Evidence map›Paper›PMID 38052844›Full record

ArticleNature communications2023

A lung-selective delivery of mRNA encoding broadly neutralizing antibody against SARS-CoV-2 infection.

Wanbo Tai, Kai Yang, Yubin Liu, Ruofan Li, Shengyong Feng, Benjie Chai, Xinyu Zhuang, Shaolong Qi, Huicheng Shi, Zhida Liu and 11 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
9.3field-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

29 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  3. Anti-CD19-engineered exosomes enable B cell-targeted anti-BAFF mRNA delivery to alleviate lupus progression.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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  13. Review
  14. Nebulization of an mRNA-encoded monoclonal antibody for passive immunization of foals against Rhodococcus equi.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  15. Developing Biomaterial-Based mRNA Delivery System for Lung Disease Treatment.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Molecular therapy. Nucleic acids · 2025
    Article
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

21 authors at 8 institutions in 2 countries.

Wanbo Tai *New Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.ORCID 0000-0002-9864-8993
Kai Yang *Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, 100084, China.
Yubin Liu *New Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.ORCID 0000-0002-5531-6972
Ruofan Li *Beijing Advanced Innovation Center for Structural Biology, Beijing Frontier Research Center for Biological Structure, Center for Infectious Disease Research, School of Medicine, Tsinghua University, Beijing, 100084, China.
Shengyong Feng *New Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.
Benjie Chai *New Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.
Xinyu Zhuang *Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, 130122, China.
Shaolong QiKey Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, 100084, China.
Huicheng ShiNew Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.
Zhida LiuShanxi Academy of Advanced Research and Innovation, Taiyuan, 030032, China.
Jiaqi LeiKey Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, 100084, China.
Enhao MaNew Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.
Weixiao WangNew Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.
Chongyu TianNew Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.
Ting LeNew Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.
Jinyong WangInstitute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, 518132, China.
Yunfeng ChenInstitute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, 518132, China.ORCID 0000-0002-5185-4781
Mingyao TianChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, 130122, China. klwklw@126.com.ORCID 0000-0003-0360-3635
Ye XiangBeijing Advanced Innovation Center for Structural Biology, Beijing Frontier Research Center for Biological Structure, Center for Infectious Disease Research, School of Medicine, Tsinghua University, Beijing, 100084, China. yxiang@mail.tsinghua.edu.cn.ORCID 0000-0003-0230-9522
Guocan YuKey Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, 100084, China. guocanyu@mail.tsinghua.edu.cn.ORCID 0000-0003-1157-4184
Gong ChengNew Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China. gongcheng@mail.tsinghua.edu.cn.ORCID 0000-0001-7447-5488
Center for Life Sciences · CNShenzhen Bay Laboratory · CNTsinghua University · CNBeijing Advanced Sciences and Innovation Center · CNChangchun Institute of Optics, Fine Mechanics and Physics · CNChinese Academy of Agricultural Sciences · CNKing Center · USShanxi Academy of Building Research · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 31700148National Natural Science Foundation of China (National Science Foundation of China) 31825001National Natural Science Foundation of China (National Science Foundation of China) 32100755National Natural Science Foundation of China (National Science Foundation of China) 32188101National Natural Science Foundation of China (National Science Foundation of China) 81730063National Natural Science Foundation of China (National Science Foundation of China) 8191101056National Natural Science Foundation of China (National Science Foundation of China) 81961160737National Natural Science Foundation of China (National Science Foundation of China) 82041006National Natural Science Foundation of China (National Science Foundation of China) 82271872
6 · The paper itself

Abstract

The respiratory system, especially the lung, is the key site of pathological injury induced by SARS-CoV-2 infection. Given the low feasibility of targeted delivery of antibodies into the lungs by intravenous administration and the short half-life period of antibodies in the lungs by intranasal or aerosolized immunization, mRNA encoding broadly neutralizing antibodies with lung-targeting capability can perfectly provide high-titer antibodies in lungs to prevent the SARS-CoV-2 infection. Here, we firstly identify a human monoclonal antibody, 8-9D, with broad neutralizing potency against SARS-CoV-2 variants. The neutralization mechanism of this antibody is explained by the structural characteristics of 8-9D Fabs in complex with the Omicron BA.5 spike. In addition, we evaluate the efficacy of 8-9D using a safe and robust mRNA delivery platform and compare the performance of 8-9D when its mRNA is and is not selectively delivered to the lungs. The lung-selective delivery of the 8-9D mRNA enables the expression of neutralizing antibodies in the lungs which blocks the invasion of the virus, thus effectively protecting female K18-hACE2 transgenic mice from challenge with the Beta or Omicron BA.1 variant. Our work underscores the potential application of lung-selective mRNA antibodies in the prevention and treatment of infections caused by circulating SARS-CoV-2 variants.

Indexed as

COVID-19SARS-CoV-2AnimalsAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesFemaleHumansLungMiceMice, TransgenicRNA, MessengerSpike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesRNA, MessengerSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID38052844
PMCPMC10697968
OpenAlexW4389348499

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.