Evidence map›Paper›PMID 41713095›Full record

ArticlePoultry science2026

A Self-amplifying mRNA vaccine for infectious laryngotracheitis virus (ILTV) induces efficient protective immunity.

Huan-Huan Li, Ling Tong, Sai-Sai Chen, Zhi-Xiang Bi, Gang Hu, Wan-Li Chen, Jia-Li Yu, Ruo-Nan Tao, Teng Huang, Shu-Hua Xia and 2 more

Abstract read
In one paragraph

Article in Poultry science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

12 authors.

Huan-Huan LiCollege of Animal Science and Technology, Guangxi University, Nanning 530004, China; Institute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China.
Ling TongInstitute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; National Research Center of Engineering and Technology for Veterinary Biology, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; Jiangsu Coinnovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, China; GuoTai (Taizhou) Center of Technology Innovation for Veterinary Biology, Taizhou 225300, China.
Sai-Sai ChenInstitute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; National Research Center of Engineering and Technology for Veterinary Biology, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; Jiangsu Coinnovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, China; GuoTai (Taizhou) Center of Technology Innovation for Veterinary Biology, Taizhou 225300, China.
Zhi-Xiang BiInstitute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; National Research Center of Engineering and Technology for Veterinary Biology, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; Jiangsu Coinnovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, China; GuoTai (Taizhou) Center of Technology Innovation for Veterinary Biology, Taizhou 225300, China.
Gang HuJinfa Pharmaceutical (Nanjing) Co., Ltd., Nanjing 210032, China.
Wan-Li ChenJinfa Pharmaceutical (Nanjing) Co., Ltd., Nanjing 210032, China.
Jia-Li YuJinfa Pharmaceutical (Nanjing) Co., Ltd., Nanjing 210032, China.
Ruo-Nan TaoJinfa Pharmaceutical (Nanjing) Co., Ltd., Nanjing 210032, China.
Teng HuangCollege of Animal Science and Technology, Guangxi University, Nanning 530004, China. Electronic address: thomashwang@gxu.edu.cn.
Shu-Hua XiaJinfa Pharmaceutical (Nanjing) Co., Ltd., Nanjing 210032, China. Electronic address: shuhua.xia@jinfapharma.com.
Nikolaus OsterriederTierärztliche Hochschule Hannover, Bünteweg 230559 Hannover, Germany. Electronic address: Klaus.Osterrieder@tiho-hannover.de.
Ji-Chun WangInstitute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; National Research Center of Engineering and Technology for Veterinary Biology, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China; Jiangsu Coinnovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, China; GuoTai (Taizhou) Center of Technology Innovation for Veterinary Biology, Taizhou 225300, China. Electronic address: 19970021@jaas.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infectious laryngotracheitis (ILT) continues to pose a significant threat to intensive poultry farming regions worldwide. Current control strategies primarily rely on live attenuated and recombinant live ILT virus (ILTV) vaccines. However, concerns persist regarding the potential reversion to virulence, recombination of vaccine viruses, and interference from maternal antibodies. mRNA vaccine platforms offer a novel and promising approach for developing next-generation ILTV vaccines. In this study, we designed a self-amplifying RNA (saRNA) vaccine incorporating the ILTV gD gene and evaluated its immunogenicity and protective efficacy in chickens. The saRNA-gD vaccine elicited robust humoral immunity, with serum neutralizing antibody titers reaching up to 1:415. All vaccinated chickens achieved seropositivity within 7 days post-vaccination (dpv). Significantly elevated levels of IL-2 cytokine were observed at 28 and 42 dpv compared to the LNP control group, suggesting the potential activation of cellular immune responses following vaccination. Animal challenge experiment revealed that the saRNA-gD vaccine effectively mitigated clinical symptoms induced by ILTV infection, conferring a protection rate of approximately 66.7%, which is comparable to that of the commercial recombinant fowl pox virus (rFPV-LT) vaccine. Quantification of viral loads in tracheal swabs and histopathological examination demonstrated that the saRNA-gD vaccine significantly reduced viral DNA copies in swabs and induced markedly milder histopathological changes. These findings indicate that the saRNA-gD vaccine induces potent immune responses and provides substantial protection against ILTV challenge, potentiating it as a highly promising vaccine candidate for the control of ILT in poultry.

Indexed as

ChickensHerpesviridae InfectionsHerpesvirus 1, GallidmRNA VaccinesPoultry DiseasesViral VaccinesAnimalsAntibodies, ViralVaccines, SyntheticAntibodies, ViralmRNA VaccinesVaccines, SyntheticViral VaccinesGlycoprotein DILTVImmune protectionsaRNA vaccineVirus-neutralizing antibody

Identifiers

PMID41713095
PMCPMC12926564

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.