首页> 外国专利> METHOD OF EVALUATING THE EFFECTIVENESS OF ANTI-TUBERCULOSIS THERAPY IN PATIENTS WITH GENITAL TUBERCULOSIS

METHOD OF EVALUATING THE EFFECTIVENESS OF ANTI-TUBERCULOSIS THERAPY IN PATIENTS WITH GENITAL TUBERCULOSIS

机译:评估遗传性结核病患者抗结核治疗效果的方法

摘要

FIELD: medicine.;SUBSTANCE: invention relates to medicine and is a method of evaluating the effectiveness of therapy of genital tuberculosis comprising control Immunoassays, characterized in that at the end of the initial phase of therapy is carried out 1st control, which comprises determining the stimulation index of interferon-gamma (IFN-γ) with purified tuberculin (PPD-L), the definition of the levels of specific immunoglobulins (IgA, IgM) for mycobacterium tuberculosis (MBT) by enzyme-linked immunosorbent assay (ELISA), and the 2nd control is carried out through the 6-11 months after the end of the main course of therapy, In the case when a stimulation index IFNγ with PPD-L at the end of the intensive phase of TB treatment was higher than 7, 8 - only IFNγ with PPD-A, if the optical density IgM to MBT has a 0.600 - only IgM to MBT, when the optical density at MBT to IgA was more than 0.450 - control is performed only to IgA; while the results of controlled studies recommend an extension or correction, or the end of therapy.;EFFECT: invention provides a more accurate assessment of TB therapy.;1 cl, 2 ex, 1 tbl
机译:技术领域本发明涉及医学,并且是一种评价生殖器结核治疗效果的方法,包括对照免疫测定法,其特征在于在治疗的初始阶段结束时进行 Sup> 对照,其中包括用纯化的结核菌素(PPD-L)确定干扰素-γ(IFN-γ)的刺激指数,酶对结核分枝杆菌(MBT)特异性免疫球蛋白(IgA,IgM)水平的定义联免疫吸附试验(ELISA),并且在治疗的主要过程结束后的6-11个月内进行第二次 对照,当PPD-L刺激指数为IFNγ时在结核病强化治疗期结束时,如果PPD-A的光密度IgM对MBT的光密度为0.600-仅MBg对IgA的IgM,则在PPD-A高于7、8 –仅IFNγ的情况下大于0.450-仅对IgA进行控制;对照研究的结果建议延长治疗或纠正治疗或结束治疗。效果:本发明对结核病治疗提供了更准确的评估。1cl,2 ex,1 tbl

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