Parker S P, Cubitt W D
Virology Department, Institute of Child Health, London.
J Clin Pathol. 1992 Oct;45(10):907-9. doi: 10.1136/jcp.45.10.907.
To determine whether the Eiken particle agglutination test could be modified to make it sufficiently sensitive to screen blood samples collected on Guthrie cards for the presence of antibodies to Toxoplasma gondii; to evaluate the specificity of the modified system; and to compare seroepidemiological data on the prevalence of T gondii in pregnant women.
Simulated dried blood spots were prepared from sera from pregnant women booking for antenatal care. Eluates from the simulated dried blood spot cards and sera were tested in parallel using the modified test (1 in 5 dilution of latex) and the standard assay (neat latex particles) and endpoints determined. Guthrie card eluates, from neonates in three Thames regions, were then tested using the modified test.
The modified test produced a 4.21-fold increase in antibody titre in 85 sera when tested in parallel with the standard test. Eluates of 168/170 from simulated dried blood spots derived from seropositive patients gave a positive result in the modified test. The two eluates which gave a negative result were derived from patients with an equivocal titre of 1/16 in the standard serum test. Of the eluates derived from serum negative patients all 103 were negative at a dilution of 1 in 4 in the modified test. The seroprevalence of antibodies to T gondii in pregnancy was 21.8% using the standard test. A similar value of 20.5% was obtained when dried blood spots from neonates in a similar region of London were tested by the modified test.
The modified Eiken Toxo-reagent test is sensitive, simple, and economic for screening large numbers of dried blood spots. The procedure could be easily semiautomated and the technique applied to the mass screening of neonatal blood samples collected on Guthrie cards to determine the seroprevalence of T gondii in pregnant women.
确定是否可以对艾肯颗粒凝集试验进行改进,使其具有足够的敏感性,用于筛查在古思里卡片上采集的血样中是否存在抗弓形虫抗体;评估改进系统的特异性;并比较孕妇弓形虫感染率的血清流行病学数据。
从预约产前检查的孕妇血清中制备模拟干血斑。使用改进试验(乳胶1:5稀释)和标准检测方法(纯乳胶颗粒)对模拟干血斑卡片洗脱液和血清进行平行检测,并确定终点。然后使用改进试验对来自三个泰晤士地区新生儿的古思里卡片洗脱液进行检测。
与标准试验平行检测时,改进试验使85份血清中的抗体滴度提高了4.21倍。来自血清阳性患者的168/170份模拟干血斑洗脱液在改进试验中呈阳性结果。两份呈阴性结果的洗脱液来自标准血清试验中滴度为1/16的可疑患者。在改进试验中,来自血清阴性患者的所有103份洗脱液在1:4稀释时均为阴性。使用标准试验时,孕妇抗弓形虫抗体的血清阳性率为21.8%。当使用改进试验对伦敦类似地区新生儿的干血斑进行检测时,得到了类似的20.5%的值。
改进的艾肯弓形虫试剂试验对于筛查大量干血斑具有敏感性、简便性和经济性。该程序可以很容易地实现半自动操作,并且该技术可应用于对在古思里卡片上采集的新生儿血样进行大规模筛查,以确定孕妇弓形虫的血清阳性率。