Evidence map›Paper›PMID 42506598›Full record

ArticleVaccines2026

A Repeated and Delayed Homologous Challenge Study Evaluating the Durability of Protection Induced by the Live Attenuated ASF Vaccine Candidate ASFV-G-ΔI177L/ΔLVR.

Xinghua Zheng, Yeonji Kim, Sun A Choi, Su Jin Lee, Seung Pyo Shin, Se Young Lee, Wonjun Kim, Seong Cheol Moon, Yongwoo Shin, Do Soon Kim and 6 more

Abstract read
In one paragraph

Article in Vaccines, 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

16 authors.

Xinghua ZhengCentral Research & Development Institute, Komipharm International Co., Ltd., Siheung-si 15094, Republic of Korea.
Yeonji KimWildlife Disease Response Team, National Institute of Wildlife Disease Control and Prevention (NIWDC), Ministry of Climate, Energy and Environment (MCEE), Songamgil 1, Gwangsan-gu, Gwangju 62407, Republic of Korea.ORCID 0009-0008-4078-8310
Sun A ChoiCentral Research & Development Institute, Komipharm International Co., Ltd., Siheung-si 15094, Republic of Korea.ORCID 0009-0004-7770-5022
Su Jin LeeCentral Research & Development Institute, Komipharm International Co., Ltd., Siheung-si 15094, Republic of Korea.
Seung Pyo ShinCentral Research & Development Institute, Komipharm International Co., Ltd., Siheung-si 15094, Republic of Korea.
Se Young LeeCentral Research & Development Institute, Komipharm International Co., Ltd., Siheung-si 15094, Republic of Korea.
Wonjun KimWildlife Disease Response Team, National Institute of Wildlife Disease Control and Prevention (NIWDC), Ministry of Climate, Energy and Environment (MCEE), Songamgil 1, Gwangsan-gu, Gwangju 62407, Republic of Korea.
Seong Cheol MoonCentral Research & Development Institute, Komipharm International Co., Ltd., Siheung-si 15094, Republic of Korea.
Yongwoo ShinWildlife Disease Response Team, National Institute of Wildlife Disease Control and Prevention (NIWDC), Ministry of Climate, Energy and Environment (MCEE), Songamgil 1, Gwangsan-gu, Gwangju 62407, Republic of Korea.
Do Soon KimCentral Research & Development Institute, Komipharm International Co., Ltd., Siheung-si 15094, Republic of Korea.
Byung-Chul ShinWildlife Disease Response Team, National Institute of Wildlife Disease Control and Prevention (NIWDC), Ministry of Climate, Energy and Environment (MCEE), Songamgil 1, Gwangsan-gu, Gwangju 62407, Republic of Korea.
Sua ChoiWildlife Disease Response Team, National Institute of Wildlife Disease Control and Prevention (NIWDC), Ministry of Climate, Energy and Environment (MCEE), Songamgil 1, Gwangsan-gu, Gwangju 62407, Republic of Korea.
Ji-Yun SungWildlife Disease Response Team, National Institute of Wildlife Disease Control and Prevention (NIWDC), Ministry of Climate, Energy and Environment (MCEE), Songamgil 1, Gwangsan-gu, Gwangju 62407, Republic of Korea.
Garam KimWildlife Disease Response Team, National Institute of Wildlife Disease Control and Prevention (NIWDC), Ministry of Climate, Energy and Environment (MCEE), Songamgil 1, Gwangsan-gu, Gwangju 62407, Republic of Korea.
Weonhwa JheongWildlife Disease Response Team, National Institute of Wildlife Disease Control and Prevention (NIWDC), Ministry of Climate, Energy and Environment (MCEE), Songamgil 1, Gwangsan-gu, Gwangju 62407, Republic of Korea.
Jung Hyang SurCentral Research & Development Institute, Komipharm International Co., Ltd., Siheung-si 15094, Republic of Korea.ORCID 0009-0008-9734-5852

Funding

Ministry of Environment NIWDC-2025-RP-06the National Institute of Wildlife Disease Control and Prevention (NIWDC), Ministry of Climate, Energy and Environment (MCEE) of the Republic of Korea NIWDC-2025-RP-06
6 · The paper itself

Abstract

BACKGROUND/

objectivesAfrican swine fever (ASF) is a highly lethal disease of domestic pigs and wild suids that continues to cause substantial economic losses worldwide. Despite recent progress in live attenuated ASF vaccine development, evidence supporting durable protection under repeated exposure conditions representative of endemic settings remains limited. Here, we assessed the long-term safety and protective efficacy of a live attenuated ASFV-G-ΔI177L/ΔLVR vaccine using a repeated-challenge experimental design intended to model re-exposure in ASF-endemic regions.

methodsVaccinated pigs were subjected to homologous virulent ASF virus challenges at multiple intervals, including repeated challenges (three sequential inoculations) and single challenges administered at 8 and 12 weeks post-vaccination.

resultsAcross all challenge regimens, vaccinated animals survived and remained clinically healthy, including those receiving three challenges, supporting sustained protection under repeated exposure pressure. Animals challenged at 8 or 12 weeks post-vaccination likewise exhibited complete survival, indicating maintained efficacy through at least 12 weeks. No vaccine-associated adverse clinical outcomes were detected over the study period, and post-challenge viral shedding was minimal.

conclusionsOverall, these data demonstrate that the candidate live attenuated ASF vaccine provides excellent protective efficacy and confers sustained protection against homologous ASF virus infection. This result is expected to be equally applicable under repeated exposure conditions in regions with unstable ASF biosecurity, making it a sufficiently promising model experiment for field application in ASF epidemic areas. However, this is still a vaccine variant, and further studies are planned to evaluate its genomic stability and transmissibility.

Indexed as

African Swine Fever Virus (ASFV)ASFV-G-ΔI177L/ΔLVRendemic controllive attenuated vaccineprotective efficacyrepeated exposure

Identifiers

PMID42506598
PMCPMC13419286

What OpenQuestion 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 OpenQuestion graph.