The Application of Single-Cell Technologies for Vaccine Development Against Viral Infections.

Publication date: Jun 26, 2025

The development of vaccines against viral infections has advanced rapidly over the past century, propelled by innovations in laboratory and molecular technologies. These advances have expanded the range of vaccine platforms beyond live-attenuated and inactivated vaccines to include recombinant platforms, such as subunit proteins and virus-like particles (VLPs), and more recently, mRNA-based vaccines, while also enhancing methods for evaluating vaccine performance. Despite these innovations, a persistent challenge remains: the inherent complexity and heterogeneity of immune responses continue to impede efforts to achieve consistently effective and durable protection across diverse populations. Single-cell technologies have emerged as transformative tools for dissecting this immune heterogeneity, providing comprehensive and granular insights into cellular phenotypes, functional states, and dynamic host-pathogen interactions. In this review, we examine how single-cell epigenomic, transcriptomic, proteomic, and multi-omics approaches are being integrated across all stages of vaccine development-from infection-informed discovery to guide vaccine design, to high-resolution evaluation of efficacy, and refinement of cell lines for manufacturing. Through representative studies, we highlight how insights from these technologies contribute to the rational design of more effective vaccines and support the development of personalized vaccination strategies.

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Concepts Keywords
High COVID-19
Host infectious diseases
Inactivated influenza
Transcriptomic mRNA
Vaccines multi-omics
recombinant protein
single-cell technology
vaccine development
viral diseases
virus-like particles (VLPs)

Semantics

Type Source Name
disease IDO cell
disease MESH Viral Infections
disease IDO host
disease IDO pathogen
disease MESH infection
disease IDO protein
disease MESH infectious diseases
disease MESH influenza
disease MESH COVID 19
disease MESH smallpox
disease MESH polio
disease MESH cowpox
drug DRUGBANK Oxygen
disease MESH plague
disease IDO bacteria
drug DRUGBANK Formaldehyde
disease IDO assay
disease IDO nucleic acid
pathway KEGG Viral replication
drug DRUGBANK Nonoxynol-9
disease IDO immunodeficiency
disease MESH hepatitis
disease IDO production
pathway REACTOME Immune System
drug DRUGBANK Isoxaflutole
pathway REACTOME Apoptosis
drug DRUGBANK Coenzyme M
pathway REACTOME Methylation
disease IDO susceptibility
drug DRUGBANK Pentaerythritol tetranitrate
disease IDO pathogen host
pathway REACTOME Digestion
drug DRUGBANK Cycloserine
drug DRUGBANK Hepatitis B Vaccine (Recombinant)
disease MESH kidney failure
disease IDO adaptive immune response
pathway REACTOME Adaptive Immune System
disease MESH Histocompatibility
drug DRUGBANK Succimer
disease IDO process
drug DRUGBANK Esomeprazole
disease IDO blood
disease MESH PRRs
disease IDO immune response
disease MESH inflammation
disease MESH respiratory infections
disease MESH hypoxia
disease MESH oxidative stress
pathway REACTOME Translation
disease MESH viral shedding
disease IDO role
disease MESH measles
pathway KEGG Measles
disease MESH rabies
disease MESH breakthrough infection
drug DRUGBANK Creatinolfosfate
pathway REACTOME Metabolism
pathway KEGG mTOR signaling pathway
drug DRUGBANK Iron
disease MESH dengue
disease MESH coad
drug DRUGBANK Aluminum hydroxide
pathway REACTOME Acetylation
disease MESH anaphylaxis
disease MESH myocarditis
disease MESH autoimmune hepatitis
disease IDO symptom
disease MESH drug induced liver injury
pathway KEGG Platelet activation
disease MESH neoplasms
drug DRUGBANK Methylergometrine
drug DRUGBANK Methotrexate
disease IDO immunosuppression
drug DRUGBANK Tretamine

Original Article

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