首页> 外国专利> Methods of diagnosing clinical substypes of crohn's disease with characteristic responsiveness to anti-th1 cytokine therapy and a kit for diagnosing the same

Methods of diagnosing clinical substypes of crohn's disease with characteristic responsiveness to anti-th1 cytokine therapy and a kit for diagnosing the same

机译:诊断对th1细胞因子疗法具有特征性反应的克罗恩病临床亚型的方法和诊断该试剂盒的试剂盒

摘要

The present invention provides methods based on serological and genetic markers for diagnosing clinical subtypes of Crohn's disease (CD) having characteristic responsiveness to anti-Th1 cytokine therapy. In the methods of the invention, the presence of perinuclear anti-neutrophil antibody (pANCA), the presence of the TNFa10b4c1d3e3 haplotype or the presence of TNFa11b4c1d3e3 haplotype each is independently diagnostic of a clinical subtype of CD having an inferior clinical response to anti-Th1 cytokine therapy. In addition, the presence of the homozygous TNF-β 1111 haplotype involving the TNFc, aa13L, aa26 and NcoI loci is independently diagnostic of a clinical subtype of CD having an inferior clinical response to anti-Th1 cytokine therapy. The presence of speckling anti-pan polymorphonuclear antibody (SAPPA) is diagnostic of a clinical subtype of CD having a superior clinical response to anti-Th1 cytokine therapy.
机译:本发明提供了基于血清学和遗传标记的方法,用于诊断对抗Th1细胞因子疗法具有特征性响应的克罗恩氏病(CD)的临床亚型。在本发明的方法中,核周抗中性粒细胞抗体(pANCA)的存在,TNFa10b4c1d3e3单倍型的存在或TNFa11b4c1d3e3单倍型的存在各自独立地诊断了对抗Th1的临床反应较差的CD的临床亚型。细胞因子治疗。另外,涉及TNFc,aa13L,aa26和NcoI基因座的纯合TNF-β1111单倍型的存在独立地诊断了对抗Th1细胞因子疗法的临床反应较差的CD的临床亚型。有斑点的抗泛多形核抗体(SAPPA)的存在可诊断出CD的临床亚型,该CD对抗Th1型细胞因子疗法具有优异的临床反应。

著录项

  • 公开/公告号IL132285D0

    专利类型

  • 公开/公告日2001-03-19

    原文格式PDF

  • 申请/专利号IL19980132285

  • 发明设计人

    申请日1998-04-08

  • 分类号7G01NA;

  • 国家 IL

  • 入库时间 2022-08-22 01:24:59

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