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Author Correction:Multiscale dynamic immunomodulation by a nanoemulsified Trojan-TLR7/8 adjuvant for robust protection against heterologous pandemic and endemic viruses
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作者 Yeon Jeong Yoo Suhyeon Kim +12 位作者 asha wickramasinghe Jaemoo Kim JuA Song Young-Il Kim Juryeon Gil Young-Woock Noh Min-Ho Lee Sang-Seok Oh Myeong-Mi Lee Yebin Seong Jong-Soo Lee Young Ki Choi Yong Taik Lim 《Cellular & Molecular Immunology》 2025年第9期1128-1128,共1页
Correction to:Cellular&Molecular Immunology https://doi.org/10.1038/s41423-025-01306-6,published online 25 June 2025 In this article the author’s name Young Ki Choi was incorrectly written as Yong Ki Choi.The ori... Correction to:Cellular&Molecular Immunology https://doi.org/10.1038/s41423-025-01306-6,published online 25 June 2025 In this article the author’s name Young Ki Choi was incorrectly written as Yong Ki Choi.The original article has been corrected. 展开更多
关键词 cellular molecular immunology multiscale dynamic immunomodulation heterologous pandemic endemic viruses robust protection young ki choi nanoemulsified trojan tlr adjuvant
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Multiscale dynamic immunomodulation by a nanoemulsified Trojan-TLR7/8 adjuvant for robust protection against heterologous pandemic and endemic viruses
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作者 Yeon Jeong Yoo Suhyeon Kim +12 位作者 asha wickramasinghe Jaemoo Kim JuA Song Young-Il Kim Juryeon Gil Young-Woock Noh Min-Ho Lee Sang-Seok Oh Myeong-Mi Lee Yebin Seong Jong-Soo Lee Young Ki Choi Yong Taik Lim 《Cellular & Molecular Immunology》 2025年第9期1045-1060,共16页
The demand for safe vaccines that ensure long-term and broad protection against multiple viral variants has dramatically increased after the emergence of catastrophic infectious diseases such as COVID-19.To ensure lon... The demand for safe vaccines that ensure long-term and broad protection against multiple viral variants has dramatically increased after the emergence of catastrophic infectious diseases such as COVID-19.To ensure long-term and broad protection against heterologous virus variants,antigen-specific polyfunctional T cells should be orchestrated with the activation of follicular helper T(TFH)cells and germinal center(GC)B cells.Herein,we suggest a novel engineered nanoadjuvant(SE(Trojan-TLR7/8a))that enhances the migration of nonexhausted antigen-presenting cells(APCs)into lymph nodes and elicits the activation of TFH cells,the generation of GC B cells,and polyfunctional T cells via multiscale dynamic immunomodulation through squalene nanoemulsion(SE)-mediated macroscopic control of vaccine delivery and Trojan-TLR7/8a-enabled dynamic and sustained activation of APCs at the cellular level.SE(Trojan-TLR7/8a)can be lyophilized,reduce systemic toxicity,and outperform current commercial vaccine adjuvants(Alum or AS03)and mRNA vaccines.SE(Trojan-TLR7/8a)ensures cross-protection against diverse influenza and SARS-CoV-2 variants,providing 100%protection while maintaining a healthy state.SE(Trojan-TLR7/8a)also sustains a potent T-cell response in an aged ferret model of SFTSV infection.SE(Trojan-TLR7/8a)suggested herein provides a novel vaccine design principle for dynamic modulation at the multiscale level and demonstrates long-term and broad protective immunity against emerging pandemic and endemic infectious viruses. 展开更多
关键词 Dynamic immunomodulation Vaccine adjuvant NANOEMULSION TLR7/8 agonist Heterologous viruses
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