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基因专利和授权实践对听力损失基因检测可及性的影响。

Impact of gene patents and licensing practices on access to genetic testing for hearing loss.

机构信息

Center for Public Genomics, Center for Genome Ethics, Law and Policy, Institute for Genome Sciences and Policy, Duke University, Durham, NC 27708, USA.

出版信息

Genet Med. 2010 Apr;12(4 Suppl):S171-93. doi: 10.1097/GIM.0b013e3181d7b053.

Abstract

Genetic testing for heritable hearing loss involves a mix of patented and unpatented genes, mutations and testing methods. More than half of all hearing loss is linked to inherited mutations, and five genes are most commonly tested for in the United States. There are no patents on three of these genes, but Athena Diagnostics holds exclusive licenses to test for a common mutation in the GJB2 gene associated with about 50% of all cases as well as mutations in the MTRNR1 gene. This fragmented intellectual property landscape made hearing loss a useful case study to assess whether patent rights in genetic testing can proliferate or overlap, and whether it is possible to gather the rights necessary to perform testing. Testing for hearing loss is widely available, primarily from academic medical centers. Based on literature reviews and interviews with researchers, research on the genetics of hearing loss has generally not been impeded by patents. There is no consistent evidence of a premium in testing prices attributable to patent status. Athena Diagnostics has, however, used its intellectual property to discourage other providers from offering some tests. There is no definitive answer about the suitability of current patenting and licensing of commonly tested genes because of continuing legal uncertainty about the extent of enforcement of patent rights. Clinicians have also expressed concerns that multiplex tests will be difficult to develop because of overlapping intellectual property and conflict with Athena's sole provider business model.

摘要

遗传性听力损失的基因检测涉及专利和非专利基因、突变和检测方法的混合。超过一半的听力损失与遗传突变有关,在美国最常检测的是五个基因。其中三个基因没有专利,但雅典娜诊断公司拥有独家许可,可以检测与 50%所有病例相关的 GJB2 基因常见突变以及 MTRNR1 基因突变。这种零散的知识产权格局使得听力损失成为一个有用的案例研究,可以评估基因检测中的专利权利是否会扩散或重叠,以及是否有可能收集进行检测所需的权利。听力损失检测广泛可用,主要来自学术医疗中心。基于文献综述和对研究人员的采访,听力损失遗传学研究一般没有受到专利的阻碍。没有一致的证据表明,测试价格因专利状况而出现溢价。然而,雅典娜诊断公司利用其知识产权阻止其他供应商提供某些测试。由于对专利权利执行范围的法律不确定性持续存在,目前对常见检测基因的专利和许可的适用性尚无明确答案。临床医生还表示担心,由于知识产权重叠以及与雅典娜唯一供应商商业模式的冲突,多重检测将难以开发。

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