Evidence map›Paper›PMID 41680174›Full record

ArticleNPJ vaccines2026

Live-vectored antigen cocktail confers protection against African swine fever virus (ASFV) Georgia 2007/1 challenge.

Rakshith Kumar, Tae Kim, Michelle D Zajac, Bianca Libanori-Artiaga, Huldah Sang, Neha Sangewar, Emily Heitmann, Kumar Deepak, Jayden McCall, Leeanna Burton and 6 more

Abstract read
In one paragraph

Article in NPJ vaccines, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

16 authors.

Rakshith KumarDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Tae KimDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Michelle D ZajacDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Bianca Libanori-ArtiagaDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Huldah SangDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Neha SangewarDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Emily HeitmannDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Kumar DeepakDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Jayden McCallDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Leeanna BurtonDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Sally OlsonComparative Medicine Group, Kansas State University, Manhattan, KS, USA.
Shakirat AdetunjiDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Juergen A RichtDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Sabine E HammerDepartment of Biological Sciences and Pathobiology, University of Veterinary Medicine, Vienna, Austria.
Jessie D TrujilloDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Waithaka MwangiDepartment of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA. wmwangi@vet.k-state.edu.ORCID http://orcid.org/0000-0002-2705-7571

Funding

USDA National Institute of Food and Agriculture 2019-67015-29835
6 · The paper itself

Abstract

African swine fever (ASF) is a lethal disease of swine caused by the ASF virus (ASFV), for which no licensed vaccine is currently available in non-endemic countries. Here, replication-competent adenovirus-vectored ASFV multi-antigen constructs were shown to express ASFV antigens in primary swine cells. Pigs immunized with a cocktail of these constructs, with or without Quil-A adjuvant, tolerated the formulation well. The constructs elicited robust ASFV-specific IgG responses (p < 0.0001), which were boosted upon reimmunization (p < 0.05). Following challenge with the virulent ASFV Georgia 2007/1 strain using a natural transmission model, five of six pigs vaccinated without Quil-A survived, while all pigs receiving adjuvanted constructs succumbed to ASF. Survivors cleared the virus, exhibited only mild clinical signs, gained weight, and remained healthy for the remainder of the study. Histopathological analysis revealed an absence of ASFV-associated lesions in survivors, whereas severe lesions were observed in pigs vaccinated with adjuvanted constructs and in negative controls. Although neutralizing antibodies were undetectable, granzyme B-producing CD8α⁺ T cell responses were observed in survivors, indicating a likely correlation for cellular immunity in protection. These findings highlight the protective potential of ASFV antigen expression constructs and inform subunit vaccine design.

Identifiers

PMID41680174
PMCPMC13009383

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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.