ArticleFrontiers in immunology2026
Development of Nipah virus mRNA vaccine for pandemic preparedness.
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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Nipah virus (NiV) is a highly pathogenic zoonotic virus associated with a high case fatality rate and human-to-human transmission, and it is listed as a priority pathogen by the World Health Organization (WHO) due to the lack of approved therapeutics or vaccines. NiV is classified as a biosafety level 4 (BSL-4) pathogen, which severely limits experimental studies in the absence of specialized containment facilities. Therefore, the establishment of pseudovirus-based surrogate models is essential for NiV vaccine research. Methods: In this study, single-antigen mRNA-lipid nanoparticle (mRNA-LNP) vaccines encoding the Nipah virus fusion protein (NiV-F) and attachment protein (NiV-G) were designed and evaluated using a co-administration strategy of independently formulated single-antigen mRNA-LNPs. A Vesicular stomatitis virus (VSV)-based NiV pseudovirus system was established and applied to assess neutralizing antibody responses in a mouse model. Results: The synthesized mRNA-LNP vaccines exhibited high purity and relatively consistent physicochemical properties, indicating uniform formulation characteristics. The VSV-based NiV pseudovirus showed a robust infection signal compared to background controls, and optimization of the purification process effectively reduced non-specific background, enabling reliable evaluation of Discussion: This study provides a foundation for future NiV mRNA-LNP vaccine development and presents a flexible vaccine design approach based on co-administration of independently formulated single-antigen mRNA-LNPs in which mixed administration of single-antigen mRNA-LNPs provides a flexible framework for independently modulating antigen composition and enabling antigen-specific immune responses. These findings provide a basis for future studies exploring diverse antigen combinations in NiV vaccine research.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.