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Clinical manifestations and immune response to tuberculosis

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SPRINGER
DOI: 10.1007/s11274-023-03636-x

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Tuberculosis; Immune response; Mycobacterium tuberculosis; Clinical manifestations

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Tuberculosis is a widespread and highly impactful disease, ranking among the top ten causes of death worldwide. Despite a large number of individuals being carriers of the tuberculosis bacillus, only a third of them develop active disease. This can be attributed to the differential immune response of hosts, involving cellular and humoral components, as well as cytokines and chemokines. Understanding the relationship between clinical manifestations of tuberculosis and the immune response can provide insights into the pathophysiological and immunological mechanisms of the disease.
Tuberculosis is a far-reaching, high-impact disease. It is among the top ten causes of death worldwide caused by a single infectious agent; 1.6 million tuberculosis-related deaths were reported in 2021 and it has been estimated that a third of the world's population are carriers of the tuberculosis bacillus but do not develop active disease. Several authors have attributed this to hosts' differential immune response in which cellular and humoral components are involved, along with cytokines and chemokines. Ascertaining the relationship between TB development's clinical manifestations and an immune response should increase understanding of tuberculosis pathophysiological and immunological mechanisms and correlating such material with protection against Mycobacterium tuberculosis. Tuberculosis continues to be a major public health problem globally. Mortality rates have not decreased significantly; rather, they are increasing. This review has thus been aimed at deepening knowledge regarding tuberculosis by examining published material related to an immune response against Mycobacterium tuberculosis, mycobacterial evasion mechanisms regarding such response and the relationship between pulmonary and extrapulmonary clinical manifestations induced by this bacterium which are related to inflammation associated with tuberculosis dissemination through different routes.

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