Manavi K, Young H, McMillan A
Department of Genitourinary Medicine, Whittall Street Clinic, Whittall Street, Birmingham B4 6DH, UK.
Int J STD AIDS. 2006 Nov;17(11):768-71. doi: 10.1258/095646206778691185.
Our aim was to determine the sensitivity of the Murex ICE enzyme immunoassay (EIA) as a screening test for early syphilis and to determine how many additional cases of infection were detected by performing additional tests when requested on clinical grounds. This was an observational study on consecutive patients diagnosed with syphilis in the Department of Genitourinary Medicine, Edinburgh between January 1st 2004 and April 1st 2005. Additional tests were performed on sera that gave a positive or equivocal EIA on screening as well as by clinical request on sera from contacts of syphilis, and those with clinical signs of syphilis. Additional tests included a Venereal Diseases Research Laboratory (VDRL) carbon antigen test, a Treponema pallidum particle agglutination (TPPA) test, INNO-LIA line immunoblot assay, and an EIA specific for anti-treponemal IgM.A total of 105 patients were diagnosed with syphilis: primary (50), secondary (26), early latent (8), and of unknown duration (21). The TPPA was the most sensitive test in primary syphilis and had a sensitivity of 96% (48/50), which was significantly higher (P <0.05) than the sensitivity of 84% (42/50) for the screening EIA: seven of the EIA negatives were detected by EIA-IgM, six by TPPA, five by immunoblot, and two by VDRL. EIA-IgM was negative in six primaries; all were positive by TPPA and immunoblot. We conclude that, in order to maximize the serological detection of primary syphilis a specific EIA-IgM test and a TPPA test should be performed whenever there is a clinical suspicion of primary infection. This is particularly important when an EIA such as Murex ICE is used as a single screening test as it is less sensitive than the TPPA in primary infection.
我们的目的是确定Murex ICE酶免疫测定法(EIA)作为早期梅毒筛查试验的敏感性,并确定基于临床理由要求进行额外检测时能检测出多少额外的感染病例。这是一项对2004年1月1日至2005年4月1日期间在爱丁堡泌尿生殖医学部连续诊断为梅毒的患者进行的观察性研究。对筛查时EIA呈阳性或疑似阳性的血清以及应临床要求对梅毒接触者和有梅毒临床体征者的血清进行额外检测。额外检测包括性病研究实验室(VDRL)碳抗原试验、梅毒螺旋体颗粒凝集(TPPA)试验、INNO-LIA线性免疫印迹试验以及抗梅毒螺旋体IgM特异性EIA。共有105例患者被诊断为梅毒:一期(50例)、二期(26例)、早期潜伏(8例)和病程不明(21例)。TPPA在一期梅毒中是最敏感的检测方法,敏感性为96%(48/50),显著高于筛查EIA的84%(42/50)(P<0.05):EIA阴性的7例通过EIA-IgM检测出,6例通过TPPA检测出,5例通过免疫印迹检测出,2例通过VDRL检测出。6例一期梅毒患者EIA-IgM为阴性;所有患者TPPA和免疫印迹均为阳性。我们得出结论,为了最大限度地通过血清学检测出一期梅毒,每当临床怀疑有原发感染时,应进行特异性EIA-IgM检测和TPPA检测。当使用如Murex ICE这样的EIA作为单一筛查试验时,这一点尤为重要,因为它在原发感染中比TPPA敏感性低。