Schwingel Johanna M, Edwards Katie J, Cox Andrew D, Masoud Hussein, Richards James C, St Michael Frank, Tekwe Carmen D, Sethi Sanjay, Murphy Timothy F, Campagnari Anthony A
Department of Microbiology and Immunology, University at Buffalo, Buffalo, NY 14214, USA.
Infect Immun. 2009 Oct;77(10):4548-58. doi: 10.1128/IAI.00294-09. Epub 2009 Aug 3.
Moraxella catarrhalis is a causative agent of otitis media in children and lower respiratory tract infections in adults suffering from chronic obstructive pulmonary disease (COPD). This strict human pathogen continues to be a significant cause of disease in this broad spectrum of patients because there is no available vaccine. Although numerous putative vaccine antigens have been described, little is known about the human immune response to M. catarrhalis infection in vivo. Human serum antibodies are directed at a number of surface proteins, and lipooligosaccharides (LOS) and detoxified LOS may be an effective immunogen in mice. In this study, we used a specific LOS-based enzyme-linked immunosorbent assay (ELISA), containing the three major M. catarrhalis serotypes together with a complete series of truncated LOS mutants, to detect the development of new antibodies to specific regions of the oligosaccharide molecule. We compared serum samples from COPD patients who had recently cleared an M. catarrhalis infection to serum samples collected prior to their infection. Variability in the antibody response to LOS was observed, as some patients developed serotype-specific antibodies, others developed antibodies to the LOS of each serotype, others developed broadly cross-reactive antibodies, and some did not develop new antibodies. These newly developed human antibodies are directed at both side chains and core structures in the LOS molecule. This LOS-based ELISA can be used to dissect the human antibody response to both internal and external carbohydrate epitopes, thus providing a better understanding of the humoral immune response to M. catarrhalis LOS epitopes developed during natural infection.
卡他莫拉菌是儿童中耳炎以及患有慢性阻塞性肺疾病(COPD)的成人下呼吸道感染的病原体。由于没有可用疫苗,这种严格的人类病原体在这类广泛患者群体中仍是一个重要的致病因素。尽管已经描述了许多假定的疫苗抗原,但对于人类在体内对卡他莫拉菌感染的免疫反应却知之甚少。人血清抗体针对多种表面蛋白,脂寡糖(LOS)和解毒的LOS在小鼠中可能是一种有效的免疫原。在本研究中,我们使用了一种基于特定LOS的酶联免疫吸附测定(ELISA),该测定包含三种主要的卡他莫拉菌血清型以及一系列完整的截短LOS突变体,以检测针对寡糖分子特定区域的新抗体的产生。我们将近期清除了卡他莫拉菌感染的COPD患者的血清样本与其感染前采集的血清样本进行了比较。观察到对LOS的抗体反应存在差异,一些患者产生了血清型特异性抗体,另一些患者产生了针对每种血清型LOS的抗体,还有一些患者产生了广泛交叉反应的抗体,而有些患者则未产生新抗体。这些新产生的人抗体针对LOS分子中的侧链和核心结构。这种基于LOS的ELISA可用于剖析人类对内部和外部碳水化合物表位的抗体反应,从而更好地了解在自然感染期间对卡他莫拉菌LOS表位的体液免疫反应。