Micronanoparticled risedronate exhibits potent vaccine adjuvant effects
Journal of Controlled Release, ISSN: 0168-3659, Vol: 365, Page: 369-383
2024
- 2Citations
- 8Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations2
- Citation Indexes2
- Captures8
- Readers8
Article Description
Micro/Nano-scale particles are widely used as vaccine adjuvants to enhance immune response and improve antigen stability. While aluminum salt is one of the most common adjuvants approved for human use, its immunostimulatory capacity is suboptimal. In this study, we modified risedronate, an immunostimulant and anti-osteoporotic drug, to create zinc salt particle-based risedronate (Zn-RS), also termed particulate risedronate. Compared to soluble risedronate, micronanoparticled Zn-RS adjuvant demonstrated increased recruitment of innate cells, enhanced antigen uptake locally, and a similar antigen depot effect as aluminum salt. Furthermore, Zn-RS adjuvant directly and quickly stimulated immune cells, accelerated the formulation of germinal centers in lymph nodes, and facilitated the rapid production of antibodies. Importantly, Zn-RS adjuvant exhibited superior performance in both young and aged mice, effectively protecting against respiratory diseases such as SARS-CoV-2 challenge. Consequently, particulate risedronate showed great potential as an immune-enhancing vaccine adjuvant, particularly beneficial for vaccines targeting the susceptible elderly.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0168365923007423; http://dx.doi.org/10.1016/j.jconrel.2023.11.025; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85178380571&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37972764; https://linkinghub.elsevier.com/retrieve/pii/S0168365923007423; https://dx.doi.org/10.1016/j.jconrel.2023.11.025
Elsevier BV
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