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Cytokine biomarkers as biomarkers predictive of the clinical response for glatiramer acetate

机译:细胞因子生物标志物可预测醋酸格拉替雷的临床反应

摘要

A procedure for predicting the degree of clinical response to treatment with glatiramer acetate in a human subject suffering from multiple sclerosis or a single clinical attack consistent with multiple sclerosis, the method comprising assessing the concentration of IL-17 in the supernatant of the CMSP from of the subject's blood, and identify the human subject as a patient responding to glatiramer acetate based on the concentration of IL-17, this subject being identified as a patient responding to glatiramer acetate through the steps comprising, (i) purify the CMSP from the subject's blood and then cryopreserve the CMSP; (ii) thaw and then cultivate cryopreserved CMSPs overnight in culture medium enriched with 5% human serum; (iii) stimulate 40,000 of said CMSPs grown with 1 mg / ml of PMA and 5 mg / ml of ionomycin in a final volume of 200 microliters for 6 hours; and (v) identify the human subject as a patient responding to glatiramer acetate if the IL-17 concentration of the CMSP supernatant after step (iii) is greater than or equal to 120 pg / ml,
机译:在患有多发性硬化或与多发性硬化一致的单次临床发作的人类受试者中,预测用醋酸格拉替雷治疗的临床反应程度的方法,该方法包括:从小鼠中评估CMSP上清液中IL-17的浓度。受试者的血液,并根据IL-17的浓度将人类受试者确定为对醋酸格拉替雷有反应的患者,通过以下步骤将受试者确定为对醋酸格拉替雷有反应的患者:(i)从受试者的血浆中纯化CMSP血液然后冷冻保存CMSP; (ii)解冻,然后在富含5%人血清的培养基中过夜培养冷冻保存的CMSP; (iii)在200微升的最终体积中刺激40,000个所述CMSP与1mg / ml PMA和5mg / ml离子霉素一起生长6小时; (v)如果步骤(iii)之后CMSP上清液的IL-17浓度大于或等于120 pg / ml,则将人类受试者识别为对醋酸格拉替雷有反应的患者,

著录项

  • 公开/公告号ES2602977T3

    专利类型

  • 公开/公告日2017-02-23

    原文格式PDF

  • 申请/专利权人 TEVA PHARMACEUTICAL INDUSTRIES LTD.;

    申请/专利号ES20110833199T

  • 发明设计人 KASPER LLOYD;SMITH JACQUELINE;

    申请日2011-10-10

  • 分类号G01N33/68;A61K9;A61K31/785;A61K38/07;C07K14/52;

  • 国家 ES

  • 入库时间 2022-08-21 13:35:26

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