首页> 外文OA文献 >An Accurate Confirmation of Human Immunodeficiency Virus Type 1 (HIV-1) and 2 (HIV-2) Infections with a Dot blot assay Using Recombinant p24, gp41, gp120 and gp36 Antigens
【2h】

An Accurate Confirmation of Human Immunodeficiency Virus Type 1 (HIV-1) and 2 (HIV-2) Infections with a Dot blot assay Using Recombinant p24, gp41, gp120 and gp36 Antigens

机译:使用重组p24,gp41,gp120和gp36抗原的斑点印迹法准确确认1型人类免疫缺陷病毒(HIV-1)和2型(HIV-2)感染

摘要

An immunoblot assay using four recombinant proteins corresponding to human immunodeficiency virus type 1 (HIV-1) and type 2 (HIV-2) gene products was developed to confirm the presence of antibodies to HIV-1 and 2 in sera reactive in screening ELISAs. Serum samples for testing were obtained from healthy seronegative blood donors and from different categories of HIV-infected individuals (asymptomatic HIV-infected, and AIDS). A positive reaction was defined as reactivity against gag (p24) and at least one other env (either gp41 or gp120) HIV gene products; negative result was defined as no reaction with any antigen; and indeterminate result was defined as reactivity with gag (p24) or with env (gp41 or gp120) alone. None of the 180 serum samples from healthy seronegative blood donors gave a positive result, and only 4 of these samples (2.2%) gave indeterminate results. The recombinant HIV Dot blotting assay identified seropositive individuals with a high degree of accuracy; none of the 125 HIV-seropositive subjects had a negative test result. Reactivity with these antigens, demonstrated 100% sensitivity and specificity in distinguishing seronegative from seropositive sera. All seronegative and seropositive samples were tested both with the commercially available ELISA and by Western blot. The recombinant in-house HIV Dot blot assay accurately identified more seropositive and seronegative samples and had fewer indeterminate results than did commercial Western blot (as interpreted by CDC criteria).
机译:开发了一种免疫印迹测定法,使用四种重组蛋白分别对应人类1型(HIV-1)和2型(HIV-2)人类免疫缺陷病毒基因产物,以确认筛选ELISA中反应性血清中HIV-1和2抗体的存在。从健康的血清阴性献血者和不同类别的HIV感染者(无症状的HIV感染者和AIDS)获得血清进行测试。阳性反应定义为对gag(p24)和至少一种其他env(gp41或gp120)HIV基因产物有反应性。阴性结果定义为不与任何抗原反应;不确定的结果定义为与gag(p24)或与env(gp41或gp120)的反应性。来自健康血清阴性献血者的180个血清样品中没有一个给出阳性结果,而这些样品中只有4个(2.2%)给出不确定的结果。重组HIV Dot印迹法可高度准确地鉴定出血清反应阳性的个体。在125名HIV血清阳性患者中,没有一个检测结果阴性。与这些抗原的反应性在区分血清反应阳性和血清反应阳性血清方面显示出100%的敏感性和特异性。所有血清反应阴性和血清反应阳性的样品均使用市售ELISA和Western blot检测。与商业Western印迹法(由CDC标准解释)相比,重组的内部HIV Dot印迹法可准确鉴定出更多的血清反应阳性和血清阴性样品,并且不确定的结果更少。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号