Advances in vaccine adjuvant development and future perspectives

dc.contributor.authorSinani, Genada
dc.contributor.authorŞenel, Sevda
dc.date.accessioned2025-08-14T17:35:21Z
dc.date.available2025-08-14T17:35:21Z
dc.date.issued2025
dc.departmentFakülteler, Eczacılık Fakültesi
dc.descriptionArticle number : 2517137 CODEN : DDELE
dc.description.abstractUse of highly purified antigens to improve vaccine safety has led to reduced immunogenicity and efficacy, resulting in the need for adjuvants to increase and/or modulate the immunogenicity of the vaccine. Despite the need for potent and safe vaccine adjuvants, currently, there are still very few adjuvants in licensed human vaccines. Advances in immunology and molecular biology, especially in the last decade, have allowed researchers to understand better how the adjuvants work and enhance immune responses. While aluminum salts are still the most widely used adjuvants, research has shifted toward the rational design of adjuvant systems containing immunostimulatory molecules. Application of systems biology, which is based on high-throughput technologies using mathematical and computational modeling, has provided a deeper understanding of the biological events elicited by vaccination as well as the influence of other factors such as sex, age, microbiota, genetics and metabolism on the immune response. By this means, it became possible to tailor potential vaccine adjuvants more precisely for a successful vaccine with enhanced efficacy, safety and protection. In this review, after describing the mechanism of action of the adjuvants, current adjuvants in licensed vaccines, as well as those under clinical development will be mentioned in detail. Finally, new approaches in vaccine adjuvant development using systems biology and artificial intelligence will be reviewed, and future directions in vaccine research in regard to efficacy, safety and quality aspects will be discussed.
dc.identifier.citationSinani, G., & Şenel, S. (2025). Advances in vaccine adjuvant development and future perspectives. Drug Delivery, 32(1), 2517137. 10.1080/10717544.2025.2517137
dc.identifier.doi10.1080/10717544.2025.2517137
dc.identifier.issn1071-7544
dc.identifier.issue1
dc.identifier.pmid40536024
dc.identifier.scopus2-s2.0-105008518009
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://hdl.handle.net/20.500.12939/5893
dc.identifier.volume32
dc.identifier.wosWOS:001511949800001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakPubMed
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.institutionauthorSinani, Genada
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofDrug Delivery
dc.relation.publicationcategoryDiğer
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectClinical trials
dc.subjectlicensed vaccine adjuvants
dc.subjectmechanism of action
dc.subjectmetabolic and epigenetic adjuvants
dc.subjectmicrobiota
dc.subjectsystems biology
dc.subjecttissue-resident memory responses
dc.titleAdvances in vaccine adjuvant development and future perspectives
dc.typeArticle

Dosyalar

Orijinal paket
Listeleniyor 1 - 1 / 1
Yükleniyor...
Küçük Resim
İsim:
Tam Metin / Full Text
Boyut:
2.99 MB
Biçim:
Adobe Portable Document Format
Lisans paketi
Listeleniyor 1 - 1 / 1
[ X ]
İsim:
license.txt
Boyut:
1.17 KB
Biçim:
Item-specific license agreed upon to submission
Açıklama: