
Department of Internal Medicine, Yeungnam University College of Medicine, Daegu, Korea
© 2025 Yeungnam University College of Medicine, Yeungnam University Institute of Medical Science
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Conflicts of interest
No potential conflict of interest relevant to this article was reported.
Acknowledgments
The author thanks Skywork.ai, Dr. Yong-Geun Jung, and Mr. Justin Cho for their contributions in structuring, organizing references, and proofreading the language of this work. And the author appreciates the Yeungnam University College of Medicine research support team for providing the illustrations used in this study.
Funding
None.
| Vaccine type | Representative vaccine | Mechanism of immune induction | Advantages | Limitations |
|---|---|---|---|---|
| Inactivated vaccine | Sinopharm, Sinovac | Injection of chemically inactivated virus | High safety; established technology | Weaker immune response; requires adjuvants and possibly boosters |
| → induces antibody production | ||||
| Protein subunit vaccine | Novavax | Injection of purified viral proteins | Low adverse effects; high safety | Weak immunogenicity alone; adjuvants required |
| → induces antibodies and some T cell response | ||||
| Non-replicating viral vector | AstraZeneca, Sputnik V, Johnson & Johnson | Vector virus delivers antigen gene | Strong antibody and T cell responses | Pre-existing immunity to vector may reduce efficacy |
| → antigen produced in host cells | ||||
| Replicating viral vector | NDV-based, Measles-VSV platforms | Replicating vector expresses antigen | Induces strong immunity, including mucosal | Limited safety data; still in early development |
| → mucosal and systemic immune response | ||||
| mRNA vaccine | Pfizer-BioNTech, Moderna | mRNA in lipid nanoparticles | Rapid development; robust immune response | Requires cold storage; potential for reactogenicity |
| → intracellular antigen expression | ||||
| DNA vaccine | ZyCoV-D (India) | Plasmid DNA delivers antigen gene | Thermostable; scalable and cost-effective production | Lower immunogenicity in humans; needs delivery system (e.g., electroporation) |
| → antigen expression in host cells |
NDV, Newcastle disease virus; mRNA, messenger RNA.