Evidence map›Paper›PMID 42801710›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Immune Checkpoint Inhibitor as a Fifth Component of Lipid Nanoparticles Enables Lymph Node-Targeting and Augments mRNA Vaccine Efficacy.

Minki Ha, Jaehyun Kim, Seyoung Kim, Gonna Somu Naidu, Sungchan Cho, Seok-Beom Yong

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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

6 authors.

Minki Ha *Laboratory of Practical Nanomedicine, Department of Medical and Biological Sciences, The Catholic University of Korea, Bucheon-si, Gyeonggi-do, Republic of Korea.ORCID https://orcid.org/0009-0006-3991-635X
Jaehyun Kim *Department of Bioengineering, Institute for Bioengineering and Biopharmaceutical Research, Hanyang University, Seoul, Republic of Korea.ORCID https://orcid.org/0009-0000-1428-0638
Seyoung KimNucleic Acid Therapeutics Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Chungcheongbuk-do, Republic of Korea.ORCID https://orcid.org/0009-0005-0438-4632
Gonna Somu NaiduCentre for Interdisciplinary Research, SRM University-AP, Amaravati, Andhra Pradesh, India.ORCID https://orcid.org/0000-0003-4822-0259
Sungchan ChoNucleic Acid Therapeutics Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Chungcheongbuk-do, Republic of Korea.ORCID https://orcid.org/0000-0001-7627-978X
Seok-Beom YongLaboratory of Practical Nanomedicine, Department of Medical and Biological Sciences, The Catholic University of Korea, Bucheon-si, Gyeonggi-do, Republic of Korea.ORCID https://orcid.org/0000-0003-1783-3802

Funding

National Research Council of Science & Technology GTL24023-000National Research Foundation of Korea RS-2025-24683233
6 · The paper itself

Abstract

mRNA-encapsulated lipid nanoparticles (LNPs) have been used to develop vaccines and therapeutics since the COVID-19 pandemic, and clinical studies have demonstrated therapeutic benefits of mRNA vaccines for various cancers. However, current LNP formulations still require functional modifications to tailor them for therapeutic and vaccine applications. Recently, fifth component-incorporated LNPs were developed to finely tune their functionality, including immunogenicity and organ-targeting ability. Here, biphenyl-structured amphiphilic PDL1 inhibitors are employed as a fifth component to modify LNPs. Amphiphilic PDL1 inhibitor-incorporated, ALC0315-based LNPs show higher lymph node targeting, with a 6.94-fold increase in mRNA expression in the inguinal lymph node, thereby improving lymph node expansion and immune cell infiltration and, consequently, inducing greater mRNA vaccine efficacy. Furthermore, a consistent lymph node-targeting effect of the fifth component-containing LNP was observed across studies using the SM102-based LNP formulation, suggesting its universality. In conclusion, this study demonstrates that PDL1 inhibitor-incorporated fifth-component LNP serves as a next-generation platform for mRNA vaccines.

Indexed as

drug deliverylipid nanoparticlemRNA vaccinePDL1 inhibitor‐incorporated LNP

Identifiers

PMID42801710
PMCPMC13616246

What OpenQuestion holds

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Registered trials

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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.