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Elimination of the cold-chain dependence of a nanoemulsion adjuvanted vaccine against tuberculosis by lyophilization

机译:通过冻干消除纳米乳液佐剂疫苗对结核的冷链依赖性

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摘要

Next-generation rationally-designed vaccine adjuvants represent a significant breakthrough to enable development of vaccines against challenging diseases including tuberculosis, HIV, and malaria. New vaccine candidates often require maintenance of a cold-chain process to ensure long-term stability and separate vials to enable bedside mixing of antigen and adjuvant. This presents a significant financial and technological barrier to worldwide implementation of such vaccines. Herein we describe the development and characterization of a tuberculosis vaccine comprised of both antigen and adjuvant components that are stable in a single vial at sustained elevated temperatures. Further this vaccine retains the ability to elicit both antibody and TH1 responses against the vaccine antigen and protect against experimental challenge with Mycobacterium tuberculosis. These results represent a significant breakthrough in the development of vaccine candidates that can be implemented throughout the world without being hampered by the necessity of a continuous cold chain or separate adjuvant and antigen vials.
机译:下一代经过合理设计的疫苗佐剂代表着一项重大突破,可以开发出针对结核病,HIV和疟疾等挑战性疾病的疫苗。新的候选疫苗通常需要维持冷链过程以确保长期稳定性,并需要分离小瓶以使抗原和佐剂在床旁混合。这为在全球范围内实施此类疫苗提出了重大的财务和技术障碍。本文中,我们描述了由抗原和佐剂成分组成的结核疫苗的开发和表征,该抗原和佐剂成分在持续升高的温度下可在单个小瓶中稳定。此外,这种疫苗保留了引发针对疫苗抗原的抗体和TH1反应的能力,并能抵抗结核分枝杆菌的实验性攻击。这些结果代表了候选疫苗开发的重大突破,该候选疫苗可以在全世界范围内实施,而不受连续冷链或分离的佐剂和抗原小瓶的必要性的影响。

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