IP Library Granted Patent US 10,874,637
Granted Patent B2
US 10,874,637 · App. 16/471,307 · Granted Dec 29, 2020

Methods and pharmaceutical compositions for the treatment of neurodegeneration with brain iron accumulation

Inventors: Anne Agnès Rötig (Paris, FR); Anthony Drecourt (Paris, FR)
Assignees: INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MÉDICALE); UNIVERSITÉ PARIS DESCARTES; FONDATION IMAGING; ASSISTANCE PUBLIQUE-HÔPITAUX DE PARIS (APHP)
A61K31/357A61P25/28
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Quick Facts
Patent No.
US 10,874,637
App. No.
16/471,307
Granted
Dec 29, 2020
Kind
B2
Abstract

The present invention relates to methods and pharmaceutical compositions for the treatment of neurodegeneration in with brain iron accumulation (NBIA). Studying two novel genes, namely, CRAT encoding the carnitine acetyltransferase and REPS1 involved in endocytosis and vesicle transport, and a series of known NBIA genes, the inventors reported on iron overload related to increased levels and abnormal recycling of transferrin receptor as a common feature in NBIA. They ascribe this anomaly, at least in part, to impaired palmitoylation of the receptor as a common consequence of the various disease causing mutations. Finally, the inventors show that Artesunate improved TfR1 palmitoylation in NBIA fibroblasts. In particular, the present invention relates to a method of treating neurodegeneration with brain iron accumulation in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a drug increasing TfR1 palmitoylation.

Claims (4)

1. A method of treating neurodegeneration with brain iron accumulation (NBIA) in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a drug increasing transferrin receptor 1 (TfR1) palmitoylation, wherein the drug is selected from the group consisting of artesunate, a prodrug of artesunate and artemisinin.

2. The method of claim 1 wherein the NBIA results from a disease gene selected from PANK2, PLA2G6, COASY, FA2H, ATP13A2, C2orf37, WDR45, C19ORFf12, CP, FTL, GTPBP2, CRAT and REPS1.

3. The method of claim 1 wherein the NBIA is pantothenic kinase-associated neurodegeneration, infantile neuroaxonal dystrophy, atypical neuroaxonal dystrophy, mitochondrial-membrane protein-associated neurodegeneration, beta-propeller protein-associated neurodegeneration, aceruloplasminemia, fatty acid hydroxylase-associated neurodegeneration, neuroferritinopathy, Woodhouse-Sakati syndrome, or coasy protein-associated neurodegeneration.

4. A method of treating neurodegeneration with brain iron accumulation (NBIA) in a subject in need thereof comprising administering to the subject a therapeutically effective amount of artesunate, wherein said therapeutically effective amount is sufficient to increase transferrin receptor 1 (TfR1) palmitoylation in cells of the subject.

Assignments (3)
CHANGE OF NAME Recorded May 12, 2022
From: UNIVERSITE DE PARIS
To: UNIVERSITÉ PARIS CITÉ
Reel/Frame 059988/0388 →
MERGER Recorded May 12, 2022
From: UNIVERSITE PARIS DESCARTES
To: UNIVERSITE DE PARIS
Reel/Frame 060044/0856 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2020
From: RÖTIG, ANNE AGNÈS; DRECOURT, ANTHONY
To: INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE); UNIVERSITÉ PARIS DESCARTES; FONDATION IMAGINE; ASSISTANCE PUBLIQUE-HÔPITAUX DE PARIS (APHP)
Reel/Frame 052015/0354 →