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Gene patents and personalized medicine - what lies ahead?

机译:基因专利和个性化药物-未来将是什么?

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摘要

Gene patents have generally not impeded biomedical research, but some problems that arise in genetic diagnostics can be attributed to exclusively licensed gene patents. Gene patents for therapeutics have often been litigated but have received surprisingly little public outcry. In stark contrast, genetic diagnostics have been highly controversial but rarely litigated: no case has gone to trial and there is little case law to guide policy. Most recently the Secretary's Advisory Committee for Genetics Health and Society (SACGHS) released a draft report examining how patenting and licensing affect access to clinical genetic testing in the US. The SACGHS reported that patents neither greatly hindered nor facilitated patient access to genetic testing; both the harms and the benefits of patents on genetic diagnostics have been exaggerated. Problems do occur when patents are exclusively licensed to a single provider and no alternative is available. Courts have been changing the thresholds for what can be patented, and how strongly patents can be enforced. Technologies for sequencing, genotyping and gene expression profiling promise to guide clinical decisions in managing common chronic diseases and infectious diseases, and will likely be an integral part of personalized medicine. Developing such genomic tests may require mapping a complex intellectual property landscape and cutting through thickets of patented DNA sequences and related methods. Our preliminary studies have found patent claims that, if strictly enforced, might block the use of multi-gene tests or full-genome sequence data. Yet new technologies promise to reduce the costs of complete genomic sequencing to prices that are comparable to current genetic tests for a single condition. Courts, companies, and policy makers seem unlikely to allow intellectual property to obstruct such technological advance, but prudent policy will depend on careful analysis and foresight. The SACGHS report signals that the US government is paying attention, and increases the odds that policy will foster socially beneficial uses of genetic testing while preserving intellectual property incentives and mitigating the problems that arise from legal monopolies.
机译:基因专利通常不会阻碍生物医学研究,但是基因诊断中出现的一些问题可以归因于独家许可的基因专利。用于治疗剂的基因专利通常已提起诉讼,但令人惊讶的是,很少有人对此提出强烈抗议。与之形成鲜明对比的是,基因诊断一直备受争议,但很少提起诉讼:没有案件要审理,几乎没有判例法可以指导政策。最近,秘书的遗传健康与社会咨询委员会(SACGHS)发布了一份报告草稿,研究了专利和许可如何影响美国临床基因检测的获取。 SACGHS报告说,专利既没有极大地阻碍也没有促进患者进行基因检测。基因诊断专利的危害和利益都被夸大了。当专利被独家授权给单个提供商并且没有其他替代方法时,确实会出现问题。法院一直在改变可以申请专利的门槛,以及可以强制执行专利的门槛。测序,基因分型和基因表达谱分析技术有望指导管理常见慢性病和传染病的临床决策,并且可能将成为个性化医学不可或缺的一部分。开发此类基因组测试可能需要绘制复杂的知识产权图景,并突破获得专利的DNA序列和相关方法的丛林。我们的初步研究发现,如果严格执行专利申请,可能会阻止使用多基因检测或全基因组序列数据。然而,新技术有望将完整基因组测序的成本降低到与当前针对单个条件的基因测试相当的价格。法院,公司和政策制定者似乎不太可能允许知识产权阻碍这种技术进步,但审慎的政策将取决于认真的分析和远见。 SACGHS报告表明美国政府正在关注,并增加了政策将促进基因检测对社会有益的利用,同时保留知识产权激励措施并减轻由法律垄断引起的问题的可能性。

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