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Published on: April 7, 2015
Chlamydophila pneumoniae infection in patients undergoing carotid artery stent
F Mancini1, E Boatta, M F Vescio
1Istituto Superiore di Sanità, Dipartimento di Malattie Infettive, Parassitarie ed Immuno-mediate, Rome, Italy.
Insights
Chlamydophila pneumoniae (CP) infection is linked to symptomatic carotid artery disease. Stenting may reduce inflammation but not clear the persistent CP infection.
Area of Science:
- Infectious Diseases
- Cardiovascular Medicine
- Microbiology
Background:
- Chlamydophila pneumoniae (CP) infection is associated with cardiovascular conditions like carotid endarterectomy and coronary stenting.
- However, the relationship between CP and carotid artery stenting (CAS) remains unexplored.
Purpose of the Study:
- To investigate the presence and impact of Chlamydophila pneumoniae infection in patients undergoing carotid artery stenting.
- To assess the correlation between CP infection markers and symptomatic versus asymptomatic carotid artery disease.
Main Methods:
- Evaluated 47 patients (27 symptomatic, 20 asymptomatic) before and after CAS intervention.
- Assessed for Chlamydophila pneumoniae DNA, anti-CP IgG and IgA antibodies, and chlamydial HSP60 (Cp-HSP60) antibodies.
Main Results:
- CP DNA and antibodies were predominantly found in symptomatic patients before stenting.
- Following CAS, CP DNA and Cp-HSP60 antibodies decreased significantly in positive cases.
- CP IgA antibodies showed persistence, indicating no significant change post-intervention.
Conclusions:
- Chlamydophila pneumoniae infection plays a significant role in symptomatic carotid artery disease patients.
- Carotid artery stenting may contribute to the resolution of inflammation associated with CP infection.
- Stent placement does not appear to eliminate persistent Chlamydophila pneumoniae infection.
Abstract:
Although several reports have correlated Chlamydophila pneumoniae (CP) infection with carotid endarterectomy and coronary stent, no data have been reported on the potential relationship between this pathogen and carotid artery stenting (CAS). Hence, we evaluated 47 subjects, 27 symptomatic and 20 asymptomatic, before CAS intervention and during the follow up, for the presence of CP DNA and anti-CP antibodies, including chlamydial HSP60 (Cp-HSP60). Before stent placement, CP DNA was detected exclusively in symptomatic patients, all of whom were also positive for CP IgG and IgA and 85.7 percent of them also had CP-HSP60 antibodies. At the follow-up, all CP DNA positive and 11 out of the 13 symptomatic patients with Cp-HSP60 antibodies became negatives. In contrast, no change was observed for CP- IgA antibodies. Despite the small number of patients, the present study advocates an important role of CP infection in symptomatic patients with carotid artery disease. Our findings also suggest that stent placement and/or therapy might have a role in favouring resolution of inflammation, though not affecting persistence of CP infection.
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