Evidence map›Paper›PMID 42514660›Full record

ArticleVeterinary sciences2026

Occurrence of Antibody-Dependent Enhancement of Avian Infectious Bronchitis in Target Animal Experiments.

Lin Cheng, Di Wang, Jia-Rui Zhang, Yi-Han Zhang, Xin-Rui Wu, Ya-Mei Huang, Min Li, Fu-Yan Wang, Yang Zhao, Xin-Feng Han and 3 more

Abstract read
In one paragraph

Article in Veterinary sciences, 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

13 authors.

Lin ChengCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Di WangCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Jia-Rui ZhangCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Yi-Han ZhangCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Xin-Rui WuCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Ya-Mei HuangCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Min LiAnimal Disease Prevention and Control Center of Chengdu City, Chengdu 610000, China.
Fu-Yan WangCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Yang ZhaoCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Xin-Feng HanCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Min CuiCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Yong HuangCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.ORCID 0000-0001-8897-5651
Jing XiaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.ORCID 0000-0002-3503-8936

Funding

National Natural Science Foundation of China 32302906Natural Science Foundation of Sichuan Province 2024NSFSC1280Regional innovation cooperation Program of the Science and Technology Department of Sichuan Province 2024YFHZ0111Sichuan Province innovation team project SCCXTD-2026-24
6 · The paper itself

Abstract

Outbreaks of avian infectious bronchitis virus (IBV) often occur in vaccinated flocks. The antibody-dependent enhancement (ADE) has been proposed as a potential mechanism underlying coronavirus vaccine failure. However, this hypothesis has yet to be substantiated in flocks. This study demonstrates ADE occurrence in IBV (gamacoronavirus) in vitro and in vivo. Using the SPF chicken host model, primary infection with an O-glycosylation-modified attenuated strain enhanced pathogenesis upon secondary homologous/heterologous virulent challenge, increasing morbidity/mortality (≥30%), pathological lesions, and viral loads. Notably, sequentially attenuated infections also induced ADE, suggesting live attenuated vaccine risks. The immune serum raised against the O-glycosylation-modified attenuated strain was also pre-mixed with the challenge strain, and the mixtures were then inoculated into target cells, non-susceptible macrophage cells, or a co-culture of both cell types. The serum-virus complexes replicated poorly in macrophages, yet immune cells amplified the expression of inflammatory factors and ADE-mediated viral replication in target cells, indicating a significant promoting role of immune cells in this process. The concentrations of complement component C3 and neutralizing antibodies in the immune serum were also measured, and results showed that the induction of this ADE is associated with high complement component C3 and low neutralizing antibody titers. These findings highlight risks for vaccines and antibody-based therapeutic strategies of coronavirus infection.

Indexed as

ADEantibody dependent enhancementcomplementcoronavirusIBVinfectious bronchitis virus

Identifiers

PMID42514660
PMCPMC13417425

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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.