Stanley Division of Developmental Neurovirology, Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.
Microbes Infect. 2013 Jan;15(1):74-83. doi: 10.1016/j.micinf.2012.10.016. Epub 2012 Nov 7.
To distinguish active from inactive/chronic infection in Toxoplasma gondii-seropositive individuals, we have developed an enzyme-linked immunosorbent assay (ELISA) using specific peptides derived from Toxoplasma matrix antigen MAG1. We used this assay to measure matrix specific antibodies and pilot studies with infected mice established the validity of two peptides. The immune response against MAG1 occurs in about 12 days postinfection and displays a sex difference later on in mouse model, with males producing higher antibody titers than females. Serum samples from 22 patients with clinical toxoplasmosis and from 26 patients with serological evidence of past exposure to Toxoplasma (more than one year infection history) were analyzed. Both MAG1 peptides detected antibodies significant frequently and robustly from active stage than from the chronic stage of toxoplasmosis. The results indicate that both MAG1 peptides may be used as a tool to differentiate active from inactive infection. It also may be considered in the design of potential vaccines in humans.
为了区分弓形体病血清阳性个体中的活动性/慢性感染,我们使用源自弓形体质膜抗原 MAG1 的特异性肽段开发了一种酶联免疫吸附试验(ELISA)。我们使用该检测方法测量基质特异性抗体,并用感染小鼠进行的初步研究证实了两种肽段的有效性。针对 MAG1 的免疫反应在感染后约 12 天发生,并在后续的小鼠模型中表现出性别差异,雄性产生的抗体滴度高于雌性。分析了来自 22 例临床弓形体病患者和 26 例血清学证据表明过去接触过弓形体(感染病史超过一年)的患者的血清样本。与慢性阶段相比,两种 MAG1 肽都能更频繁且更有力地检测到来自活动性阶段的抗体。这些结果表明,两种 MAG1 肽都可以用作区分活动性和非活动性感染的工具。在设计人类潜在疫苗时也可以考虑使用这两种肽段。