TY - JOUR
T1 - The sixth revolution in pediatric vaccinology
T2 - immunoengineering and delivery systems
AU - Soni, Dheeraj
AU - Bobbala, Sharan
AU - Li, Sophia
AU - Scott, Evan A.
AU - Dowling, David J.
N1 - Funding Information:
The authors D.S. and D.J.D. would like to thank Dr. Ofer Levy for his mentorship, and Boston Children’s Hospital Precision Vaccines Program for publication support. This work was supported by U.S. National Institutes of Health grant 1R21AI137932-01A1 and Adjuvant Discovery Program 75N93019C00044. All figures for this review have been created with BioRender.
Publisher Copyright:
© 2020, The Author(s).
PY - 2021/5
Y1 - 2021/5
N2 - Abstract: Infection is the predominant cause of mortality in early life, and immunization is the most promising biomedical intervention to reduce this burden. However, very young infants fail to respond optimally to most vaccines currently in use, especially neonates. In 2005, Stanley Plotkin proposed that new delivery systems would spur a new revolution in pediatric vaccinology, just as attenuation, inactivation, cell culture of viruses, genetic engineering, and adjuvantation had done in preceding decades. Recent advances in the field of immunoengineering, which is evolving alongside vaccinology, have begun to increasingly influence vaccine formulation design. Historically, the particulate nature of materials used in many vaccine formulations was empiric, often because of the need to stabilize antigens or reduce endotoxin levels. However, present vaccine delivery systems are rationally engineered to mimic the size, shape, and surface chemistry of pathogens, and are therefore often referred to as “pathogen-like particles”. More than a decade from his original assessment, we re-assess Plotkin’s prediction. In addition, we highlight how immunoengineering and advanced delivery systems may be uniquely capable of enhancing vaccine responses in vulnerable populations, such as infants. Impact: Immunoengineering and advanced delivery systems are leading to new developments in pediatric vaccinology.Summarizes delivery systems currently in use and development, and prospects for the future.Broad overview of immunoengineering’s impact on vaccinology, catering to Pediatric Clinicians and Immunologists.
AB - Abstract: Infection is the predominant cause of mortality in early life, and immunization is the most promising biomedical intervention to reduce this burden. However, very young infants fail to respond optimally to most vaccines currently in use, especially neonates. In 2005, Stanley Plotkin proposed that new delivery systems would spur a new revolution in pediatric vaccinology, just as attenuation, inactivation, cell culture of viruses, genetic engineering, and adjuvantation had done in preceding decades. Recent advances in the field of immunoengineering, which is evolving alongside vaccinology, have begun to increasingly influence vaccine formulation design. Historically, the particulate nature of materials used in many vaccine formulations was empiric, often because of the need to stabilize antigens or reduce endotoxin levels. However, present vaccine delivery systems are rationally engineered to mimic the size, shape, and surface chemistry of pathogens, and are therefore often referred to as “pathogen-like particles”. More than a decade from his original assessment, we re-assess Plotkin’s prediction. In addition, we highlight how immunoengineering and advanced delivery systems may be uniquely capable of enhancing vaccine responses in vulnerable populations, such as infants. Impact: Immunoengineering and advanced delivery systems are leading to new developments in pediatric vaccinology.Summarizes delivery systems currently in use and development, and prospects for the future.Broad overview of immunoengineering’s impact on vaccinology, catering to Pediatric Clinicians and Immunologists.
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U2 - 10.1038/s41390-020-01112-y
DO - 10.1038/s41390-020-01112-y
M3 - Review article
C2 - 32927471
AN - SCOPUS:85090992895
SN - 0031-3998
VL - 89
SP - 1364
EP - 1372
JO - Pediatric research
JF - Pediatric research
IS - 6
ER -