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Updated: Mar 26, 2026

Quantifying the Cytotoxicity of Staphylococcus aureus Against Human Polymorphonuclear Leukocytes
Published on: January 3, 2020
Host response to Staphylococcus aureus cytotoxins in children with cystic fibrosis
Ashley D Chadha1, Isaac P Thomsen2, Natalia Jimenez-Truque2
1Department of Pediatrics, Division of Allergy, Immunology, and Pulmonary Medicine, The Monroe Carell, Jr. Children's Hospital at Vanderbilt and the Vanderbilt University School of Medicine, Nashville, Tennessee.
Insights
The study found that anti-LukAB antibodies in children with cystic fibrosis can neutralize Staphylococcus aureus leukotoxin LukAB. These antibodies also help predict S. aureus infections during pulmonary exacerbations.
Area of Science:
- Immunology
- Microbiology
- Pediatrics
Background:
- Staphylococcus aureus is a key pathogen in pediatric cystic fibrosis lung infections.
- Pulmonary exacerbations in cystic fibrosis are often linked to S. aureus.
- The host's adaptive immune response to S. aureus in cystic fibrosis is not fully understood.
Purpose of the Study:
- To assess the functional antibody response to staphylococcal exotoxins (LukAB, alpha-hemolysin, PVL) in children with cystic fibrosis.
- To investigate the correlation between antibody response and pulmonary exacerbations.
- To evaluate the neutralizing capacity of antibodies against LukAB.
Main Methods:
- Prospective follow-up of 50 children with cystic fibrosis for 12 months.
- Assessment of clinical data and serologic profiles during routine visits and exacerbations.
- Functional antibody assays to measure neutralization of LukAB-mediated cytotoxicity.
Main Results:
- Antibody titers against S. aureus antigens were higher during exacerbations.
- Anti-LukAB antibody titers increased after exacerbations, indicating a functional immune response.
- A titer of anti-LukAB ≥1:160 was associated with a 31-fold increased likelihood of S. aureus detection during exacerbations.
Conclusions:
- Leukotoxin LukAB from S. aureus is recognized by the human adaptive immune system in cystic fibrosis lung infections.
- Anti-LukAB antibodies are predictive of S. aureus presence during exacerbations.
- These antibodies demonstrate functional neutralization of LukAB toxicity.
Background:
Staphylococcus aureus is one of the earliest bacterial pathogens to colonize the lungs of children with cystic fibrosis and is an important contributor to pulmonary exacerbations. The adaptive host response to S. aureus in cystic fibrosis remains inadequately defined and has important implications for pathogenesis and potential interventions. The objectives of this study were to determine the functional antibody response to select staphylococcal exotoxins (LukAB, alpha-hemolysin, and PVL) in children with cystic fibrosis and to evaluate the relationship of this response with pulmonary exacerbations.
Methods:
Fifty children with cystic fibrosis were enrolled and followed prospectively for 12months. Clinical characteristics and serologic profiles were assessed at routine visits and during pulmonary exacerbations, and functional antibody assessments were performed to measure neutralization of LukAB-mediated cytotoxicity.
Results:
For each antigen, geometric mean titers were significantly higher if S. aureus was detected at the time of exacerbation. For LukAB, geometric mean titers were significantly higher at exacerbation follow-up compared to titers during the exacerbation, consistent with expression during human disease, and the humoral response capably neutralized LukAB-mediated cytotoxicity. Moreover, the presence of a positive S. aureus culture during a pulmonary exacerbation was associated with 31-fold higher odds of having a LukA titer ≥1:160, suggesting potential diagnostic capability of this assay.
Conclusions:
The leukotoxin LukAB is expressed by S. aureus and recognized by the human adaptive immune response in the setting of pulmonary infection in cystic fibrosis. Anti-LukAB antibodies were not only predictive of positive staphylococcal culture during exacerbation, but also functional in the neutralization of this toxin.
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