J Lavanya Agnes Angalene, Pa Paopachapich, Seng Chheng Y, Rhee Joon Haeng, Lee Shee Eun
Department of Biomedical Sciences, Chonnam National University, Hwasun-gun, Republic of Korea.
Combinatorial Tumor Immunotherapy MRC, Chonnam National University Medical School, Hwasun-gun, Jeonnam, Republic of Korea.
Hum Vaccin Immunother. 2025 Dec;21(1):2492906. doi: 10.1080/21645515.2025.2492906. Epub 2025 May 12.
Mucosal infectious diseases represent a significant global health burden, impacting millions of people worldwide through pathogens that invade the respiratory, gastrointestinal, and urogenital tracts. Mucosal vaccines provide a promising strategy to combat these diseases by preventing pathogens from entering through the portals as well as within the systemic response compartment. However, challenges such as antigen instability, inefficient delivery, suboptimal immune activation, and the complex biology of mucosal barriers hinder their development. These limitations require integrating specialized adjuvants and delivery systems. Protein nanocages, self-assembling nanoscale structures that can be engineered, may provide an innovative solution for co-delivering antigens and adjuvants. With their remarkable stability, biocompatibility, and design versatility, protein nanocages can potentially overcome existing challenges in mucosal vaccine delivery and enhance protective immune responses. This review highlights the potential of protein nanocages to revolutionize mucosal vaccine development by addressing these challenges.
粘膜感染性疾病是一项重大的全球健康负担,通过侵入呼吸道、胃肠道和泌尿生殖道的病原体影响着全球数百万人。粘膜疫苗提供了一种有前景的策略来对抗这些疾病,通过防止病原体通过这些门户进入以及在全身反应区室内部进入。然而,诸如抗原不稳定性、递送效率低下、免疫激活不理想以及粘膜屏障的复杂生物学特性等挑战阻碍了它们的发展。这些限制需要整合专门的佐剂和递送系统。蛋白质纳米笼是可以进行工程设计的自组装纳米级结构,可能为共递送抗原和佐剂提供一种创新解决方案。凭借其卓越的稳定性、生物相容性和设计多功能性,蛋白质纳米笼有可能克服粘膜疫苗递送中现有的挑战并增强保护性免疫反应。本综述强调了蛋白质纳米笼通过应对这些挑战来彻底改变粘膜疫苗开发的潜力。