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This analysis uncovers the complex host-pathogen interaction in tuberculosis, suggesting systems biology can transform our understanding of immune responses.
Tuberculosis is once again the most fatal global infectious disease and has killed many more humans than any other pathogen. Despite the identification of Mycobacterium tuberculosis (Mtb) over 140 years ago, we have yet to control the epidemic. A central issue is the complexity of the host-pathogen interaction, with diverse immunological routes leading to tuberculosis disease. This intricate relationship results from the prolonged co-evolution of the pathogen with humans, potentially due to Mtb exposure giving a survival advantage. Emerging methodologies, such as single cell and spatial transcriptomics, offer a golden opportunity to understand the immunology unpinning this host-pathogen interaction at unprecedented resolution. However, these analyses will be fundamentally flawed if they do not consider the intricacies of human Mtb infection. Here, we propose that attempts to find single unifying immunological mechanisms of tuberculosis are hindering progress, and we must embrace the complexity of multiple paths to disease to allow the systems biology era to deliver transformative solutions.
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Reichmann et al. (2025) studied this question.
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