新疗法的未来是怎样的

K. Bork
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引用次数: 0

摘要

目前正在研究一些新的潜在治疗遗传性血管性水肿(HAE)的方法。它们包括接触系统的新抑制剂,如ecallantide,一种缓激肽抑制剂,Icatibant,一种缓激肽受体B2拮抗剂,以及在转基因家兔乳中分泌的重组C1-INH。有关这些最先进治疗方法的数据的发表可能是HAE治疗新治疗进展的开始,并有望减少这种疾病所带来的负担。
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Quel avenir pour les nouvelles thérapeutiques ?

A certain number of new potential therapies for hereditary angioedema (HAE) are currently being studied. They include new inhibitors of the contact system, such as ecallantide, a kallikrein inhibitor, Icatibant, a bradykinin receptor B2 antagonist, as well as a recombinant C1-INH secreted in the milk of transgenic rabbits. Publication of the data concerning these state-of-the-art therapies could be the beginning of new therapeutic advances in the treatment of HAE and, hopefully, lead to reduction in the burden that this condition represents.

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Editorial Board Page tournée et nouveaux rendez-vous L’enseignement de l’allergologie pendant les études médicales en France Toux chronique de l’adulte et reflux gastro-œsophagien Les frontières du bilan allergologique en allergo-anesthésie
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