Center for Musculoskeletal Research, University of Rochester School of Medicine and Dentistry, 601 Elmwood Avenue, Box 665, Rochester, NY 14642. E-mail address for E.M. Schwarz: Edward
J Bone Joint Surg Am. 2013 Nov 20;95(22):e171. doi: 10.2106/JBJS.L.01654.
Staphylococcus aureus infections remain a major complication of orthopaedic surgery. Although serum C-reactive protein is useful for diagnosis, there are no specific tests for host immunity that can assess a patient's risk for serious infection. On the basis of the identification of glucosaminidase as a potentially protective antigen in animal models, we tested the hypotheses that anti-glucosaminidase IgG (immunoglobulin G) levels vary in sera of mice and orthopaedic patients with Staphylococcus aureus infections and that physical and neutralizing titers correlate.
In vitro ELISAs (enzyme-linked immunosorbent assays) were developed to quantify binding (physical) and enzyme-neutralizing (functional) anti-glucosaminidase IgG titers. The assays were validated with use of sera from naive, Staphylococcus aureus-challenged, and glucosaminidase-immunized mice. The physical, functional, and isotype titers of anti-glucosaminidase IgG were measured in sera from twenty-four patients with a confirmed Staphylococcus aureus infection following orthopaedic surgery and in sera from twenty noninfected patients. The specificity of the anti-glucosaminidase assay was evaluated by means of linear regression and receiver-operator characteristic curve analysis.
In mice, the analytic range of the physical titer assay for anti-glucosaminidase IgG was determined to be 1 ng/mL to 1 μg/mL, and physical titers correlated with functional titers (p < 0.002). Although all patients had measurable anti-glucosaminidase IgG, the physical titers in the infected patients were significantly higher by a factor of two compared with those in the healthy controls (p = 0.015). The physical titers were significantly correlated with the functional titers (p < 0.0001). Receiver-operator characteristic curve analysis demonstrated a diagnostic specificity of 0.72 (p = 0.014) for the assay. The anti-glucosaminidase titer in almost every patient was dominated by the IgG1 isotype.
Humoral immunity against glucosaminidase varied in mammals with Staphylococcus aureus osteomyelitis. Anti-glucosaminidase titers in sera were a potential biomarker of infection and have the potential to assess the quality of host immunity against Staphylococcus aureus.
Staphylococcus aureus infections can be challenging to diagnose, and there is no diagnostic test for host immunity. We demonstrated a cost-effective assay for determining the anti-glucosaminidase titer, which can be readily combined with conventional serology to improve diagnosis and to assess host immunity against Staphylococcus aureus.
金黄色葡萄球菌感染仍然是骨科手术的主要并发症。虽然血清 C 反应蛋白对于诊断很有用,但目前还没有专门用于评估患者发生严重感染风险的宿主免疫检测方法。基于鉴定出葡糖胺聚糖酶是动物模型中一种具有潜在保护作用的抗原,我们检验了以下假设:金黄色葡萄球菌感染的小鼠和骨科患者的血清中葡糖胺聚糖酶 IgG(免疫球蛋白 G)水平存在差异,并且物理和中和效价相关。
我们开发了体外 ELISA(酶联免疫吸附测定)来定量结合(物理)和酶中和(功能)的葡糖胺聚糖酶 IgG 效价。使用来自未受挑战的金黄色葡萄球菌、受到金黄色葡萄球菌挑战和葡糖胺聚糖酶免疫的小鼠的血清对该测定进行了验证。我们还测量了 24 例骨科手术后确诊金黄色葡萄球菌感染患者和 20 例非感染患者血清中的抗葡糖胺聚糖酶 IgG 的物理、功能和同种型效价。我们通过线性回归和接收者操作特征曲线分析评估了抗葡糖胺聚糖酶检测的特异性。
在小鼠中,抗葡糖胺聚糖酶 IgG 的物理效价测定的分析范围确定为 1 纳克/毫升至 1 微克/毫升,并且物理效价与功能效价相关(p < 0.002)。尽管所有患者均有可测量的抗葡糖胺聚糖酶 IgG,但感染患者的物理效价比健康对照组高两倍(p = 0.015)。物理效价与功能效价显著相关(p < 0.0001)。接收者操作特征曲线分析显示该检测的诊断特异性为 0.72(p = 0.014)。几乎每个患者的抗葡糖胺聚糖酶效价都主要由 IgG1 同种型主导。
哺乳动物的金黄色葡萄球菌骨髓炎存在针对葡糖胺聚糖酶的体液免疫。血清中的抗葡糖胺聚糖酶效价可能是感染的生物标志物,并有可能评估宿主对金黄色葡萄球菌的免疫质量。
金黄色葡萄球菌感染的诊断具有挑战性,目前还没有宿主免疫的诊断检测方法。我们展示了一种经济有效的测定抗葡糖胺聚糖酶效价的方法,该方法可以与常规血清学相结合,以改善诊断并评估宿主对金黄色葡萄球菌的免疫。