Evidence map›Paper›PMID 38078742›Full record

ArticlemBio2024

Circular RNA vaccines with long-term lymph node-targeting delivery stability after lyophilization induce potent and persistent immune responses.

Jiawu Wan, Zongmei Wang, Lingli Wang, Liqin Wu, Chengguang Zhang, Ming Zhou, Zhen F Fu, Ling Zhao

Open access · goldAbstract read
In one paragraph

Article in mBio, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
9.8field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 64 citations in OpenAlex.

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  19. Roles and Applications of Circular RNA in Virus Infection.International journal of molecular sciences · 2025
    Review
  20. Advances and Strategies in Enhancing mRNA Cancer Vaccines.Advanced materials (Deerfield Beach, Fla.) · 2025
    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

8 authors at 1 institution in 1 country.

Jiawu Wan *National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.ORCID 0000-0002-4728-0519
Zongmei Wang *National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Lingli WangNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Liqin WuNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Chengguang ZhangNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Ming ZhouNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Zhen F FuNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Ling ZhaoNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.ORCID 0000-0003-0569-8105
Huazhong Agricultural University · CN

Funding

DEGP | Major Projects of Guangdong Education Department for Foundation Research and Applied Research 2020B0301030007MOE | Fundamental Research Funds for the Central Universities (Fundamental Research Fund for the Central Universities) 2662023PY005MOST | National Key Research and Development Program of China (NKPs) 2022YFD1800100
6 · The paper itself

Abstract

importancemessenger RNA (mRNA) vaccines are a key technology in combating existing and emerging infectious diseases. However, the inherent instability of mRNA and the nonspecificity of lipid nanoparticle-encapsulated (LNP) delivery systems result in the need for cold storage and a relatively short-duration immune response to mRNA vaccines. Herein, we develop a novel vaccine in the form of circRNAs encapsulated in LNPs, and the circular structure of the circRNAs enhances their stability. Lyophilization is considered the most effective method for the long-term preservation of RNA vaccines. However, this process may result in irreversible damage to the nanoparticles, particularly the potential disruption of targeting modifications on LNPs. During the selection of lymph node-targeting ligands, we found that LNPs modified with mannose maintained their physical properties almost unchanged after lyophilization. Additionally, the targeting specificity and immunogenicity remained unaffected. In contrast, even with the addition of cryoprotectants such as sucrose, the physical properties of LNPs were impaired, leading to an obvious decrease in immunogenicity. This may be attributed to the protective role of mannose on the surface of LNPs during lyophilization. Freshly prepared and lyophilized mLNP-circRNA vaccines elicited comparable immune responses in both the rabies virus model and the SARS-CoV-2 model. Our data demonstrated that mLNP-circRNA vaccines elicit robust immune responses while improving stability after lyophilization, with no compromise in tissue targeting specificity. Therefore, mannose-modified LNP-circRNA vaccines represent a promising vaccine design strategy.

Indexed as

RNA, CircularVaccinesFreeze DryingImmunityMannoseRNA, MessengerMannoseRNA, CircularRNA, MessengerVaccinesCircRNA vaccinehumoral immunitylong-term protectionlymph node-targeting deliverylyophilization

Identifiers

PMID38078742
PMCPMC10790773
OpenAlexW4389558967

What OpenQuestion holds

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LicenceCC BY
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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.