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一种源自刚地弓形虫微线体 8 的肽,具有血清学证据,可区分近期和慢性人类感染。

A peptide originated from Toxoplasma gondii microneme 8 displaying serological evidence to differentiate recent from chronic human infection.

机构信息

Laboratory of Immunoparasitology, Institute of Biomedical Sciences, Federal University of Uberlândia, 38400-902 Uberlândia, Minas Gerais, Brazil; Laboratory of Biology, Federal University of Vales do Jequitinhonha e Mucuri, Campus Janaúba, Janaúba, Minas Gerais, Brazil.

Laboratory of Immunoparasitology, Institute of Biomedical Sciences, Federal University of Uberlândia, 38400-902 Uberlândia, Minas Gerais, Brazil.

出版信息

Parasitol Int. 2021 Oct;84:102394. doi: 10.1016/j.parint.2021.102394. Epub 2021 May 24.

Abstract

Toxoplasmosis is able to cause death and/or sequelae in foetuses from pregnant women and immunocompromised individuals. The early diagnosis, able to differentiate acute from chronic phases, is essential to define the treatment against this disease and minimize the risk of complications. Here we describe a peptide derived from microneme 8 (pMIC8) protein of Toxoplasma gondii, able to distinguish the phase of infection. By using human and mice serum samples with different infection times, we assessed the ability of pMIC8 to interact with antibodies present in early of infection, and compared the results obtained with soluble antigen of T. gondii (STAg). The results showed that pMIC8 was recognized more precisely with antibodies present in serum samples from individuals with time of infection below 3 months, followed by those between 4 and 6 months of infection. Based on these results, it is possible to conclude that the association of immunoassays using STAg and pMIC8 as antigen preparations can be used to distinguish acute from chronic infections.

摘要

弓形虫病能够导致孕妇和免疫功能低下者的胎儿死亡和/或后遗症。早期诊断能够区分急性和慢性阶段,对于确定针对这种疾病的治疗方法和最大限度地降低并发症的风险至关重要。在这里,我们描述了一种来源于刚地弓形虫微线体 8 蛋白(pMIC8)的肽,它能够区分感染阶段。通过使用具有不同感染时间的人和小鼠血清样本,我们评估了 pMIC8 与感染早期存在的抗体相互作用的能力,并将结果与刚地弓形虫可溶性抗原(STAg)进行了比较。结果表明,pMIC8 能够更准确地识别感染时间在 3 个月以下的个体血清样本中的抗体,其次是感染时间在 4 至 6 个月之间的个体。基于这些结果,可以得出结论,使用 STAg 和 pMIC8 作为抗原制剂的免疫分析的联合应用可以用于区分急性和慢性感染。

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