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

dc.contributor.authorAnderson, Ronald
dc.contributor.authorFeldman, Charles
dc.contributor.emailronald.anderson@up.ac.zaen_US
dc.date.accessioned2024-05-23T11:34:19Z
dc.date.available2024-05-23T11:34:19Z
dc.date.issued2023-07
dc.description.abstractDespite 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.en_US
dc.description.departmentImmunologyen_US
dc.description.sdgSDG-03:Good heatlh and well-beingen_US
dc.description.sdgSDG-10:Reduces inequalitiesen_US
dc.description.urihttps://www.mdpi.com/journal/ijmsen_US
dc.identifier.citationAnderson, R.; Feldman, C. 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. International Journal of Molecular Sciences 2023, 24, 11038. https://doi.org/10.3390/ijms241311038.en_US
dc.identifier.issn1661-6596 (print)
dc.identifier.issn1422-0067 (online)
dc.identifier.other10.3390/ijms241311038
dc.identifier.urihttp://hdl.handle.net/2263/96202
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.rights© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en_US
dc.subjectDendritic cellsen_US
dc.subjectMacrolidesen_US
dc.subjectMacrophagesen_US
dc.subjectMannose receptor C-type1en_US
dc.subjectPlateletsen_US
dc.subjectPneumolysinen_US
dc.subjectPro-inflammatory cytokinesen_US
dc.subjectStreptococcus pneumoniaeen_US
dc.subjectCommunity-acquired pneumonia (CAP)en_US
dc.subjectInvasive pneumococcal disease (IPD)en_US
dc.subjectCardiovascular event (CVE)en_US
dc.subjectSDG-03: Good health and well-beingen_US
dc.titleThe 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 therapyen_US
dc.typeArticleen_US

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Anderson_Global_2023.pdf
Size:
367.72 KB
Format:
Adobe Portable Document Format
Description:
Article

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: