Garcia L S, Shimizu R Y
Clinical Microbiology, Department of Pathology and Laboratory Medicine, University of California at Los Angeles Medical Center, 90095-1713, USA.
J Clin Microbiol. 1997 Jun;35(6):1526-9. doi: 10.1128/jcm.35.6.1526-1529.1997.
It is well known that Giardia lamblia and Cryptosporidium parvum can cause severe symptoms in humans, particularly those who are immunologically compromised. Immunoassay procedures offer both increased sensitivity and specificity compared to conventional staining methods. These reagents are also helpful when screening large numbers of patients, particularly in an outbreak situation or when screening patients with minimal symptoms. The data obtained by using 9 diagnostic kits were compared: direct fluorescent-antibody assay (DFA) kits (TechLab Giardia/Crypto IF kit, TechLab Crypto IF kit, and Meridian Merifluor Cryptosporidium/Giardia) and enzyme immunoassay (EIA) kits (Alexon ProSpecT Giardia EZ Microplate Assay, Alexon ProSpecT Cryptosporidium Microplate Assay, Cambridge Giardia lamblia Antigen Microwell ELISA, Meridian Premier Giardia lamblia, Meridian Premier Cryptosporidium, TechLab Giardia CELISA, Trend Giardia lamblia EIA). The test with the Meridian Merifluor Cryptosporidium/Giardia kit was used as the reference method. In various combinations, 60 specimens positive for Giardia, 60 specimens positive for Cryptosporidium, 40 specimens positive for a Giardia-Cryptosporidium mix, and 50 negative fecal specimens were tested. Different species (nine protozoa, three coccidia, one microsporidium, five nematodes, three cestodes, and one trematode) were included in the negative specimens. The sensitivity of EIA for Giardia ranged from 94% (Alexon) to 99% (Trend and Cambridge); the specificity was 100% with all EIA kits tested. The sensitivity of EIA for Cryptosporidium ranged from 98% (Alexon) to 99% (Meridian Premier); specificities were 100%. All DFA results were in agreement, with 100% sensitivity and specificity; however, the TechLab reagents resulted in fluorescence intensity that was generally one level below that seen with the reagents used in the reference method. In addition to sensitivity and specificity, factors such as cost, simplicity, ease of interpretation of results (color, intensity of fluorescence), equipment, available personnel, and number of tests ordered are also important considerations prior to kit selection.
众所周知,蓝氏贾第鞭毛虫和微小隐孢子虫可在人类中引发严重症状,尤其是免疫功能低下者。与传统染色方法相比,免疫测定程序具有更高的灵敏度和特异性。这些试剂在筛查大量患者时也很有帮助,特别是在爆发疫情的情况下或筛查症状轻微的患者时。对使用9种诊断试剂盒获得的数据进行了比较:直接荧光抗体检测(DFA)试剂盒(TechLab贾第虫/隐孢子虫免疫荧光试剂盒、TechLab隐孢子虫免疫荧光试剂盒和Meridian Merifluor隐孢子虫/贾第鞭毛虫试剂盒)和酶免疫测定(EIA)试剂盒(Alexon ProSpecT贾第虫酶联免疫吸附测定微孔板检测、Alexon ProSpecT隐孢子虫微孔板检测、剑桥蓝氏贾第鞭毛虫抗原微孔板酶联免疫吸附测定、Meridian Premier蓝氏贾第鞭毛虫、Meridian Premier隐孢子虫、TechLab贾第虫酶联免疫吸附测定、Trend蓝氏贾第鞭毛虫酶免疫测定)。以Meridian Merifluor隐孢子虫/贾第鞭毛虫试剂盒检测作为参考方法。对60份贾第虫阳性标本、60份隐孢子虫阳性标本、40份贾第虫-隐孢子虫混合阳性标本和50份粪便阴性标本进行了不同组合的检测。阴性标本中包含不同种类(9种原生动物、3种球虫、1种微孢子虫、5种线虫、3种绦虫和1种吸虫)。EIA检测贾第虫的灵敏度范围为94%(Alexon)至99%(Trend和剑桥);所有检测的EIA试剂盒特异性均为100%。EIA检测隐孢子虫的灵敏度范围为98%(Alexon)至99%(Meridian Premier);特异性均为100%。所有DFA结果一致,灵敏度和特异性均为100%;然而,TechLab试剂产生的荧光强度通常比参考方法中使用的试剂低一个级别。除了灵敏度和特异性外,在选择试剂盒之前,诸如操作简便性、结果解读的难易程度(颜色、荧光强度)、设备、可用人员以及检测订单数量等因素也是重要的考虑因素。