Rogers R, Windust A, Gregory J
Haematology Laboratory, Royal Berkshire Hospital, Reading, Berkshire RG1 5AN, United Kingdom.
J Clin Microbiol. 1999 Jan;37(1):95-8. doi: 10.1128/JCM.37.1.95-98.1999.
A new, dried antigen-coated latex preparation for the demonstration of infectious mononucleosis (IM) heterophile antibody (Dryspot IM kit; Oxoid, Ltd., Basingstoke, Hampshire, United Kingdom) was compared with the IM kit (a liquid latex reagent from the same source), an immunoassay (ImmunoCard Mono; Meridian Diagnostics), and an absorption test (Monospot; Meridian Diagnostics). The latter was used as a standard for initial statistical comparisons. Discrepancies were resolved by using Epstein-Barr virus serology. Of the 328 routine samples tested, 77 were positive and 222 were negative by all IM heterophile antibody-based kits. Twenty-nine samples gave discrepant results. Following resolution of discrepant results, the sensitivity and specificity values for the IM Dryspot kit were 87.0 and 98.7%, those for the Oxoid liquid latex IM kit were 83.0 and 99.6%, and those for the ImmunoCard Mono immunoassay were 85.0 and 100.0%, respectively. The evaluation shows that the Dryspot kit, which is uniquely straightforward to use and may be stored at room temperature, is comparable in performance to other rapid heterophile tests for the confirmation of IM.
一种用于检测传染性单核细胞增多症(IM)嗜异性抗体的新型干燥抗原包被乳胶制剂(Dryspot IM试剂盒;Oxoid有限公司,英国汉普郡贝辛斯托克),与IM试剂盒(来自同一来源的液体乳胶试剂)、免疫测定法(ImmunoCard Mono;Meridian诊断公司)和吸收试验(Monospot;Meridian诊断公司)进行了比较。后者用作初始统计比较的标准。通过使用爱泼斯坦-巴尔病毒血清学解决了差异。在328份常规检测样本中,所有基于IM嗜异性抗体的试剂盒检测结果显示,77份为阳性,222份为阴性。29份样本结果存在差异。在解决差异结果后,IM Dryspot试剂盒的灵敏度和特异性值分别为87.0%和98.7%,Oxoid液体乳胶IM试剂盒为83.0%和99.6%,ImmunoCard Mono免疫测定法为85.0%和100.0%。评估表明,Dryspot试剂盒使用极其简便,可在室温下储存,在性能上与其他用于确诊IM的快速嗜异性检测方法相当。