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AGENTS FOR USE IN THE THERAPEUTIC OR PROPHYLACTIC TREATMENT OF MYOPIA OR HYPEROPIA

机译:用于弱视或矫正的治疗或预防性治疗的代理商

摘要

The present invention relates to agents for use in the prophylactic or therapeutic treatment of myopia in a subject, wherein said agents are capable of decreasing epidermal growth factor receptor (EGFR) signaling and/or signaling of another receptor susceptible for amphiregulin in a subject in a direct or indirect manner. The present invention further relates to agents for use in the prophylactic or therapeutic treatment of hyperopia in a subject, wherein said agents are capable of increasing epidermal growth factor receptor (EGFR) signaling and/or signaling of another receptor susceptible for amphiregulin in a subject. Furthermore, the present invention relates to methods for the diagnosis of myopia or hyperopia in a subject, comprising the steps of (a) providing a biological sample from the subject; (b) determining the amphiregulin level in said sample; (c) comparing the level determined in step (b) to the amphiregulin levels found in emmetropic jects or subjects going to be emmetropic; and (d) determining that the subject has myopia or is predisposed for the development of myopia in case the level determined in step (b) is higher than the amphiregulin levels found in emmetropic subjects or subjects going to be emmetropic; and determining that the subject has hyperopia or is predisposed for the development of hyperopia in case the level determined in step (b) is lower than the amphiregulin levels found in emmetropic subjects or subjects going to be emmetropic. Finally, the present invention relates to a method for identifying agents which associate with amphiregulin or fragments or variants thereof.
机译:本发明涉及用于在受试者中预防或治疗近视的药剂,其中所述药剂能够在受试者中降低表皮生长因子受体(EGFR)信号传导和/或在受试者中对双调蛋白敏感的另一种受体的信号传导。直接或间接方式。本发明进一步涉及用于受试者的远视眼的预防或治疗的药剂,其中所述药剂能够增加表皮生长因子受体(EGFR)信号传导和/或受试者中对双调蛋白敏感的另一种受体的信号传导。此外,本发明涉及在受试者中诊断近视或远视的方法,其包括以下步骤:(a)从受试者提供生物样品; (b)确定所述样品中的双调蛋白水平; (c)将步骤(b)中确定的水平与正视性注射液或正视性受试者中的双调蛋白水平进行比较; (d)如果步骤(b)中确定的水平高于正视受试者或正视受试者中的双调蛋白水平,则确定该受试者患有近视眼或易患近视;并且在步骤(b)中确定的水平低于正视受试者或正视受试者中发现的双调蛋白水平的情况下,确定该受试者患有远视或易患远视。最后,本发明涉及一种鉴定与双调蛋白或其片段或变体相关的试剂的方法。

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