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The diversity of latent TB

BMC Proceedings
Springer (Biomed Central Ltd.)
Publication Date
  • Oral Presentation
  • Biology
  • Medicine


The diversity of latent TB ORAL PRESENTATION Open Access The diversity of latent TB Douglas Young From Immunodiagnosis of Tuberculosis: New Questions, New Tools Virginia, VA, USA. 21-23 September 2008 During the second half of the twentieth century, researchers have been focused on breaking down science into small pieces, and in doing so have learned that understanding the small pieces does not necessarily translate into a greater understanding of the whole. Sys- tems biology has emerged as a way of understanding these systems in total, but requires scientists to work through complexity to arrive at a greater understanding. To understand the fundamental biology of TB, scientists must first understand the biology of latent TB: why the bacteria are able to resist the host’s ability to eradicate them over a long period of time. The commonly-used definition of latent TB—antigen-specific T-cell response without clinical symptoms—is very broad and may in fact lead us away from the consideration that latent TB may not be the same in every patient. Does everyone infected with latent TB harbor viable bacteria? Where are these bacteria in the body and what are they doing? As part of the Grand Challenges in Global Health Pro- gram, a Gates Foundation-funded initiative to develop drugs for latent TB, our team is working with a hypoxia model, based on the idea that the bacteria encounters an environment (hypoxia) in the host which is hostile. In response, the bacteria may switch to a slowly-repli- cating persistent phenotype that makes them more drug-tolerant. We are also using live-imaging to study lesions in active latent TB in both humans and primates to identify what the bacteria are doing in different types of lesions, why some bacteria are immunologically active and others dormant. Based on our findings to date, biomarkers in addition to T-cell response must be identified in order to develop a better understanding of what is happening in patients with latent TB. We hypothesize that

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