Changing Times for CLN2 Disease: The Era of Enzyme Replacement Therapy

التفاصيل البيبلوغرافية
العنوان: Changing Times for CLN2 Disease: The Era of Enzyme Replacement Therapy
المؤلفون: Specchio, Nicola, Pietrafusa, Nicola, Trivisano, Marina
المصدر: Therapeutics and Clinical Risk Management
بيانات النشر: Dove, 2020.
سنة النشر: 2020
مصطلحات موضوعية: late infantile, cerliponase alfa, Review, neuronal ceroid lipofuscinosis type 2, TPP1, seizures
الوصف: Neuronal ceroid lipofuscinosis type 2 (CLN2 disease) is a progressive neurodegenerative disease that results in early-onset, severe, progressive, neurological disabilities, leading to death in late childhood or early adolescence. Management has relied on symptomatic care, and supportive and palliative strategies, but the approval of the enzyme replacement therapy cerliponase alfa in the USA and Europe in 2017 brought different treatment opportunities. We describe the natural history of CLN2 disease, its diagnosis and management, and the preclinical and clinical development of cerliponase alfa. A PubMed search was undertaken for cerliponase alfa and rhTPP1 to identify preclinical and clinical studies. The hallmark-presenting symptoms of CLN2 disease are unprovoked seizures and a history of language delay, and progression involves motor dysfunction, and cognitive and visual decline. Cerliponase alfa has shown efficacy and tolerability in mouse and canine models of CLN2 disease when delivered intracerebroventricularly. Administration of cerliponase alfa in patients with CLN2 disease has led to significant reductions in the rate of decline of motor and language functions in comparison with a natural history population. The approval of cerliponase alfa has brought a new era for CLN2 disease, highlighting the need to understand different patterns of disease progression and clinical needs in treated patients.
اللغة: English
تدمد: 1178-203X
1176-6336
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::2863691a7be4f4bbeb8a75ad7d1bbb5dTest
http://europepmc.org/articles/PMC7127909Test
حقوق: OPEN
رقم الانضمام: edsair.pmid..........2863691a7be4f4bbeb8a75ad7d1bbb5d
قاعدة البيانات: OpenAIRE