{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T08:48:48Z","timestamp":1790153328313,"version":"4.0.1"},"reference-count":55,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2019,1,1]],"date-time":"2019-01-01T00:00:00Z","timestamp":1546300800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Human Gene Therapy"],"published-print":{"date-parts":[[2019,1]]},"abstract":"<jats:p>\n                    Pompe disease is an autosomal recessive glycogen storage disorder caused by deficiency of the lysosomal enzyme acid alpha-glucosidase (GAA). GAA deficiency results in systemic lysosomal glycogen accumulation and cellular disruption in muscle and the central nervous system (CNS). Adeno-associated virus (AAV) gene therapy is ideal for Pompe disease, since a single systemic injection may correct both muscle and CNS pathologies. Using the Pompe mouse (B6;129-Gaa\n                    <jats:sup>Tm1Rabn<\/jats:sup>\n                    \/J), this study sought to explore if AAVB1, a newly engineered vector with a high affinity for muscle and CNS, reduces systemic weakness and improves survival in adult mice. Three-month-old\n                    <jats:italic toggle=\"yes\">\n                      Gaa\n                      <jats:sup>\u2013\/\u2013<\/jats:sup>\n                    <\/jats:italic>\n                    animals were injected with either AAVB1 or AAV9 vectors expressing\n                    <jats:italic toggle=\"yes\">GAA<\/jats:italic>\n                    and tissues were harvested 6 months later. Both AAV vectors prolonged survival. AAVB1-treated animals had a robust weight gain compared to the AAV9-treated group. Vector genome levels, GAA enzyme activity, and histological analysis indicated that both vectors transduced the heart efficiently, leading to glycogen clearance, and transduced the diaphragm and CNS at comparable levels. AAVB1-treated mice had higher GAA activity and greater glycogen clearance in the tongue. Finally, AAVB1-treated animals showed improved respiratory function comparable to wild-type animals. In conclusion, AAVB1-\n                    <jats:italic toggle=\"yes\">GAA<\/jats:italic>\n                    offers a promising therapeutic option for the treatment of muscle and CNS in Pompe disease.\n                  <\/jats:p>","DOI":"10.1089\/hum.2018.016","type":"journal-article","created":{"date-parts":[[2018,6,14]],"date-time":"2018-06-14T09:25:38Z","timestamp":1528968338000},"page":"57-68","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":47,"title":["Systemic Delivery of AAVB1-\n                    <i>GAA<\/i>\n                    Clears Glycogen and Prolongs Survival in a Mouse Model of Pompe Disease"],"prefix":"10.1177","volume":"30","author":[{"given":"Allison M.","family":"Keeler","sequence":"first","affiliation":[{"name":"Division of Pulmonary Medicine, Department of Pediatrics, University of Massachusetts Medical School, Worcester Massachusetts."},{"name":"Horae Gene Therapy Center, University of 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