Evidence map›Paper›PMID 41653345›Full record

ArticleVeterinary research communications2026

Multivalent fowl Adenovirus-Newcastle disease vaccine: comprehensive evaluation in SPF and commercial broiler breeders.

Nahed Yahia, Ahmed Abdelhalim, Sara Hussein Mahmoud, Abdelhamid Bazid, Ravi Kumar, Hussein Aljassas, Maryam Alhnout, Dana Alhassan, Hussien Ali Hussien, Samah Eid and 1 more

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Article in Veterinary research communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Nahed YahiaReference Laboratory for Veterinary Quality Control on Poultry Production (RLQP), Animal Health Research Institute, Agriculture Research Centre (ARC), Giza, 12618, Egypt.
Ahmed AbdelhalimReference Laboratory for Veterinary Quality Control on Poultry Production (RLQP), Animal Health Research Institute, Agriculture Research Centre (ARC), Giza, 12618, Egypt.
Sara Hussein MahmoudCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, 12622, Egypt.
Abdelhamid BazidKlybeck Life Science Company, Dammam , 34848, Kingdom of Saudi Arabia.
Ravi KumarKlybeck Life Science Company, Dammam , 34848, Kingdom of Saudi Arabia.
Hussein AljassasKlybeck Life Science Company, Dammam , 34848, Kingdom of Saudi Arabia.
Maryam AlhnoutKlybeck Life Science Company, Dammam , 34848, Kingdom of Saudi Arabia.
Dana AlhassanKlybeck Life Science Company, Dammam , 34848, Kingdom of Saudi Arabia.
Hussien Ali HussienKlybeck Life Science Company, Dammam , 34848, Kingdom of Saudi Arabia.
Samah EidReference Laboratory for Veterinary Quality Control on Poultry Production (RLQP), Animal Health Research Institute, Agriculture Research Centre (ARC), Giza, 12618, Egypt.
Ahmed Aly KhalilVeterinary Serum and Vaccine Research Institute, Agricultural Research Center (ARC), Abbasia, Cairo, 11381, Egypt. ahme2001@gmail.com.ORCID http://orcid.org/0000-0002-2920-1178

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInclusion body hepatitis (IBH) and Newcastle disease (ND) impose substantial economic burdens on global poultry production, with combined annual losses exceeding $3 billion worldwide. Current vaccination strategies requiring separate immunizations increase handling stress and operational costs.

objectiveTo evaluate immunogenicity, cross-neutralization patterns, protective efficacy against virulent challenge, maternal antibody transfer, and commercial field performance of a novel multivalent inactivated vaccine containing fowl adenovirus (FAdV) serotypes 2, 8a, 8b, and 11 combined with Newcastle disease virus (NDV).

methodsTwo randomized, blinded, placebo-controlled trials were conducted: SPF trial (n = 200, Egypt) and commercial field trial (n = 120,000, Saudi Arabia). The multivalent vaccine contained inactivated FAdV serotypes 2, 8a, 8b, and 11 plus NDV strains, administered at 10 and 16 weeks of age with 24-week monitoring.

resultsVaccination induced robust antibody responses with FAdV ELISA geometric mean titers (GMT) reaching 22,847 (95% CI: 18,245 - 28,589) at weeks 4-6 post-primary vaccination, with peak anamnestic response of 28,945 (95% CI: 23,186 - 36,115) at week 8 following booster (p < 0.001) and NDV hemagglutination inhibition titers of 9.8 log₂ (95% CI: 8.4-11.4) (p < 0.001). Challenge studies demonstrated 96.7% protection against FAdV-2 (species D) (29/30 vaccinated vs. 6/30 controls; Fisher's exact p < 0.0001) and 100% protection against NDV (30/30 vs. 0/30). Maternal antibody transfer efficiency was 68.6% for IBH and 81.7% for NDV, with half-lives of 4.2 and 4.8 days respectively, providing 24-28 days and 21-24 days protection in progeny. Commercial field trial (120,000 birds) demonstrated 94.2% reduction in IBH mortality with 3.47:1 return on investment.

conclusionsThe multivalent IBH-NDV vaccine provides comprehensive immunological protection and consistent field efficacy. Although the cross-neutralization assay included representative serotypes, broader testing across additional field isolates is warranted to further define cross-protective breadth. Cross-neutralization analysis confirms the necessity of multivalent formulations due to type-specific immunity patterns, supporting implementation for integrated disease control in commercial broiler operations. This study provides a detailed evaluation of a quadrivalent FAdV-NDV inactivated vaccine demonstrating efficient maternal antibody transfer in broiler breeders.

Indexed as

Adenoviridae InfectionsAviadenovirusChickensNewcastle DiseaseNewcastle disease virusPoultry DiseasesViral VaccinesAnimalsAntibodies, ViralFemaleImmunity, Maternally-AcquiredSpecific Pathogen-Free OrganismsVaccinationVaccines, InactivatedAntibodies, ViralVaccines, InactivatedViral VaccinesBroiler breederCross-neutralizationFowl adenovirusInactivated vaccineInclusion body hepatitisMaternal antibody transferMultivalent vaccineNewcastle disease virusProtection kineticsSerotype-specific immunity

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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.