Evidence map›Paper›PMID 42804114›Full record

ReviewMolecular biomedicine2026

mRNA lipid nanoparticle vaccines: current status, challenges and future prospects.

Zhineng Wu, Jinghu Lou, Yi Cheng, Meng Li, Zengming Wang, Nan Liu, Xiang Gao, Aiping Zheng, Hui Zhang

Abstract readReview
In one paragraph

Review in Molecular biomedicine, 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

9 authors.

Zhineng WuAcademy of Military Medical Sciences, Beijing, 100850, China.
Jinghu LouAcademy of Military Medical Sciences, Beijing, 100850, China.
Yi ChengAcademy of Military Medical Sciences, Beijing, 100850, China.
Meng LiAcademy of Military Medical Sciences, Beijing, 100850, China.
Zengming WangAcademy of Military Medical Sciences, Beijing, 100850, China.
Nan LiuAcademy of Military Medical Sciences, Beijing, 100850, China.
Xiang GaoAcademy of Military Medical Sciences, Beijing, 100850, China. gaoxiang609@163.com.
Aiping ZhengAcademy of Military Medical Sciences, Beijing, 100850, China. apzheng@163.com.
Hui ZhangAcademy of Military Medical Sciences, Beijing, 100850, China. zhhui58@126.com.ORCID http://orcid.org/0000-0003-2535-5046

Funding

Innovative Research Group Project of the National Natural Science Foundation of China 82473861
6 · The paper itself

Abstract

mRNA vaccines have become a clinically validated vaccine platform, as demonstrated by the success of COVID-19 vaccines such as Comirnaty and Spikevax, owing to their rapid design, manufacturing scalability, and capacity to induce in situ antigen expression. A key factor underlying this success is the lipid nanoparticle (LNP) delivery system, which protects mRNA from degradation and promotes efficient cellular uptake and cytoplasmic delivery, thereby enabling the full potential of mRNA technology. The continued advancement of mRNA-LNP vaccines requires integrated optimization of mRNA design, LNP composition, and delivery strategies to achieve improved stability, efficient intracellular delivery, and balanced immune responses. Despite remarkable progress, challenges related to formulation stability, long-term storage stability, safety and reactogenicity concerns, and durability of immune protection continue to hinder the broader application of mRNA-LNP vaccine platforms. This review provides an integrated overview of recent advances in mRNA-LNP vaccines, covering mRNA molecular engineering, LNP composition and delivery mechanisms, immune responses, clinical progress, and current developmental challenges. Furthermore, emerging strategies, including thermostable formulations, next-generation LNPs with improved targeting capability, emerging RNA platforms, and artificial intelligence-assisted optimization of RNA sequences and lipid materials, are discussed. By summarizing current achievements and future opportunities, this review highlights key principles guiding the rational design of safer, more stable, and more precise mRNA-LNP vaccine platforms and provides insights into accelerating their clinical translation.

Indexed as

COVID-19COVID-19 VaccinesLipidsNanoparticlesRNA, MessengerAnimalsHumansLiposomesNanovaccinesSARS-CoV-2Vaccines, SyntheticCOVID-19 VaccinesLipid NanoparticlesLipidsLiposomesNanovaccinesRNA, MessengerVaccines, SyntheticAI-assisted designCancer immunotherapyInfectious diseasesLipid nanoparticlesMRNA vaccinesStabilityThermostable formulations

Identifiers

PMID42804114
PMCPMC13620059

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.