Evidence map›Paper›PMID 37572354›Full record

ArticlePlant biotechnology journal2023

Rice-produced classical swine fever virus glycoprotein E2 with herringbone-dimer design to enhance immune responses.

Qianru Xu, Fanshu Ma, Daichang Yang, Qingmei Li, Liming Yan, Jiquan Ou, Longxian Zhang, Yunchao Liu, Quan Zhan, Rui Li and 11 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Plant biotechnology journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Correction.Plant biotechnology journal · 2024
    Article
  8. Article
  9. Review
  10. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 8 institutions in 1 country.

Qianru Xu *School of Basic Medical Sciences, Henan University, Kaifeng, China.ORCID 0000-0003-3982-5416
Fanshu Ma *International Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agriculture University, Zhengzhou, China.ORCID 0000-0002-5258-9158
Daichang YangCollege of Life Science, Wuhan University, Wuhan, China.
Qingmei LiKey Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou, China.
Liming YanLaboratory of Structural Biology, School of Medicine, Tsinghua University, Beijing, China.
Jiquan OuWuhan Healthgen Biotechnology Corp., Wuhan, China.
Longxian ZhangInternational Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agriculture University, Zhengzhou, China.
Yunchao LiuKey Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou, China.
Quan ZhanWuhan Healthgen Biotechnology Corp., Wuhan, China.
Rui LiKey Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou, China.
Qiang WeiKey Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou, China.
Hui HuInternational Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agriculture University, Zhengzhou, China.
Yanan WangKey Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou, China.
Xueyang LiInternational Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agriculture University, Zhengzhou, China.
Shenli ZhangInternational Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agriculture University, Zhengzhou, China.
Jifei YangKey Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou, China.
Shujun ChaiKey Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou, China.
Yongkun DuInternational Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agriculture University, Zhengzhou, China.
Li WangKey Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou, China.
Erqin ZhangInternational Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agriculture University, Zhengzhou, China.
Gaiping ZhangInternational Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agriculture University, Zhengzhou, China.
Henan Academy of Agricultural Sciences · CNHenan Agricultural University · CNWuhan Institute of Bioengineering · CNChinese Academy of Sciences · CNHenan University · CNPeking University · CNTsinghua University · CNWuhan University · CN

Funding

the Key Projects of Science and Technology of Henan Province 192102110007the Key Projects of Science and Technology of Henan Province 221100110600
6 · The paper itself

Abstract

Pestiviruses, including classical swine fever virus, remain a concern for global animal health and are responsible for major economic losses of livestock worldwide. Despite high levels of vaccination, currently available commercial vaccines are limited by safety concerns, moderate efficacy, and required high doses. The development of new vaccines is therefore essential. Vaccine efforts should focus on optimizing antigen presentation to enhance immune responses. Here, we describe a simple herringbone-dimer strategy for efficient vaccine design, using the classical swine fever virus E2 expressed in a rice endosperm as an example. The expression of rE2 protein was identified, with the rE2 antigen accumulating to 480 mg/kg. Immunological assays in mice, rabbits, and pigs showed high antigenicity of rE2. Two immunizations with 284 ng of the rE2 vaccine or one shot with 5.12 μg provided effective protection in pigs without interference from pre-existing antibodies. Crystal structure and small-angle X-ray scattering results confirmed the stable herringbone dimeric conformation, which had two fully exposed duplex receptor binding domains. Our results demonstrated that rice endosperm is a promising platform for precise vaccine design, and this strategy can be universally applied to other Flaviviridae virus vaccines.

Indexed as

Classical Swine FeverClassical Swine Fever VirusOryzaViral VaccinesAnimalsAntibodies, ViralImmunityMiceRabbitsSwineViral Envelope ProteinsAntibodies, ViralViral Envelope ProteinsViral VaccinesE2 proteinherringbone-dimerPestivirusrational vaccine designtransgenic rice

Identifiers

PMID37572354
PMCPMC10651154
OpenAlexW4385779510

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.