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Low-Avidity Autoantibodies against Bactericidal/Permeability-Increasing Protein Occur in Gram-Negative and
J Theprungsirikul1, J T Thaden2, R M Wierzbicki1
1Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire, USA.
Antibody autoreactivity against bactericidal/permeability-increasing protein (BPI) is linked to infections. Low-avidity anti-BPI IgG responses can occur acutely during bacteremia, not just with Pseudomonas aeruginosa, unlike chronic infections.
Area of Science:
- Immunology
- Microbiology
- Infectious Diseases
Background:
- Antibody autoreactivity against bactericidal/permeability-increasing protein (BPI) is associated with Pseudomonas aeruginosa infection in cystic fibrosis (CF), bronchiectasis (BE), and COPD.
- The pathogen-specific nature of BPI autoreactivity requires further investigation, particularly in acute bacteremic settings.
Purpose of the Study:
- To investigate the pathogen-specific nature of antibody autoreactivity against BPI in patients with bacteremia.
- To compare the avidity of anti-BPI IgG responses in acute bacteremia versus chronic respiratory infections.
Main Methods:
- Sera from five patient cohorts (n=214), including bacteremic patients (n=32), were analyzed for antibodies to BPI and bacterial antigens using ELISA.
- Autoantibody titers and avidity were measured. Antibody responses were correlated with bacterial culture results.
Main Results:
- Bacteremic patient sera showed significant IgG autoreactivity against BPI in infections with P. aeruginosa (64.7%) and Escherichia coli (46.7%).
- Anti-BPI IgG responses were observed in 14.9% of bacteremic patients, including those with Gram-positive bacteria like Staphylococcus aureus.
- Sera from bacteremic patients exhibited low-avidity anti-BPI IgG, contrasting with high-avidity responses seen in chronic respiratory infections.
Conclusions:
- Low-avidity anti-BPI IgG responses can be an acute response to bacteremia, irrespective of the specific pathogen.
- Chronic infection, particularly with P. aeruginosa, selects for high-avidity anti-BPI responses, suggesting implications for airway immunity.
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