Methods of generating chimeric adenoviruses and uses for such chimeric adenoviruses
AssigneeThe Trustees of the University of Pennsylvania
InventorsSoumitra Roy, James M. Wilson
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AssigneeThe Trustees of the University of Pennsylvania
InventorsSoumitra Roy, James M. Wilson
Estimating the term…
A method for providing an adenovirus from a serotype which does not grow efficiently in a desired cell line with the ability to grow in that cell line is described. The method involves replacing the left and right termini of the adenovirus with the corresponding termini from an adenovirus which grow efficiently in the desired cell line. At a minimum, the left terminus spans the (5′) inverted terminal repeat, the left terminus spans the E4 region and the (3′) inverted terminal repeat. The resulting chimeric adenovirus contains the internal regions spanning the genes encoding the penton, hexon and fiber from the serotype which does not grow efficiently in the desired cell. Also provided are vectors constructed from novel simian adenovirus sequences and proteins, host cells containing same, and uses thereof.
A chimeric adenovirus comprising a hexon protein of an adenovirus serotype which is incapable of efficient growth in a selected host cell selected from the group consisting of C1, Pan6, and Ad40, said chimeric adenovirus comprising:
A chimeric adenovirus comprising a hexon protein of a C1 adenovirus, said chirneric adenovirus comprising:
Dependencies are inferred from the claim text.