Evidence map›Paper›PMID 41441893›Full record

ArticleTropical animal health and production2025

ZnNPs and senps co-adjuvants deliver superior and long-lasting protection: first report in inactivated Rift Valley fever vaccines for sheep.

Sally Zaki Abdelrahman Hafez, Adel Abdelazim Fayed, Taradi Abdelfattah Sayed, Amany Dieb Bahr, Mohamed S Kamel

Abstract read
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Article in Tropical animal health and production, 2025. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sally Zaki Abdelrahman HafezRift Valley Fever Department, Vet. Serum and Vaccine Research Institute, Abbasia, Cairo, Egypt.
Adel Abdelazim FayedDepartment of Medicine and Infectious Diseases, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
Taradi Abdelfattah SayedRift Valley Fever Department, Vet. Serum and Vaccine Research Institute, Abbasia, Cairo, Egypt.
Amany Dieb BahrDepartment of Medicine and Infectious Diseases, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
Mohamed S KamelDepartment of Medicine and Infectious Diseases, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt. m_salah@cu.edu.eg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rift Valley Fever (RVF) poses a significant threat to livestock and human health, necessitating effective and safe vaccines. This study evaluated the immunogenicity and safety of novel inactivated RVF vaccines in sheep, enhanced with zinc oxide nanoparticles (ZnNPs) and selenium nanoparticles (SeNPs) as co-adjuvants, compared to an aluminum hydroxide gel (ALHV) adjuvanted vaccine alone. Our findings demonstrate that nanoparticle-formulated ALHV elicited a markedly faster onset of protection, achieving protective neutralizing antibody titers within 3–4 days post-vaccination, significantly accelerating immunity compared to approximately two weeks with ALHV alone. Furthermore, these enhanced formulations induced more robust and sustained humoral and IFN-γ responses, indicating superior activation of both antibody-mediated and cell-mediated immunity. The nanoparticle-enhanced vaccines also maintained long-lasting protection, extending the duration of protective antibody titers up to 11 months, compared to 10 months for ALHV alone. Beyond immunological benefits, these vaccines were safe, stable, and associated with improved growth performance in vaccinated sheep, particularly with ZnNPs. Biochemical analyses confirmed the absence of adverse effects on liver and kidney function, while showing beneficial increases in total protein and globulin levels. This study underscores the potential of SeNPs and ZnNPs as potent adjuvants for inactivated RVF vaccines, offering a promising strategy for developing more effective, rapidly protective, and durable vaccines against RVF and potentially other zoonotic diseases.

Indexed as

Adjuvants, ImmunologicAdjuvants, VaccineNanoparticlesRift Valley FeverSeleniumSheep DiseasesViral VaccinesZinc OxideAluminum HydroxideAnimalsAntibodies, ViralFemaleImmunity, CellularRift Valley fever virusSheepVaccinationAdjuvants, ImmunologicAdjuvants, VaccineAluminum HydroxideAntibodies, ViralSeleniumVaccines, InactivatedViral VaccinesZinc OxideImmunogenicityNanoparticle adjuvantsProtective immunityRift Valley feverSelenium nanoparticles (SeNPs)Zinc oxide nanoparticles (ZnNPs)

Identifiers

PMID41441893
PMCPMC12738598

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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.