026Article
- Optimizing C14120-based lipid nanoparticles for mRNA delivery: Editorial commentary.Molecular therapy. Nucleic acids · 2026Article
- In Vivo mRNA-Lipid Nanoparticle CAR-T Cell Engineering: Advances, Challenges, and Clinical Translation.Biomedicines · 2026Review
- AZD5582 robustly reactivates latently infected cells and clears the majority of those reactivated from the SIV reservoir.bioRxiv : the preprint server for biology · 2026Article
- The Nanoparticle Delivery Gap in Immune Cell Engineering: From Uptake to Endosomal Escape.International journal of nanomedicine · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
A central goal of genetic therapies, including RNA-based medicines, is to develop vectors that enable clinical translation for the treatment of specific cell types. T cells provide a unique opportunity for genetic medicines, particularly in their relevance to CAR-T cell therapies, autoimmune diseases, and vaccines. However, T cells are notoriously difficult to transfect, and many RNA delivery vectors are designed with model systems that may not reflect true T cell morphology, compounding the difficulty in isolating trends in particle properties that promote efficacy. Here, we use primary human T cell populations and leverage design of experiment to optimize a lipid nanoparticle (LNP)-based delivery vector for genetic therapies in T cells. In doing so, we discern key trends in LNP composition that promote better efficacy in both the uptake and expression of mRNA, namely, that high cholesterol and low polyethylene glycol (PEG) compositions aid in the efficacy of the LNPs. Informed by these trends, our novel
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What Socratic holds
Registered trials
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 Socratic graph.