» Articles » PMID: 31183393

OMIC Technologies and Vaccine Development: From the Identification of Vulnerable Individuals to the Formulation of Invulnerable Vaccines

Overview
Journal J Immunol Res
Publisher Wiley
Date 2019 Jun 12
PMID 31183393
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Routine vaccination is among the most effective clinical interventions to prevent diseases as it is estimated to save over 3 million lives every year. However, the full potential of global immunization programs is not realised because population coverage is still suboptimal. This is also due to the inadequate immune response and paucity of informative correlates of protection upon immunization of vulnerable individuals such as newborns, preterm infants, pregnant women, and elderly individuals as well as those patients affected by chronic and immune compromising medical conditions. In addition, these groups are undervaccinated for a number of reasons, including lack of awareness of vaccine-preventable diseases and uncertainty or misconceptions about the safety and efficacy of vaccination by parents and healthcare providers. The presence of these nonresponders/undervaccinated individuals represents a major health and economic burden to society, which will become particularly difficult to address in settings with limited public resources. This review describes innovative and experimental approaches that can help identify specific genomic profiles defining nonresponder individuals for whom specific interventions might be needed. We will provide examples that show how such information can be useful to identify novel biomarkers of safety and immunogenicity for future vaccine trials. Finally, we will discuss how system biology "OMICs" data can be used to design bioinformatic tools to predict the vaccination outcome providing genetic and molecular "signatures" of protective immune response. This strategy may soon enable identification of signatures highly predictive of vaccine safety, immunogenicity, and efficacy/protection thereby informing personalized vaccine interventions in vulnerable populations.

Citing Articles

Editorial: design considerations for future personalized vaccination approaches.

Rahman M Nanomedicine (Lond). 2024; 20(4):329-334.

PMID: 39552583 PMC: 11812407. DOI: 10.1080/17435889.2024.2419816.


Respiratory infection- and asthma-prone, low vaccine responder children demonstrate distinct mononuclear cell DNA methylation pathways.

Martino D, Schultz N, Kaur R, van Haren S, Kresoje N, Hoch A Clin Epigenetics. 2024; 16(1):85.

PMID: 38961479 PMC: 11223352. DOI: 10.1186/s13148-024-01703-0.


Vaccines against extraintestinal pathogenic (ExPEC): progress and challenges.

Qiu L, Chirman D, Clark J, Xing Y, Hernandez Santos H, Vaughan E Gut Microbes. 2024; 16(1):2359691.

PMID: 38825856 PMC: 11152113. DOI: 10.1080/19490976.2024.2359691.


Respiratory Infection- and Asthma-prone, Low Vaccine Responder Children Demonstrate Distinct Mononuclear Cell DNA Methylation Pathways.

Martino D, Schultz N, Kaur R, Haren S, Kresoje N, Hoch A Res Sq. 2024; .

PMID: 38645021 PMC: 11030504. DOI: 10.21203/rs.3.rs-4160354/v1.


Polyfunctional antibodies: a path towards precision vaccines for vulnerable populations.

Purcell R, Theisen R, Arnold K, Chung A, Selva K Front Immunol. 2023; 14:1183727.

PMID: 37600816 PMC: 10433199. DOI: 10.3389/fimmu.2023.1183727.


References
1.
Roodbari F, Roustai M, Mostafaie A, Soleimanjdahi H, Foroshani R, Sabahi F . Development of an enzyme-linked immunosorbent assay for immunoglobulin M antibodies against measles virus. Clin Diagn Lab Immunol. 2003; 10(3):439-42. PMC: 154957. DOI: 10.1128/cdli.10.3.439-442.2003. View

2.
Wernette C, Frasch C, Madore D, Carlone G, Goldblatt D, Plikaytis B . Enzyme-linked immunosorbent assay for quantitation of human antibodies to pneumococcal polysaccharides. Clin Diagn Lab Immunol. 2003; 10(4):514-9. PMC: 164258. DOI: 10.1128/cdli.10.4.514-519.2003. View

3.
Hunt D, Henderson R, Shabanowitz J, Sakaguchi K, Michel H, Sevilir N . Characterization of peptides bound to the class I MHC molecule HLA-A2.1 by mass spectrometry. Science. 1992; 255(5049):1261-3. DOI: 10.1126/science.1546328. View

4.
Ivanov A, Dragunsky E . ELISA as a possible alternative to the neutralization test for evaluating the immune response to poliovirus vaccines. Expert Rev Vaccines. 2005; 4(2):167-72. DOI: 10.1586/14760584.4.2.167. View

5.
Jacobson Vann J, Szilagyi P . Patient reminder and patient recall systems to improve immunization rates. Cochrane Database Syst Rev. 2005; (3):CD003941. PMC: 6485483. DOI: 10.1002/14651858.CD003941.pub2. View