Signorell Ladina M, Seitz Dominik, Merkel Sabina, Berger Rosemarie, Rudin Christoph
University Children's Hospital, Basel, Switzerland.
Pediatr Infect Dis J. 2006 Feb;25(2):123-8. doi: 10.1097/01.inf.0000195542.43369.96.
In the absence of mandatory nationwide toxoplasmosis screening during pregnancy in Switzerland, the Basel region introduced cord blood screening in 1982.
From 1982 to 1999, 64,622 cord blood samples (>90% of all neonates) collected in Basel region obstetric units were screened for toxoplasma specific immunoglobulin (Ig) G, M and A antibodies using commercial kits. Neonates with relevant results (IgG titers > or =300 IU/mL, or > or =200 IU/mL in the Abbott Toxo IMX system, and/or positive IgM or IgA antibodies) were monitored until clarification of infection status. From 1991 onward, retrospective maternal and follow-up data on these children were also collected by questionnaire.
Despite increasing maternal age, seroprevalence for toxoplasmosis decreased steadily from 53% (1982-1985) to 35% (1999). During the same period, the prevalence of congenital toxoplasmosis declined from 0.08% to 0.012%. IgM and/or IgA antibodies were present with the Platelia Toxo test (enzyme-linked immunosorbent assay; sanofi pasteur; Bio-Rad) in the cord blood samples of 17 of 18 infected neonates born between 1986 and 1999, regardless of maternal treatment in pregnancy. Vertical transmission rates in 69 women with proven or suspected primary infection between 1991 and 1999 were 3.9% with, compared to 27.7% without, antiparasitic treatment during pregnancy.
Toxoplasma seroprevalence and congenital toxoplasmosis incidence declined markedly in northwestern Switzerland from 1982 to 1999. Our data provide no conclusive evidence that maternal antiparasitic therapy in pregnancy affects vertical transmission because the treatment group also included women with suspected but unproven primary infection during pregnancy. Because toxoplasma specific IgA/IgM antibodies in cord blood identified almost all infected children, screening at birth may be more cost effective than during pregnancy.
在瑞士缺乏全国性孕期强制性弓形虫病筛查的情况下,巴塞尔地区于1982年引入了脐血筛查。
1982年至1999年期间,使用商业试剂盒对在巴塞尔地区产科单位采集的64622份脐血样本(超过所有新生儿的90%)进行弓形虫特异性免疫球蛋白(Ig)G、M和A抗体筛查。对结果相关的新生儿(IgG滴度≥300 IU/mL,或在雅培弓形虫IMX系统中≥200 IU/mL,和/或IgM或IgA抗体呈阳性)进行监测,直至感染状况明确。从1991年起,还通过问卷调查收集了这些儿童的回顾性母亲及随访数据。
尽管产妇年龄增加,但弓形虫病血清阳性率从1982 - 1985年的53%稳步下降至1999年的35%。同期,先天性弓形虫病的患病率从0.08%降至0.012%。在1986年至1999年出生的18例感染新生儿中,有17例的脐血样本通过普立泰科弓形虫检测(酶联免疫吸附测定;赛诺菲巴斯德;伯乐)检测出IgM和/或IgA抗体,无论母亲在孕期是否接受治疗。1991年至1999年期间,69例确诊或疑似原发性感染的女性中,孕期接受抗寄生虫治疗者垂直传播率为3.9%,未接受治疗者为27.7%。
1982年至1999年期间,瑞士西北部弓形虫血清阳性率和先天性弓形虫病发病率显著下降。我们的数据没有提供确凿证据表明孕期母亲抗寄生虫治疗会影响垂直传播,因为治疗组还包括孕期疑似但未经证实原发性感染的女性。由于脐血中弓形虫特异性IgA/IgM抗体几乎能识别所有受感染儿童,出生时筛查可能比孕期筛查更具成本效益。