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Planet of the AAVs: The Spinal Cord Injury Episode

K. Stepankova, P. Jendelova, L. Machova Urdzikova

. 2021 ; 9 (6) : . [pub] 20210528

Jazyk angličtina Země Švýcarsko

Typ dokumentu časopisecké články, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/bmc21017653

Grantová podpora
19-10365S Grant Agency of the Czech Republic
CZ.02.1.01/0.0/0.0/15_003/0000419 Center of Reconstruction Neuroscience - NEURORECON
320421 Charles University Grant Agency

The spinal cord injury (SCI) is a medical and life-disrupting condition with devastating consequences for the physical, social, and professional welfare of patients, and there is no adequate treatment for it. At the same time, gene therapy has been studied as a promising approach for the treatment of neurological and neurodegenerative disorders by delivering remedial genes to the central nervous system (CNS), of which the spinal cord is a part. For gene therapy, multiple vectors have been introduced, including integrating lentiviral vectors and non-integrating adeno-associated virus (AAV) vectors. AAV vectors are a promising system for transgene delivery into the CNS due to their safety profile as well as long-term gene expression. Gene therapy mediated by AAV vectors shows potential for treating SCI by delivering certain genetic information to specific cell types. This review has focused on a potential treatment of SCI by gene therapy using AAV vectors.

Citace poskytuje Crossref.org

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