Evidence map›Paper›PMID 42497177›Full record

ArticlePLoS pathogens2026

Broad and durable protection against SARS-CoV-2 and SARS-CoV by an intranasal chimpanzee adenovirus vaccine expressing tandem RBDs and nucleocapsid.

Yaping Liu, Runhong Zhou, Tian Zhao, Ruoke Wang, Kun Zhu, Junxian Hong, Ziqing Yang, Qianqian Yang, Yuqing Lei, Yang Bai and 8 more

Abstract read
In one paragraph

Article in PLoS pathogens, 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

18 authors.

Yaping LiuComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Runhong ZhouAIDS Institute, Department of Microbiology and Pandemic Research Alliance Unit, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, People's Republic of China.
Tian ZhaoSchool of Biomedical Engineering, Tsinghua University, Beijing, China.
Ruoke WangComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Kun ZhuComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Junxian HongComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Ziqing YangComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Qianqian YangComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Yuqing LeiComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Yang BaiSchool of Basic Medical Sciences, Tsinghua University, Beijing, China.
Jing WeiComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Peng ChenComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Xinyu FanComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Qi ZhangComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Xuanling ShiComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Peng LiuSchool of Biomedical Engineering, Tsinghua University, Beijing, China.
Zhiwei ChenAIDS Institute, Department of Microbiology and Pandemic Research Alliance Unit, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, People's Republic of China.
Linqi ZhangComprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.ORCID 0000-0003-4931-509X

Funding

Wellcome Trust
6 · The paper itself

Abstract

Current intramuscular COVID-19 vaccines reduce severe disease but offer limited protection against infection, enabling viral persistence, immune escape, and transmission. We developed intranasal rare-serotype chimpanzee adenovirus 68 (AdC68)-based vaccines expressing heterologous tandem receptor-binding domains from SARS-CoV-2, SARS-CoV, and MERS-CoV, fused to the SARS-CoV-2 nucleocapsid (AdC68-4RBD(XBB.1.5)-N) to enhance both B and T cell responses. Antigen integrity was confirmed by receptor binding and recognition by multiple conformation-sensitive monoclonal antibodies. In mice, intranasal AdC68-4RBD(XBB.1.5)-N elicited potent and durable mucosal and systemic immunity, including serum/saliva IgA and broad neutralizing antibodies persisting up to 40 weeks, alongside tissue-localized B and T cells. Monoclonal antibodies from long-lived bone marrow antibody-secreting cells demonstrated broad and strain-specific neutralization, providing mechanistic insight into the breadth and longevity of the antibody response. In Syrian hamsters, intranasal immunization protected against SARS-CoV-2 XBB.1.5 replication in nasal turbinates and lungs and blocked transmission for up to four months post-vaccination. Robust protection against SARS-CoV challenge was demonstrated in K18-hACE2 transgenic mice, further confirming its broad efficacy. These findings support AdC68-4RBD(XBB.1.5)-N as a promising mucosal vaccine candidate to prevent infection and transmission of pathogenic coronaviruses.

Indexed as

Adenoviruses, SimianCOVID-19COVID-19 VaccinesSARS-CoV-2Severe acute respiratory syndrome-related coronavirusAdministration, IntranasalAnimalsAntibodies, NeutralizingAntibodies, ViralCoronavirus Nucleocapsid ProteinsFemaleHumansMicePan troglodytesSpike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralCoronavirus Nucleocapsid ProteinsCOVID-19 VaccinesSpike Glycoprotein, Coronavirus

Identifiers

PMID42497177
PMCPMC13399337

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.