Castro Arnold R, Kikkert Susan E, Fears Martha B, Pope Victoria
Syphilis and Chlamydia Branch, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
Clin Diagn Lab Immunol. 2002 Nov;9(6):1376-8. doi: 10.1128/cdli.9.6.1376-1378.2002.
Syphilitic plasma can be salvaged from discarded blood donations and converted to serum by defibrination. Sixty-nine units of plasma were treated with a stock solution of 100 U of thrombin per ml in 1 M calcium chloride and then with a 10% (wt/vol) solution of kaolin. Fibrinogen concentrations detected in initial plasma samples ranged from 94 to 4970 mg/liter (mean, 2532 mg/liter) for samples that were reactive by the rapid plasma reagin circle card test (RPR) and from 314 to 2742 mg/liter (mean 1528 mg/liter) for samples that were not reactive by the RPR. The treated samples showed no measurable fibrinogen remaining after the defibrination process. In the nontreponemal RPR for syphilis, 86% of the treated plasma samples retained the same endpoint titer as that of the initial plasma sample. When the Treponema pallidum passive-particle-agglutination test was used, 98% retained the same reactivity. In the Captia Syphilis-G enzyme immunoassay, 89% of the treated samples demonstrated no change in reactivity index, and in the fluorescent treponemal antibody absorption test, 96% showed no reduction in fluorescence. Human sera containing antibodies to syphilis are used at the Centers for Disease Control and Prevention for the preparation of reference controls or as samples for proficiency testing. Finding reactive sera is becoming more difficult due to the general decline of syphilis cases in the United States. The decreasing availability of these sera can be alleviated by salvaging plasma and converting it to serum.
梅毒血浆可从废弃的献血中回收,并通过去纤维蛋白作用转化为血清。69单位血浆先用每毫升含100单位凝血酶的储备液在1M氯化钙中处理,然后用10%(重量/体积)高岭土溶液处理。快速血浆反应素环状卡片试验(RPR)呈反应性的样本,初始血浆样本中检测到的纤维蛋白原浓度范围为94至4970毫克/升(平均2532毫克/升);RPR无反应性的样本,纤维蛋白原浓度范围为314至2742毫克/升(平均1528毫克/升)。处理后的样本在去纤维蛋白过程后未检测到残留的可测量纤维蛋白原。在梅毒的非梅毒螺旋体RPR试验中,86%的处理后血浆样本保持与初始血浆样本相同的终点滴度。当使用梅毒螺旋体颗粒凝集试验时,98%的样本保持相同的反应性。在Captia梅毒-G酶免疫测定中,89%的处理后样本反应性指数无变化;在荧光螺旋体抗体吸收试验中,96%的样本荧光未降低。美国疾病控制与预防中心使用含梅毒抗体的人血清制备参考对照或作为能力验证的样本。由于美国梅毒病例总体下降,寻找有反应性的血清变得更加困难。通过回收血浆并将其转化为血清,可以缓解这些血清供应减少的问题。