Crouvezier Nicolas, Marie Anne-Céline, Moumné Lara
Inserm Transfert, 7 rue Watt, 75013 Paris, France.
Med Sci (Paris). 2023 Feb;39(2):111-118. doi: 10.1051/medsci/2023005. Epub 2023 Feb 17.
Oligonucleotides are small nucleic acids capable of interacting with DNA or RNA to modulate gene expression. Widely used by researchers as research tools to modulate the expression of the genes they seek to decipher the function, oligonucleotides can also serve as therapeutic agents to regulate targets of interest. After the first marketing authorisation of an oligonucleotide therapeutics in 1998, the field met little clinical success until 2016 when Spinraza® became the first drug authorized for spinal muscular atrophy. This compound became in the following years the first "blockbuster" among this class of molecules, validating the commercial potential of oligonucleotide drugs. Since then, about ten other oligonucleotides hit the market and a broad pipeline is currently in late clinical development. Through our article, we describe therapeutic oligonucleotides, their modes of action and their patentability.
寡核苷酸是能够与DNA或RNA相互作用以调节基因表达的小核酸。研究人员广泛将其用作研究工具来调节他们试图解读功能的基因的表达,寡核苷酸也可以作为治疗剂来调节感兴趣的靶点。1998年寡核苷酸疗法首次获得上市许可后,该领域在临床方面几乎没有取得成功,直到2016年Spinraza®成为首个被批准用于治疗脊髓性肌萎缩症的药物。在接下来的几年里,这种化合物成为了这类分子中的首个“重磅炸弹”药物,证实了寡核苷酸药物的商业潜力。从那时起,又有大约十种其他寡核苷酸上市,目前还有一大批处于临床后期开发阶段。通过我们的文章,我们描述了治疗性寡核苷酸、它们的作用方式以及它们的可专利性。