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Molecular Pathology of Rickettsial Lung Infections

Rickettsial infections of humans comprise a diverse group of infections caused by pathogens that are obligate intracellular bacteria with a genetic relationship, including the genera Rickettsia, Orientia, Ehrlichia, and Anaplasma. The host cells of these pathogens largely belie the systemic clinical...

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Autor principal: Dumler, J. Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147442/
http://dx.doi.org/10.1007/978-0-387-72430-0_38
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author Dumler, J. Stephen
author_facet Dumler, J. Stephen
author_sort Dumler, J. Stephen
collection PubMed
description Rickettsial infections of humans comprise a diverse group of infections caused by pathogens that are obligate intracellular bacteria with a genetic relationship, including the genera Rickettsia, Orientia, Ehrlichia, and Anaplasma. The host cells of these pathogens largely belie the systemic clinical manifestations, because Rickettsia and Orientia infect endothelial cells, and Ehrlichia and Anaplasma infect circulating leukocytes (monocytes and neutrophils, respectively). Thus, the predominant manifestations (fever, headache, myalgia, with or without rash) do not usually focus attention on the respiratory system; however, the underlying pathogenesis of these infections involves degrees of vascular compromise either by direct injury and inflammation or by the action of vasoactive proinflammatory molecules such as cytokines, chemokines, and prostaglandins. Given that the lung possesses the largest vascular bed in the human body, it is not surprising that pulmonary involvement is periodically identified and, when severely affected, is considered a potentially life-threatening complication.1,2
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spelling pubmed-71474422020-04-10 Molecular Pathology of Rickettsial Lung Infections Dumler, J. Stephen Molecular Pathology of Lung Diseases Article Rickettsial infections of humans comprise a diverse group of infections caused by pathogens that are obligate intracellular bacteria with a genetic relationship, including the genera Rickettsia, Orientia, Ehrlichia, and Anaplasma. The host cells of these pathogens largely belie the systemic clinical manifestations, because Rickettsia and Orientia infect endothelial cells, and Ehrlichia and Anaplasma infect circulating leukocytes (monocytes and neutrophils, respectively). Thus, the predominant manifestations (fever, headache, myalgia, with or without rash) do not usually focus attention on the respiratory system; however, the underlying pathogenesis of these infections involves degrees of vascular compromise either by direct injury and inflammation or by the action of vasoactive proinflammatory molecules such as cytokines, chemokines, and prostaglandins. Given that the lung possesses the largest vascular bed in the human body, it is not surprising that pulmonary involvement is periodically identified and, when severely affected, is considered a potentially life-threatening complication.1,2 2010-05-21 /pmc/articles/PMC7147442/ http://dx.doi.org/10.1007/978-0-387-72430-0_38 Text en © Springer Science+Business Media, LLC. 2008 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Dumler, J. Stephen
Molecular Pathology of Rickettsial Lung Infections
title Molecular Pathology of Rickettsial Lung Infections
title_full Molecular Pathology of Rickettsial Lung Infections
title_fullStr Molecular Pathology of Rickettsial Lung Infections
title_full_unstemmed Molecular Pathology of Rickettsial Lung Infections
title_short Molecular Pathology of Rickettsial Lung Infections
title_sort molecular pathology of rickettsial lung infections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147442/
http://dx.doi.org/10.1007/978-0-387-72430-0_38
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