Evidence map›Paper›PMID 42115561›Full record

ArticlePharmaceutical research2026

Immune Efficacy of a Vaccine Candidate Based on Binding Protein 26 (BP26) from Brucella melitensis Encapsulated in Niosome Nanoparticles Against Brucellosis.

Kimia Talebi, Mohsen Chiani, Mehri Habibi, Morteza Samadi, M R Asadi Karam

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Article in Pharmaceutical research, 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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1 · What the graph read from it

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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.

Kimia TalebiDepartment of Immunology, Faculty of Medicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran.
Mohsen ChianiDepartment of Nanobiotechnology, New Technology Research Group, Pasteur Institute of Iran, Tehran, Iran.
Mehri HabibiDepartment of Medical Biotechnology, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Morteza SamadiDepartment of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran. samadi.for@gmail.com.
M R Asadi KaramDepartment of Molecular Biology, Pasteur Institute of Iran, Pasteur Ave, Tehran, 13164, Iran. m_asadi12@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBrucellosis is a common zoonosis, affecting animals and humans. Given the high prevalence of brucellosis, as well as the challenges associated with the animal vaccines, there is a need to develop effective vaccines against it. In this study, a Brucella vaccine candidate was developed based on niosome nanoparticles encapsulating BP26 protein from Brucella melitensis.

methodsCloning of amplified bp26 gene, cloning in pET28a-BL21 (DE3), and protein expression were done by optimized protocols. The properties of the synthesized niosome nanoparticles were evaluated using dynamic light scattering (DLS) and electron microscopy. Then, the entrapment efficacy, release profile, and effectiveness of BP26-encapsulated niosomes were assessed in vitro and in vivo.

resultsAnalyses indicated BP26-encapsulated niosomes with an average size of 265.5 nm, entrapment efficacy of 95.4%, and release rate of 27.4%. The BP26 encapsulated in niosome maintained the humoral immune responses up to 110 days after the initial vaccination in mice. Mice immunized with free BP26 and those receiving BP26.niosome had significantly higher levels of both IgG1 (Th2) and IgG2a (Th1) compared to the controls. In addition, mice vaccinated with niosome encapsulating BP26 produced higher IFN-γ and IL-2 cytokines as Th1 response indicators compared to BP26 alone, demonstrating the tendency of niosomes to switch the responses toward cellular immunity. Niosomes encapsulating BP26 could significantly protect the mice against Brucella melitensis.

conclusionsOur results suggest BP26-encapsulating niosome as a potential vaccine candidate for combating B. melitensis. However, further investigations are needed to present BP26.niosome as a promising Brucella vaccine for clinical trials.

Indexed as

Bacterial ProteinsBrucella melitensisBrucella VaccineBrucellosisNanoparticlesAnimalsAntibodies, BacterialFemaleImmunity, HumoralImmunoglobulin GLiposomesMembrane ProteinsMiceMice, Inbred BALB CNanovaccinesProtein Subunit VaccinesAntibodies, BacterialBacterial ProteinsBP26 protein, BrucellaBrucella VaccineImmunoglobulin GLiposomesMembrane ProteinsNanovaccinesProtein Subunit VaccinesBP26Brucella melitensisbrucellosisniosome nanoparticlesvaccine

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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.