2019
DOI: 10.1016/j.biomaterials.2019.119308
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Silver nanoparticle-adjuvanted vaccine protects against lethal influenza infection through inducing BALT and IgA-mediated mucosal immunity

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Cited by 60 publications
(36 citation statements)
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“…This vaccine which was made from inactivated S. aureus in combination with AgNO 3 , has been shown to be more effective than a vaccine with S. aureus alone and has led to an increase in T-cell and B-cell counts while raising the rate of phagocytes and antibodies in the mice blood serum. Also, the positive effects of such nanoparticles on the respiratory viruses have been demonstrated [39,40]. Furthermore, it has been shown that when nanoparticles are used as adjuvants in vaccine production, they lead to increased antigen presentation and stronger immunity than common adjuvants [40,41].…”
Section: Discussionmentioning
confidence: 99%
“…This vaccine which was made from inactivated S. aureus in combination with AgNO 3 , has been shown to be more effective than a vaccine with S. aureus alone and has led to an increase in T-cell and B-cell counts while raising the rate of phagocytes and antibodies in the mice blood serum. Also, the positive effects of such nanoparticles on the respiratory viruses have been demonstrated [39,40]. Furthermore, it has been shown that when nanoparticles are used as adjuvants in vaccine production, they lead to increased antigen presentation and stronger immunity than common adjuvants [40,41].…”
Section: Discussionmentioning
confidence: 99%
“…In the process of vaccination, the utilizing of vaccine adjuvants and follow-up evaluations are very critical. For instance, silver NPs can be deployed as an adjuvant in mucosal vaccines based on inactivated influenza virus, which stimulates the remarkable antigen specific IgA formation with low toxicity by stimulating bronchus-associated lymphoid tissue (BALT) neogenesis [127]. Additionally, in one study, gold NPs and toll-like receptor agonists (applied as operative adjuvant in UV-inactivated SARS-CoV vaccine) were investigated as vaccine adjuvants for application with recombinant S protein [50].…”
Section: Covs and Nanovaccinesmentioning
confidence: 99%
“…35 There are a number of exciting tissue-engineered human in vitro lung models currently available that could be leveraged for studying viral infection 36,37 and established in vivo models for respiratory viruses, including NHPs, already in use. [38][39][40] Elements that may improve the relevance of in vitro models include: (1) human rather than animal cell lines; (2) co-culture of multiple pulmonary cell lines; (3) 3D scaffolds that mimic native pulmonary architecture; and (4) culture methods that permit generation of ECM prior to viral inoculation. Additional head-to-head studies will need to be performed to determine if these components are necessary to capture the pathophysiology of viral infection.…”
Section: In Vitro Modelsmentioning
confidence: 99%
“…71 Silver nanoparticles have also been used to deliver inactivated influenza vaccine locally with some specificity to lung immune cells, resulting in greater IgG titers and reduced mortality in a murine model. 40 While there are currently fewer studies regarding coronavirus vaccines, there has been some success in mice in which nanoparticles were prepared from a SARS-CoV-1 peptide sequence, and subsequent sera was successful in preventing infection of Vero cells. 72 In addition to various particle-based platforms, tissue engineering strategies have been harnessed to create scaffold systems for vaccination enhancement.…”
Section: Vaccine Platformsmentioning
confidence: 99%