Evidence map›Paper›PMID 40813770›Full record

ArticleNPJ vaccines2025

A self-amplifying mRNA vaccine expressing PRV gD induces robust immunity against virulent mutants.

Tong Ling, Zhang Xin, Li Huan-Huan, Zheng Ya-Ting, Liu Ya-Mei, Guo Rong-Li, Armando Mario Damiani, Chen Sai-Sai, Zhang Chuan-Jian, Duan Rui and 7 more

Abstract read
In one paragraph

Article in NPJ vaccines, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Garcinone C inhibits pseudorabies virus replication through EGF/PI3K/Akt axis.Frontiers in cellular and infection microbiology · 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

17 authors.

Tong Ling *Institute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Zhang Xin *Institute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Li Huan-HuanInstitute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Zheng Ya-TingInstitute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Liu Ya-MeiInstitute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Guo Rong-LiInstitute of Veterinary Medicine, Jiangsu Academy of Agricultural Science, Nanjing, 210014, China.
Armando Mario DamianiFaculty of Medical Sciences, National University of Cuyo, Mendoza, 5500, Argentina.
Chen Sai-SaiInstitute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Zhang Chuan-JianInstitute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Duan RuiJinfa Pharmaceutical (Nanjing) Co, Ltd, Nanjing, 210032, China.
Mao Shu-YuJinfa Pharmaceutical (Nanjing) Co, Ltd, Nanjing, 210032, China.
Yu Jia-LiJinfa Pharmaceutical (Nanjing) Co, Ltd, Nanjing, 210032, China.
Zhang Qian-QianJinfa Pharmaceutical (Nanjing) Co, Ltd, Nanjing, 210032, China.
Tao Ruo-NanJinfa Pharmaceutical (Nanjing) Co, Ltd, Nanjing, 210032, China.
Nikolaus OsterriederTierärztliche Hochschule Hannover, Bünteweg 2, 30559, Hannover, Germany. Klaus.Osterrieder@tiho-hannover.de.
Xia Shu-HuaJinfa Pharmaceutical (Nanjing) Co, Ltd, Nanjing, 210032, China. shuhua.xia@jinfapharma.com.
Wang Ji-ChunInstitute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China. 19970021@jaas.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudorabies virus (PRV) causes an acute febrile infectious disease of pigs. Since 2011, PRV variants have appeared and spread nationwide in China. mRNA vaccines present a safe alternative and can stimulate humoral and cellular immunity. We constructed a self-amplifying mRNA (saRNA) vaccine containing gD gene of a highly virulent PRV variant. In mice, the PRV saRNA gD vaccine induced high levels of neutralizing antibodies. In piglets, vaccination with the PRV saRNA gD vaccine at a dose of as little as 5 μg induced very strong humoral immunity and cellular immunity, providing full protection against challenge infection with very virulent PRV variants. Protection following vaccination with saRNA gD induced significantly stronger protection than attenuated live vaccines and inactivated vaccines. In addition, our results confirm that a PRV saRNA vaccine expressing only one antigen can induce excellent protection in weaned piglets. Hence, the PRV saRNA gD vaccine might be a very promising substitute for inactivated and live vaccines. Finally, we provide proof-of-concept for the development of self-amplifying mRNA vaccines for members of the Alphaherpesvirinae, including herpes simplex virus 1 and 2 as well as varicella zoster virus.

Identifiers

PMID40813770
PMCPMC12354905

What OpenQuestion holds

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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.