Permutations of time and place in tuberculosis
Permutations of time and place in tuberculosis
Tuberculosis remains a global health pandemic. The current depiction of the Mycobacterium tuberculosis life cycle proposes that airborne bacilli are inhaled and phagocytosed by alveolar macrophages, resulting in the formation of a granuloma that ruptures into the airways to reinitiate the infectious cycle. However, this widely proposed model overlooks the fact, established 100 years ago, that the initial site of M tuberculosis implantation is in the lower zones of the lungs, whereas infectious cavitary pulmonary disease develops at the lung apices. The immunological events at these two pulmonary locations are different—cavitation only occurs in the apices and not in the bases. Yet the current conceptual model of tuberculosis renders the immunology of these two temporally and spatially separated events identical. One key consequence is that prevention of primary childhood tuberculosis at the lung bases is regarded as adequate immunological protection, but extensive evidence shows that greater immunity could predispose to immunopathology and transmission at the lung apex. A much greater understanding of time and place in the immunopathological mechanisms underlying human tuberculosis is needed before further pre-exposure vaccination trials can be done
1357-1360
Elkington, P.T.
60828c7c-3d32-47c9-9fcc-6c4c54c35a15
Friedland, J.S.
e64a7af8-b969-4426-82e6-5ebe819799c9
November 2015
Elkington, P.T.
60828c7c-3d32-47c9-9fcc-6c4c54c35a15
Friedland, J.S.
e64a7af8-b969-4426-82e6-5ebe819799c9
Abstract
Tuberculosis remains a global health pandemic. The current depiction of the Mycobacterium tuberculosis life cycle proposes that airborne bacilli are inhaled and phagocytosed by alveolar macrophages, resulting in the formation of a granuloma that ruptures into the airways to reinitiate the infectious cycle. However, this widely proposed model overlooks the fact, established 100 years ago, that the initial site of M tuberculosis implantation is in the lower zones of the lungs, whereas infectious cavitary pulmonary disease develops at the lung apices. The immunological events at these two pulmonary locations are different—cavitation only occurs in the apices and not in the bases. Yet the current conceptual model of tuberculosis renders the immunology of these two temporally and spatially separated events identical. One key consequence is that prevention of primary childhood tuberculosis at the lung bases is regarded as adequate immunological protection, but extensive evidence shows that greater immunity could predispose to immunopathology and transmission at the lung apex. A much greater understanding of time and place in the immunopathological mechanisms underlying human tuberculosis is needed before further pre-exposure vaccination trials can be done
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e-pub ahead of print date: 28 August 2015
Published date: November 2015
Organisations:
Clinical & Experimental Sciences
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Local EPrints ID: 381234
URI: http://eprints.soton.ac.uk/id/eprint/381234
ISSN: 1473-3099
PURE UUID: c9cfb664-b580-4218-91d8-2a052e6e144e
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Date deposited: 01 Oct 2015 09:07
Last modified: 15 Mar 2024 03:43
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Author:
J.S. Friedland
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