Evidence map›Paper›PMID 42787475›Full record

ArticleFrontiers in immunology2026

Safety and immunogenicity of a malignant catarrhal fever vaccine candidate expressing ovine gammaherpesvirus-2 glycoprotein B in cattle.

Daniela D Moré, Naomi S Taus, Katherine N Baker, Maria K Herndon, Reginaldo G Bastos, Benjamin G Dewals, Alain Vanderplasschen, Cristina W Cunha

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

8 authors.

Daniela D MoréAnimal Disease Research Unit, Agricultural Research Service, United States Department of Agriculture, Pullman, WA, United States.
Naomi S TausAnimal Disease Research Unit, Agricultural Research Service, United States Department of Agriculture, Pullman, WA, United States.
Katherine N BakerAnimal Disease Research Unit, Agricultural Research Service, United States Department of Agriculture, Pullman, WA, United States.
Maria K HerndonDepartment of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA, United States.
Reginaldo G BastosAnimal Disease Research Unit, Agricultural Research Service, United States Department of Agriculture, Pullman, WA, United States.
Benjamin G DewalsDepartment of Infectious and Parasitic Diseases, University of Liège, Liège, Belgium.
Alain VanderplasschenDepartment of Infectious and Parasitic Diseases, University of Liège, Liège, Belgium.
Cristina W CunhaAnimal Disease Research Unit, Agricultural Research Service, United States Department of Agriculture, Pullman, WA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Infection of susceptible livestock species, including domestic cattle and American bison, with ovine gammaherpesvirus-2 (OvHV-2), a gammaherpesvirus in the genus Macavirus, can result in an often-fatal disease known as sheep-associated malignant catarrhal fever (SA-MCF). Prevention of SA-MCF via vaccination is a key goal to support livestock producers. Methods: We assessed the safety and immunogenicity of a viral-vectored vaccine candidate consisting of a non-pathogenic recombinant alcelaphine gammaherpesvirus-1 expressing the OvHV-2 glycoprotein B (rAlHV-1/OvHV-2gB). The vaccine, formulated with an oil-in-water adjuvant, was administered intramuscularly to cattle using a prime-plus-two-boosters regimen. Results: Immunized animals did not develop MCF following rAlHV-1/OvHV-2gB inoculation. The vaccine virus did not establish persistent infection, and no viral shedding was detected after any immunization. Minor and transient adverse reactions associated with the adjuvant use were observed in some animals. Immunization with rAlHV-1/OvHV-2gB significantly altered the proportions of monocytes, T- and B- cells and induced the production of IFN-γ, CCL4, and CXCL10 in blood. Following Conclusion: Despite the need for further optimization of vaccine formulation and delivery, the rAlHV-1/OvHV-2gB vaccine elicited robust immune responses, supporting further evaluation of its protective efficacy in vaccine-challenge trials.

Indexed as

GammaherpesvirinaeHerpesvirus VaccinesImmunogenicity, VaccineMalignant CatarrhViral Envelope ProteinsViral VaccinesAnimalsAntibodies, NeutralizingAntibodies, ViralCattleSheepVaccinationAntibodies, NeutralizingAntibodies, ViralHerpesvirus VaccinesViral Envelope ProteinsViral Vaccinescattlecellular immunityglycoprotein Bhumoral immunitymalignant catarrhal feverovine gammaherpesvirus 2recombinant vaccine

Identifiers

PMID42787475
PMCPMC13601324

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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.