Autoimmune myasthenia gravis (MG) is a neuromuscular disorder caused by autoantibodies directed against the acetylcholine receptor (AChR). Current symptomatic therapy is based on acetylcholinesterase (AChE) drugs. The available long-term current therapy includes steroids and other immunomodulatory agents. MG is associated with the production of a soluble, rare isoform of AChE, also referred as the "read-through" transcript (AChE-R). Monarsen (EN101) is a synthetic antisense compound directed against the AChE gene. Monarsen was administered in 16 patients with MG and 14 patients achieved a clinically signifcant response. The drug is now in a Phase II study. Further investigations are required to confrm its long-term effects. © 2013 Angelini et al, publisher and licensee Dove Medical Press Ltd.
New treatments for myasthenia: A focus on antisense oligonucleotides
Angelini C.
Conceptualization
;
2013
Abstract
Autoimmune myasthenia gravis (MG) is a neuromuscular disorder caused by autoantibodies directed against the acetylcholine receptor (AChR). Current symptomatic therapy is based on acetylcholinesterase (AChE) drugs. The available long-term current therapy includes steroids and other immunomodulatory agents. MG is associated with the production of a soluble, rare isoform of AChE, also referred as the "read-through" transcript (AChE-R). Monarsen (EN101) is a synthetic antisense compound directed against the AChE gene. Monarsen was administered in 16 patients with MG and 14 patients achieved a clinically signifcant response. The drug is now in a Phase II study. Further investigations are required to confrm its long-term effects. © 2013 Angelini et al, publisher and licensee Dove Medical Press Ltd.| File | Dimensione | Formato | |
|---|---|---|---|
|
DDDT-25716-future-prospects-for-the-treatment-of-myasthenia-gravis--a-f_010913.pdf
accesso aperto
Tipologia:
Published (Publisher's Version of Record)
Licenza:
Creative commons
Dimensione
329.83 kB
Formato
Adobe PDF
|
329.83 kB | Adobe PDF | Visualizza/Apri |
Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.




