Thakar Y S, Chande C, Mahalley A D, Saoji A M
Department of Microbiology, Government Medical College, Nagpur.
Indian J Pathol Microbiol. 1996 Apr;39(2):135-8.
A total of 1074 sera obtained from clinically suspected cases of Syphilis and various risk groups were screened for antitreponemal antibodies by Treponema pallidum Haemagglutination (TPHA) test and cardiolipin antibodies by the Venereal Disease Research Laboratory (VDRL) tests. The TPHA test was positive in 291 (27.09) per cent. The TPHA was positive in 53.31 per cent (161 out of 302) patients of primary syphilis, 54.17 per cent (26 out of 48) of secondary, 32.76 per cent (19 out of 58) of tertiary syphilis, 17.12 per cent (19 out of 111) of other Sexually Transmitted Disease (STD) patients, 25.32 per cent (60 out of 237) pregnant women and 1.89 per cent (6 out of 318) healthy individuals. TPHA was found to be superior to VDRL test in all the study groups. Almost a total agreement was seen between the TPHA test and VDRL test with a titre of 1 in 16 & above; while in as many as 32.39 per cent sera with VDRL titre of 1 in 8 TPHA was negative indicating that the VDRL titres above 1 in 8 should be considered as true reactives to minimize the biological false positive reactions.
通过梅毒螺旋体血凝试验(TPHA)对1074份来自临床疑似梅毒病例及各类风险人群的血清进行抗梅毒螺旋体抗体筛查,并通过性病研究实验室试验(VDRL)检测心磷脂抗体。TPHA试验阳性率为291例(27.09%)。一期梅毒患者中TPHA阳性率为53.31%(302例中的161例),二期为54.17%(48例中的26例),三期为32.76%(58例中的19例),其他性传播疾病(STD)患者为17.12%(111例中的19例),孕妇为25.32%(237例中的60例),健康个体为1.89%(318例中的6例)。在所有研究组中,TPHA被发现优于VDRL试验。TPHA试验与VDRL试验在滴度为1:16及以上时几乎完全一致;而在VDRL滴度为1:8的血清中,多达32.39%的血清TPHA为阴性,这表明VDRL滴度高于1:8时应被视为真正的反应性结果,以尽量减少生物学假阳性反应。