» Articles » PMID: 27157411

Vaccine Technologies: From Whole Organisms to Rationally Designed Protein Assemblies

Overview
Date 2016 May 10
PMID 27157411
Citations 95
Authors
Affiliations
Soon will be listed here.
Abstract

Vaccines have been the single most significant advancement in public health, preventing morbidity and mortality in millions of people annually. Vaccine development has traditionally focused on whole organism vaccines, either live attenuated or inactivated vaccines. While successful for many different infectious diseases whole organisms are expensive to produce, require culture of the infectious agent, and have the potential to cause vaccine associated disease in hosts. With advancing technology and a desire to develop safe, cost effective vaccine candidates, the field began to focus on the development of recombinantly expressed antigens known as subunit vaccines. While more tolerable, subunit vaccines tend to be less immunogenic. Attempts have been made to increase immunogenicity with the addition of adjuvants, either immunostimulatory molecules or an antigen delivery system that increases immune responses to vaccines. An area of extreme interest has been the application of nanotechnology to vaccine development, which allows for antigens to be expressed on a particulate delivery system. One of the most exciting examples of nanovaccines are rationally designed protein nanoparticles. These nanoparticles use some of the basic tenants of structural biology, biophysical chemistry, and vaccinology to develop protective, safe, and easily manufactured vaccines. Rationally developed nanoparticle vaccines are one of the most promising candidates for the future of vaccine development.

Citing Articles

Designing a potent multivalent epitope vaccine candidate against via reverse vaccinology technique - bioinformatics and immunoinformatic approach.

Panda S, Swain S, Sahu B, Mahapatra S, Dey J, Sarangi R Front Immunol. 2025; 16:1513245.

PMID: 40018038 PMC: 11865050. DOI: 10.3389/fimmu.2025.1513245.


Hybrid Predictive Machine Learning Model for the Prediction of Immunodominant Peptides of Respiratory Syncytial Virus.

Bukhari S, Ogudo K Bioengineering (Basel). 2024; 11(8).

PMID: 39199749 PMC: 11351268. DOI: 10.3390/bioengineering11080791.


Advances in the study of LNPs for mRNA delivery and clinical applications.

Wang B, Shen B, Xiang W, Shen H Virus Genes. 2024; 60(6):577-591.

PMID: 39172354 DOI: 10.1007/s11262-024-02102-6.


Protein Nanoparticles as Vaccine Platforms for Human and Zoonotic Viruses.

Pandey K, Sahoo B, Pattnaik A Viruses. 2024; 16(6).

PMID: 38932228 PMC: 11209504. DOI: 10.3390/v16060936.


Immunoinformatics Design and In Vivo Immunogenicity Evaluation of a Conserved CTL Multi-Epitope Vaccine Targeting HPV16 E5, E6, and E7 Proteins.

Guo N, Niu Z, Yan Z, Liu W, Shi L, Li C Vaccines (Basel). 2024; 12(4).

PMID: 38675774 PMC: 11053576. DOI: 10.3390/vaccines12040392.


References
1.
Jung J, Nagaraj A, Fox E, Rudra J, Devgun J, Collier J . Co-assembling peptides as defined matrices for endothelial cells. Biomaterials. 2009; 30(12):2400-10. PMC: 2677558. DOI: 10.1016/j.biomaterials.2009.01.033. View

2.
Kumar Gupta S, Bajwa P, Deb R, Chellappa M, Dey S . Flagellin a toll-like receptor 5 agonist as an adjuvant in chicken vaccines. Clin Vaccine Immunol. 2014; 21(3):261-70. PMC: 3957660. DOI: 10.1128/CVI.00669-13. View

3.
Means T, Hayashi F, Smith K, Aderem A, Luster A . The Toll-like receptor 5 stimulus bacterial flagellin induces maturation and chemokine production in human dendritic cells. J Immunol. 2003; 170(10):5165-75. DOI: 10.4049/jimmunol.170.10.5165. View

4.
Fine P, Eames K, Heymann D . "Herd immunity": a rough guide. Clin Infect Dis. 2011; 52(7):911-6. DOI: 10.1093/cid/cir007. View

5.
Lu J, Wang X, Marin-Muller C, Wang H, Lin P, Yao Q . Current advances in research and clinical applications of PLGA-based nanotechnology. Expert Rev Mol Diagn. 2009; 9(4):325-41. PMC: 2701163. DOI: 10.1586/erm.09.15. View