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Hum Gene Ther ; 33(9-10): 541-549, 2022 05.
Artigo em Inglês | MEDLINE | ID: mdl-34963343

RESUMO

Osteoarthritis (OA) is a disabling, degenerative disease characterized by progressive cartilage and bone damage. There remains a need for local therapies that, following a single injection, can provide long-term pain relief and functional improvement and potentially delay disease progression. FX201 is a novel, intra-articular (IA), interleukin-1 receptor antagonist (IL-1Ra) gene therapy in development for the treatment of OA. In this study, we assessed the efficacy, biodistribution, and safety of helper-dependent adenovirus (HDAd)-ratIL-1Ra, the rat surrogate of FX201, and the biodistribution of FX201, in the anterior cruciate ligament transection (ACLT) rat OA model. A single IA injection of HDAd-ratIL-1Ra administered 7 days post-ACLT mitigated OA-related changes to cartilage, bone, and the synovial membrane at week 12 following surgery. Furthermore, FX201 and HDAd-ratIL-1Ra persisted for at least 92 days in the injected joint and proximal tissues with minimal evidence of vector spreading peripherally. Finally, HDAd-ratIL-1Ra showed a favorable safety profile without any local or systemic adverse effects. In conclusion, HDAd-ratIL-1Ra demonstrated local therapeutic and disease-modifying effects and was well tolerated, supporting further clinical development of FX201.


Assuntos
Proteína Antagonista do Receptor de Interleucina 1 , Osteoartrite , Adenoviridae/genética , Animais , Modelos Animais de Doenças , Terapia Genética , Injeções Intra-Articulares , Proteína Antagonista do Receptor de Interleucina 1/genética , Osteoartrite/genética , Osteoartrite/metabolismo , Osteoartrite/terapia , Ratos , Membrana Sinovial/metabolismo , Distribuição Tecidual
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