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- W2004451401 endingPage "1233" @default.
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- W2004451401 abstract "Four individuals die from active TB disease each minute, while at least 2 billion are latently infected and at risk for disease reactivation. BCG, the only licensed TB vaccine, is effective in preventing childhood forms of TB; however its poor efficacy in adults, emerging drug-resistant TB strains and tedious chemotherapy regimes, warrant the development of novel prophylactic measures. Designing safe and effective vaccines against TB will require novel approaches on several levels, including the administration of rationally selected mycobacterial antigens in efficient delivery vehicles via optimal immunization routes. Given the primary site of disease manifestation in the lungs, development of mucosal immunization strategies to generate protective immune responses both locally, and in the circulation, may be important for effective TB prophylaxis. This review focuses on prime-boost immunization strategies currently under investigation and highlights the potential of mucosal delivery and rational vaccine design based on systems biology." @default.
- W2004451401 created "2016-06-24" @default.
- W2004451401 creator A5005601094 @default.
- W2004451401 creator A5026542621 @default.
- W2004451401 date "2012-10-01" @default.
- W2004451401 modified "2023-09-27" @default.
- W2004451401 title "Prime–boost approaches to tuberculosis vaccine development" @default.
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