Duffy K T, Wharton P J, Johnson J D, New L, Holliman R E
Public Health Laboratory Service, St George's Hospital, London.
J Clin Pathol. 1989 Dec;42(12):1291-5. doi: 10.1136/jcp.42.12.1291.
An immunoglobulin-M immunosorbent agglutination assay (ISAGA) was introduced to detect toxoplasma specific IgM. This assay incorporates mu chain capture and use of entire toxoplasma trophozoites as an antigen source. The performance of the ISAGA was compared with that of a double sandwich enzyme linked immunosorbent assay (DS-ELISA) currently used in the Public Health Laboratory Service Toxoplasma Reference Laboratories. The ISAGA was found to be more sensitive than DS-ELISA but there was no demonstrable difference in the specificity or reproducibility between the two assays. The ISAGA is suitable for the diagnosis of acute toxoplasmosis in immunocompetent patients and as a screening test for recent infection in pregnant women. The persistence of ISAGA reactivity, however, is such that additional serological assessment is required to define the risk of congenital infection.
引入了免疫球蛋白M免疫吸附凝集试验(ISAGA)来检测弓形虫特异性IgM。该试验采用μ链捕获法,并使用完整的弓形虫滋养体作为抗原来源。将ISAGA的性能与公共卫生实验室服务弓形虫参考实验室目前使用的双夹心酶联免疫吸附试验(DS-ELISA)进行了比较。发现ISAGA比DS-ELISA更敏感,但两种试验在特异性或可重复性方面没有明显差异。ISAGA适用于免疫功能正常患者急性弓形虫病的诊断,以及作为孕妇近期感染的筛查试验。然而,ISAGA反应性的持续存在使得需要进行额外的血清学评估来确定先天性感染的风险。