Evidence map›Paper›PMID 39436660›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

CXCL13 promotes broad immune responses induced by circular RNA vaccines.

Jiawu Wan, Caiqian Wang, Zongmei Wang, Lingli Wang, Haoran Wang, Ming Zhou, Zhen F Fu, Ling Zhao

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
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  9. From Bench to Bedside: Reframing theJournal of clinical & cellular immunology · 2026
    Article
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  11. Review
  12. Article
  13. Review
  14. Roles and Applications of Circular RNA in Virus Infection.International journal of molecular sciences · 2025
    Review
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  16. Review
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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.

Jiawu Wan *National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
Caiqian Wang *National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
Zongmei WangNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
Lingli WangNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
Haoran WangNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
Ming ZhouNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.
Zhen F FuNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.ORCID 0000-0001-6293-9329
Ling ZhaoNational Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China.ORCID 0000-0003-0569-8105

Funding

MOE | 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

Antibody responses induced by current vaccines for influenza and SARS-CoV-2 often lack robust cross-reactivity. As hubs where diverse immune cells converge and interact, the alterations in the immune microenvironment within lymph nodes (LNs) are intricately linked to immune responses. Herein, we designed a lipid nanoparticle (LNP) loaded with circular RNA (circRNA) and targeted to LNs, in which CXCL13 was directly integrated into antigen-encoding circRNA strands. We demonstrated that CXCL13 alters the transcriptomic profiles of LNs, especially the upregulation of IL-21 and IL-4. Meanwhile, CXCL13 promotes the formation of germinal center and elicits robust antigen-specific T cell responses. With the codelivery of CXCL13 and the antigen, CXCL13 enhances cross-reactive antibodies against influenza virus and SARS-CoV-2, achieving protection against both homologous and heterologous influenza virus challenges in a mouse model. Notably, the targeted modification of LNP surfaces with antibodies helps address some of the challenges associated with lyophilized LNP vaccines, which is crucial for the long-term storage of LNP-circRNA vaccines. Overall, the circRNA-based antigen-CXCL13 coexpression system developed herein provides a simple and robust platform that enhances the magnitude and breadth of antibody responses against multiple viral glycoproteins, highlighting the potential utility of CXCL13 in inducing broad immune responses.

Indexed as

Chemokine CXCL13COVID-19RNA, CircularSARS-CoV-2AnimalsAntibodies, ViralCOVID-19 VaccinesCross ReactionsFemaleHumansInfluenza VaccinesInterleukin-21Interleukin-4InterleukinsLymph NodesMiceAntibodies, ViralChemokine CXCL13COVID-19 VaccinesCxcl13 protein, mouseInfluenza VaccinesInterleukin-21Interleukin-4InterleukinsRNA, Circularbroadly cross-reactive antibodiescircRNA vaccineCXCL13influenza virusSARS-CoV-2

Identifiers

PMID39436660
PMCPMC11536096

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.