Chadha Ashley D, Thomsen Isaac P, Jimenez-Truque Natalia, Soper Nicole R, Jones Lauren S, Sokolow Andrew G, Torres Victor J, Creech C Buddy
Department 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.
Department of Pediatrics, Division of Infectious Diseases, The Monroe Carell, Jr. Children's Hospital at Vanderbilt and the Vanderbilt University School of Medicine, Nashville, Tennessee.
J Cyst Fibros. 2016 Sep;15(5):597-604. doi: 10.1016/j.jcf.2015.12.023. Epub 2016 Jan 25.
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.
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.
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.
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.
金黄色葡萄球菌是最早定植于囊性纤维化患儿肺部的细菌病原体之一,也是肺部病情加重的重要原因。囊性纤维化患者对金黄色葡萄球菌的适应性宿主反应仍未得到充分阐明,对发病机制和潜在干预措施具有重要意义。本研究的目的是确定囊性纤维化患儿对特定葡萄球菌外毒素(LukAB、α-溶血素和杀白细胞素)的功能性抗体反应,并评估这种反应与肺部病情加重的关系。
招募了50名囊性纤维化患儿,并对其进行了为期12个月的前瞻性随访。在常规就诊和肺部病情加重期间评估临床特征和血清学特征,并进行功能性抗体评估以测量对LukAB介导的细胞毒性的中和作用。
对于每种抗原,如果在病情加重时检测到金黄色葡萄球菌,几何平均滴度显著更高。对于LukAB,病情加重随访时的几何平均滴度显著高于病情加重期间的滴度,这与人类疾病期间的表达一致,并且体液反应能够中和LukAB介导的细胞毒性。此外,肺部病情加重期间金黄色葡萄球菌培养阳性与LukA滴度≥1:160的几率高31倍相关,表明该检测方法具有潜在的诊断能力。
白细胞毒素LukAB由金黄色葡萄球菌表达,并在囊性纤维化肺部感染的情况下被人类适应性免疫反应识别。抗LukAB抗体不仅可预测病情加重期间金黄色葡萄球菌培养阳性,而且在中和这种毒素方面具有功能。