US 11,992,524 B2
Compositions and methods for therapeutic or vaccine delivery
Jacqueline Fischer-Lougheed, Duarte, CA (US); Bradford H. Steele, Pasadena, CA (US); Cecilia Roh, South Pasadena, CA (US); and Robert G. Johnson, Lafayette, CA (US)
Assigned to Genvivo, Inc., San Marino, CA (US)
Filed by GenVivo, Inc., San Marino, CA (US)
Filed on Oct. 24, 2022, as Appl. No. 18/049,267.
Claims priority of provisional application 63/413,188, filed on Oct. 4, 2022.
Claims priority of provisional application 63/271,675, filed on Oct. 25, 2021.
Prior Publication US 2023/0277647 A1, Sep. 7, 2023
Int. Cl. A61K 39/12 (2006.01); A61K 39/145 (2006.01); A61P 31/14 (2006.01); A61K 39/00 (2006.01)
CPC A61K 39/12 (2013.01) [A61K 39/145 (2013.01); A61P 31/14 (2018.01); A61K 2039/5256 (2013.01); A61K 2039/575 (2013.01)] 19 Claims
 
1. A method of treating or preventing a disease or condition in a subject by administration of a recombinant retroviral vector with defective retroviral integration activity, comprising administering to the subject a recombinant retroviral vector comprising a first nucleic acid sequence encoding a mutant integrase and a second nucleic acid sequence encoding at least one payload comprising an antigen, said mutant integrase, when compared to a wild-type integrase having a sequence of SEQ ID NO: 1, comprises at least one mutation in a Mg2+ binding motif of a catalytic core domain selected from the group consisting of D125A, D184A, and E220A; wherein the recombinant retroviral vector has defective retroviral integration activity as compared to a recombinant retroviral vector comprising the wild-type integrase, wherein the at least one payload is expressed in the subject for at least three days, wherein the recombinant retroviral vector is a recombinant murine leukemia virus (MLV), and wherein the antigen induces an immune response in the subject, thereby treating or preventing the disease or condition in the subject.