{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,1]],"date-time":"2026-05-01T21:15:26Z","timestamp":1777670126251,"version":"3.51.4"},"reference-count":81,"publisher":"SAGE Publications","issue":"19-20","license":[{"start":{"date-parts":[[2020,10,1]],"date-time":"2020-10-01T00:00:00Z","timestamp":1601510400000},"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":[[2020,10]]},"abstract":"<jats:p>\n                    Recombinant adeno-associated viral (rAAV) vector mobilization is a largely theoretical process in which intact AAV vectors spread or \u201cmobilize\u201d from transduced cells and infect additional cells within, or external of, the initial host. This process can be helper virus-independent (vector alone) or helper virus-dependent (\n                    <jats:italic toggle=\"yes\">de novo<\/jats:italic>\n                    rAAV production facilitated by superinfection of both wild-type AAV [wtAAV] and Adenovirus 5 [Ad] helper virus). Herein, rAAV production and mobilization with and without wtAAV were analyzed following plasmid transfection or viral transduction utilizing well-established\n                    <jats:italic toggle=\"yes\">in vitro<\/jats:italic>\n                    conditions and analytical measurements. During\n                    <jats:italic toggle=\"yes\">in vitro<\/jats:italic>\n                    production, wtAAV produced the highest titer with rAAV-luc (4.1\u2009kb), rAAV-IDUA (3.7\u2009kb), and rAAV-Nano-dysferlin (4.9\u2009kb) generating 2.5-, 5.9-, or 10.7-fold lower amounts, respectively. Surprisingly, cotransfection of a wtAAV and an rAAV plasmid resulted in a uniform decrease in production of wtAAV in all instances with a concomitant increase of rAAV such that wtAAV:rAAV titers were at a ratio of 1:1 for all constructs investigated. These results were shown to be independent of the rAAV transgenic sequence, size, transgene, or promoter choice and point to novel aspects of wtAAV complementation that enhance current vector production systems yet to be defined. In a mobilization assay, a sizeable amount of rAAV recovered from infected 293 cell lysate remained intact and competent for a secondary round of infection (termed Ad-independent mobilization). In rAAV-infected cells coinfected with Ad and wtAAV, rAAV particle production was increased &gt;50-fold compared with no Ad conditions. In addition, Ad-dependent rAAV vectors mobilized and resulted in &gt;1,000-fold transduction upon a subsequent second-round infection, highlighting the reality of these theoretical safety concerns that can be manifested under various conditions. Overall, these studies document and signify the need for mobilization-resistant vectors and the opportunity to derive better vector production systems.\n                  <\/jats:p>","DOI":"10.1089\/hum.2020.118","type":"journal-article","created":{"date-parts":[[2020,8,24]],"date-time":"2020-08-24T03:55:05Z","timestamp":1598241305000},"page":"1054-1067","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":16,"title":["Adeno-Associated Virus Vector Mobilization, Risk Versus Reality"],"prefix":"10.1177","volume":"31","author":[{"given":"Liujiang","family":"Song","sequence":"first","affiliation":[{"name":"Gene Therapy Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA;"},{"name":"Department of Ophthalmology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R. 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