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The Global Burden of Community-Acquired Pneumonia in Adults, Encompassing Invasive Pneumococcal Disease and the Prevalence of Its Associated Cardiovascular Events, with a Focus on Pneumolysin and Macrolide Antibiotics in Pathogenesis and Therapy

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出版社

MDPI
DOI: 10.3390/ijms241311038

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community-acquired pneumonia; cardiovascular events; dendritic cells; macrolides; macrophages; mannose receptor C-type1; platelets; pneumolysin; pro-inflammatory cytokines; Streptococcus pneumoniae

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Despite advances in therapies and vaccine technologies, community-acquired pneumonia (CAP) caused by Streptococcus pneumoniae remains a major global cause of infection-related mortality. Elderly individuals are particularly susceptible to invasive pneumococcal disease (IPD) which can lead to fatal cardiovascular events (CVEs). This review focuses on the prevalence and types of CVEs associated with bacterial CAP, especially IPD, and discusses the role of the pneumococcal toxin pneumolysin (Ply) in suppressing host immune defenses and promoting cardiac invasion. The review also covers the use of macrolide antibiotics in the treatment of bacterial CAP and mechanisms by which these agents inhibit Ply production in macrolide-resistant strains.
Despite innovative advances in anti-infective therapies and vaccine development technologies, community-acquired pneumonia (CAP) remains the most persistent cause of infection-related mortality globally. Confronting the ongoing threat posed by Streptococcus pneumoniae (the pneumococcus), the most common bacterial cause of CAP, particularly to the non-immune elderly, remains challenging due to the propensity of the elderly to develop invasive pneumococcal disease (IPD), together with the predilection of the pathogen for the heart. The resultant development of often fatal cardiovascular events (CVEs), particularly during the first seven days of acute infection, is now recognized as a relatively common complication of IPD. The current review represents an update on the prevalence and types of CVEs associated with acute bacterial CAP, particularly IPD. In addition, it is focused on recent insights into the involvement of the pneumococcal pore-forming toxin, pneumolysin (Ply), in subverting host immune defenses, particularly the protective functions of the alveolar macrophage during early-stage disease. This, in turn, enables extra-pulmonary dissemination of the pathogen, leading to cardiac invasion, cardiotoxicity and myocardial dysfunction. The review concludes with an overview of the current status of macrolide antibiotics in the treatment of bacterial CAP in general, as well as severe pneumococcal CAP, including a consideration of the mechanisms by which these agents inhibit the production of Ply by macrolide-resistant strains of the pathogen.

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