Evidence map›Paper›PMID 41584247›Full record

ArticleThe Canadian veterinary journal = La revue veterinaire canadienne2025

Comparing clinical and immunologic response efficacy of systemic prime

Nathan E N Erickson, Cheryl L Waldner, Michelle Sniatynski, Stacey Lacoste, Diego Moya, John A Ellis

Abstract read
In one paragraph

Article in The Canadian veterinary journal = La revue veterinaire canadienne, 2025. 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

6 authors.

Nathan E N EricksonDepartment of Large Animal Clinical Sciences (Erickson, Waldner, Moya) and Department of Veterinary Microbiology (Sniatynski, Lacoste, Ellis), Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4.
Cheryl L WaldnerDepartment of Large Animal Clinical Sciences (Erickson, Waldner, Moya) and Department of Veterinary Microbiology (Sniatynski, Lacoste, Ellis), Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4.
Michelle SniatynskiDepartment of Large Animal Clinical Sciences (Erickson, Waldner, Moya) and Department of Veterinary Microbiology (Sniatynski, Lacoste, Ellis), Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4.
Stacey LacosteDepartment of Large Animal Clinical Sciences (Erickson, Waldner, Moya) and Department of Veterinary Microbiology (Sniatynski, Lacoste, Ellis), Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4.
Diego MoyaDepartment of Large Animal Clinical Sciences (Erickson, Waldner, Moya) and Department of Veterinary Microbiology (Sniatynski, Lacoste, Ellis), Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4.
John A EllisDepartment of Large Animal Clinical Sciences (Erickson, Waldner, Moya) and Department of Veterinary Microbiology (Sniatynski, Lacoste, Ellis), Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study compared the efficacy of mucosal prime and systemic boost vaccination of young beef calves to the current industry standard of systemic prime in the presence of maternal antibodies. Animals: April-born commercial crossbred beef calves (N = 22) were enrolled as neonates with a mean body weight of 37.7 ± 5.3 kg. Procedure: At birth, 11 calves (PRB) were intranasally administered a commercial combination modified live virus [bovine herpesvirus type 1 (BoHV1), bovine respiratory syncytial virus (BRSV), bovine parainfluenza virus type 3 (BPIV3)] mucosal vaccine and 11 calves (INJ) remained unvaccinated. At ~39 ±2 d of age, all 22 calves were subcutaneously administered a combination modified live virus systemic vaccine (BoHV1, BRSV, BPIV3, and bovine viral diarrhea virus types 1 and 2). At weaning (159 ±2 d of age), calves were challenged by coinfection with BRSV and BPIV3 and monitored 8 d for health and immunologic outcomes. Results: The INJ group had an increased risk of greater group cumulative clinical scores on Day 8 and rectal temperature > 39.5°C on Days 7 and 8 post-challenge. The INJ calves had lower arterial oxygenation than the PRB on Day 6, indicating more severe lung pathology. Shedding of BRSV and BPIV3 was greater on Days 5 and 7 for INJ compared to PRB. Conclusion: Mucosal priming and systemic boosting resulted in fewer lung lesions and less shedding of virus post-viral challenge at weaning than systemic priming of young calves. Clinical relevance: Prime-boost vaccination optimizes immune development toward weaning.

Indexed as

Cattle DiseasesParainfluenza Virus 3, BovineRespiratory Syncytial Virus, BovineRespiratory Syncytial Virus InfectionsRespirovirus InfectionsVaccinationViral VaccinesAdministration, IntranasalAnimalsAnimals, NewbornAntibodies, ViralCattleCoinfectionFemaleMaleWeaningAntibodies, ViralViral Vaccines

Identifiers

PMID41584247
PMCPMC12825734

What OpenQuestion holds

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Read underepoch 390

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.