TY - JOUR T1 - Astrocyte-selective AAV-ADAMTS4 gene therapy combined with hindlimb rehabilitation promotes functional recovery after spinal cord injury JF - bioRxiv DO - 10.1101/797696 SP - 797696 AU - Jarred M. Griffin AU - Barbara Fackelmeier AU - Connor A. Clemett AU - Dahna M. Fong AU - Alexandre Mouravlev AU - Deborah Young AU - Simon J. O’Carroll Y1 - 2019/01/01 UR - http://biorxiv.org/content/early/2019/10/15/797696.abstract N2 - Chondroitin sulphate proteoglycans (CSPGs) are inhibitors to axon regeneration and plasticity. Bacterial chondroitinase ABC degrades CSPGs and has been extensively reported to be therapeutic after SCI but there remain concerns for its clinical translation. A disintegrin and metalloproteinase with thrombospondin motifs-4 (ADAMTS4) is a human enzyme that catalyses the proteolysis of CSPG protein cores. Infusion of ADAMTS4 into the damaged spinal cord was previously shown to improve functional recovery after SCI, however, this therapy is limited in its enzyme form. Adeno-associated viral (AAV) vector gene therapy has emerged as the vector of choice for safe, robust and long-term transgene expression in the central nervous system. Here, an AAV expression cassette containing ADAMTS4 under the control of the astrocytic GfaABC1D promoter was packaged into an AAV5 vector. Sustained expression of ADAMTS4 was achieved in vitro and in vivo, leading to widespread degradation of CSPGs. AAV-ADAMTS4 resulted in significantly decreased lesion size, increased sprouting of hindlimb corticospinal tract axons, increased serotonergic fiber density caudal to the injury, and improved functional recovery after moderate contusive SCI. Hindlimb-specific exercise rehabilitation was used to drive neuroplasticity towards improving functional connections. The combination of hindlimb rehabilitation with AAV-ADAMTS4 led to enhanced functional recovery after SCI. Thus, widespread and long-term degradation of CSPGs through AAV-ADAMTS4 gene therapy in a combinational approach with rehabilitation represents a promising candidate for further preclinical development.AAVAdeno-associated virusADAMTSA disintegrin and metalloproteinase with thrombospondin motifsChABCChondroitinase ABCCS-GAGChondroitin sulphate glycosaminoglycanCSPGChondroitin sulphate proteoglycanECMExtracellular matrixGAGGlycosaminoglycanLVLentiviral vector ER -