IP Library Patent Application 15150373
Patent Application
App. No. 15/150,373

DUAL VECTOR FOR INHIBITION OF HUMAN IMMUNODEFICIENCY VIRUS

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Patent No.
US None
App. No.
15/150,373
Abstract

The present invention provides an expression vector for preventing or inhibiting HIV entry, fusion or replication in mammalian cells. In particular, the invention provides a recombinant retroviral vector that encodes an inhibitor of a HIV co-receptor, such as CCR5 or CXCR4, and a protein that inhibits HIV fusion to target cells and/or HIV replication. Pharmaceutical compositions comprising such constructs and methods of use thereof to prevent or treat HIV infection in a patient are also disclosed.

Claims (27)

1 . (canceled)

2 . A method of treating or preventing HIV infection in a patient comprising (i) transducing hematopoietic cells with an expression vector, the expression vector comprising a first nucleic acid sequence encoding an inhibitor of an HIV co-receptor and a second nucleic acid sequence encoding a protein that inhibits HIV fusion to a target cell or HIV replication, and (ii) transplanting said transduced hematopoietic cells in the patient, wherein said transduced hematopoietic cells are resistant to HIV infection.

3 . The method of claim 2 , wherein said hematopoietic cells are hematopoietic progenitor/stem cells (HPSC), CD4+ T lymphocytes, CD8+ T lymphocytes, monocyte/macrophages, or combinations thereof.

4 . The method of claim 4 , wherein said transplanted HPSC generate granulocytes, monocyte/macrophages, and lymphocytes that are resistant to HIV infection.

5 . The method of claim 2 , wherein said hematopoietic cells are autologous or allogeneic.

6 . The method of claim 2 , wherein said first nucleic acid sequence encodes a siRNA or shRNA having a double-stranded region, said double-stranded region comprising a sequence that is substantially identical and complementary to a sequence of CCR5.

7 . The method of claim 6 , wherein the shRNA has a sequence of SEQ ID NO: 1.

8 . The method of claim 6 , wherein said transduced hematopoietic cells express reduced levels of CCR5 protein as compared to non-transduced hematopoietic cells.

9 . The method of claim 2 , wherein said second nucleic acid sequence encodes a C46 protein.

10 . (canceled)

11 . (canceled)

12 . The method of claim 4 , wherein said granulocytes, monocyte/macrophages, and lymphocytes are resistant to infection by R5 and X4 tropic strains of HIV.

13 . The method of claim 12 , wherein said granulocytes, monocyte/macrophages, and lymphocytes are resistant to infection by HAART-resistant HIV strains.

14 - 17 . (canceled)

18 . A method of treating or preventing HIV infection in a patient comprising administering a pharmaceutical composition to patient, the pharmaceutical composition comprising (i) an expression vector comprising a first nucleic acid sequence encoding an inhibitor of an HIV co-receptor and a second nucleic acid sequence encoding a protein that inhibits HIV fusion to a target cell or HIV replication; and (ii) a pharmaceutically acceptable carrier.

19 . The method of claim 18 , wherein the patient is resistant to infection by R5 and X4 tropic strains of HIV following administration of the composition.

20 . The method of claim 19 , wherein the patient is resistant to infection by HAART-resistant HIV strains following administration of the composition.

21 - 24 . (canceled)

25 . A method of treating or preventing HIV infection in a patient comprising:

(i) transducing hematopoietic cells with an expression vector, the expression vector comprising a first nucleic acid sequence encoding a shRNA having a sequence of SEQ ID NO: 1, and a second nucleic acid sequence encoding a C46 protein, and

(ii) transplanting said transduced hematopoietic cells in the patient, wherein said transduced hematopoietic cells are resistant to HIV infection.

26 . The method of claim 25 , wherein said first and second nucleic acid sequences are operably linked to a promoter.

27 . The method of claim 25 , wherein said hematopoietic cells are hematopoietic progenitor/stem cells (HPSC), CD4+ T lymphocytes, CD8+ T lymphocytes, monocyte/macrophages, or combinations thereof.

28 . The method of claim 25 , wherein said transplanted HPSC generate granulocytes, monocyte/macrophages, and lymphocytes that are resistant to HIV infection.

29 . The method of claim 25 , wherein said hematopoietic cells are autologous or allogeneic.

30 . The method of claim 28 , wherein said granulocytes, monocyte/macrophages, and lymphocytes are resistant to infection by R5 and X4 tropic strains of HIV.

31 . The method of claim 28 , wherein said granulocytes, monocyte/macrophages, and lymphocytes are resistant to infection by HAART-resistant HIV strains.

Assignments (5)
CHANGE OF NAME Recorded Oct 21, 2020
From: CALIMMUNE, INC.
To: CSL BEHRING GENE THERAPY, INC.
Reel/Frame 054157/0943 →
RELEASE OF SECURITY INTEREST Recorded Jun 26, 2018
From: SILICON VALLEY BANK
To: CALIMMUNE, INC.
Reel/Frame 046428/0370 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2017
From: MILLINGTON, MICHELLE L; BOYD, MAUREEN P; SYMONDS, GEOFFREY P; BRETON, LOUIS RANDALL
To: CALIMMUNE INC.
Reel/Frame 043746/0142 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 19, 2017
From: CHEN, IRVIN S.Y.; AN, DONG SUNG
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 043339/0434 →
SECURITY INTEREST Recorded Apr 11, 2017
From: CALIMMUNE, INC.
To: SILICON VALLEY BANK
Reel/Frame 041971/0910 →