首页> 外国专利> SOLUBLE LEISHMANIA ANTIGEN SPECIFIC WHOLE BLOOD ASSAY AS A MARKER OF ASYMPTOMATIC INFECTION AND DISEASE STATUS IN HUMAN VISCERAL LEISHMANIASIS

SOLUBLE LEISHMANIA ANTIGEN SPECIFIC WHOLE BLOOD ASSAY AS A MARKER OF ASYMPTOMATIC INFECTION AND DISEASE STATUS IN HUMAN VISCERAL LEISHMANIASIS

机译:可溶性利什曼原虫抗原特异性全血检测是人类内脏利什曼病无症状感染和疾病状态的标志

摘要

In regions endemic for Visceral leishmaniasis (VL), asymptomatic infection is common and only a small proportion of persons infected with L.donovani develop clinical VL, characterized by febrile splenomegaly and pancytopenia. To detect infection in healthy persons, the Montenegro test or Leishmania skin test (LST) is used along with serological markers. Unfortunately, both tests have many drawbacks: their sensivity and specificity for infection are not clearly established and for LST, lack of GMP grade L.donovani antigen, intradermal administration and reading after 48 hrs. make it very tedious procedure. The present invention provides the compounds and methods of soluble leishmania antigen specific whole blood assay for the detection of IFN-γ production by L. donovani infected, asymptomatic individuals, and for detection of IL-10 secretion as the signature cytokine distinguishing active VL from cured or asymptomatic cases control for monitoring of ongoing transmission in endemic area.
机译:在内脏利什曼病(VL)流行地区,无症状感染很常见,只有一小部分感染L.donovani的人会发展为临床VL,其特征是发热性脾肿大和全血细胞减少。为了检测健康人的感染,将黑山测试或利什曼原虫皮肤测试(LST)与血清学标记物一起使用。不幸的是,这两种测试均具有许多缺点:对感染的敏感性和特异性尚不清楚,对LST,缺乏GMP等级的L.donovani抗原,皮内给药和48小时后读数也没有。使程序变得非常乏味。本发明提供了可溶的利什曼原虫抗原特异性全血测定的化合物和方法,用于检测被多巴氏乳杆菌感染的无症状个体产生的IFN-γ,以及检测IL-10分泌作为区分活性VL和治愈VL的标志性细胞因子。或无症状病例控制,以监测流行地区的持续传播。

著录项

  • 公开/公告号IN2011DE03379A

    专利类型

  • 公开/公告日2012-04-20

    原文格式PDF

  • 申请/专利权人

    申请/专利号IN3379/DEL/2011

  • 发明设计人 OM PRAKASH SINGH;SHAYAM SUNDER;

    申请日2011-11-25

  • 分类号

  • 国家 IN

  • 入库时间 2022-08-21 17:24:11

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