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Mycobacteria

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Vaccines

Part of the book series: Handbook of Experimental Pharmacology ((HEP,volume 133))

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Abstract

Mycobacterium tuberculosis, the causative agent of tuberculosis, is expected to cause 30 million deaths in the coming 10 years — more than any other single infectious agent. The current vaccine against tuberculosis, bacille Calmette-Guérin (BCG), has a highly variable record of protection, and a widely accepted need exists for improved vaccines to control this disease. Infection with tuberculosis triggers a broad spectrum of immune responses which can contribute to elimination of the pathogen and to disease-associated pathology. In an ideal world a complete understanding of these responses would have provided an optimal rational design for improved prophylactic, or therapeutic, vaccines against tuberculosis and other mycobacterial diseases such as leprosy. However, the complexity of this immune response has thus far confronted us with a formidable obstacle, and novel vaccine strategies currently are still based on more pragmatic arguments. In the first part of this chapter we summarise the current knowledge of the host response to mycobacterial pathogens in order to highlight its complex role in protection and disease. The second part describes current approaches taken to produce novel, improved vaccines against mycobacterial pathogens.

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Janssen, R., Young, D., Thole, J. (1999). Mycobacteria. In: Perlmann, P., Wigzell, H. (eds) Vaccines. Handbook of Experimental Pharmacology, vol 133. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-59955-2_11

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