IP Library Granted Patent US 9,862,927
Granted Patent B2
US 9,862,927 · App. 13/011,798 · Granted Jan 9, 2018

Dendritic cell vaccines

Inventors: Jacques F. Banchereau (Dallas, TX); Monica Montes (Dallas, TX); Anna Karolina Palucka (Dallas, TX); Louis M. Sloan (Dallas, TX); Yves Levy (Paris, FR)
Assignees: Baylor Research Institute; Agence Nationale de Recherches Sur le Sida Et Les Hepatitis Virales
C12N5/0639A61K39/12A61K39/21C07K14/005A61K2039/5154A61K2039/545A61K2039/6018C12N2501/052C12N2501/22C12N2501/24C12N2740/16222C12N2740/16234C12N2740/16322C12N2740/16334
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Quick Facts
Patent No.
US 9,862,927
App. No.
13/011,798
Granted
Jan 9, 2018
Kind
B2
Abstract

Compositions and methods for the prophylaxis and treatment of human immunodeficiency virus (HIV) infections are disclosed herein. More specifically the present invention discloses describes an autologous dendritic cell (DC) vaccine product derived by culturing a patient's monocytes with granulocyte macrophage colony stimulating factor (GM-CSF) and interferon alpha 2b (IFN-α), loading the DC with a mixture of five lipopeptides of Gag, Nef and Pol HIV antigens, and, optionally activating the DC with lipopolysaccharide (LPS).

Claims (27)

1. A method of inducing a therapeutic immune response against a human immunodeficiency virus (HIV) infection in a patient comprising:

injecting into the patient a composition comprising autologous dendritic cells (DCs) loaded with a lipopeptide mixture comprising five HIV antigenic peptides,

wherein the five HIV antigen peptides are Gag p17(17-35) (SEQ ID NO: 1), Gag p24(253-284) (SEQ ID NO: 2), Nef(66-97) (SEQ ID NO: 3), Nef (116-145) (SEQ ID NO: 4), and Pol(325-355) (SEQ ID NO: 5) and wherein the therapeutic immune response includes an increase in CD4+ T cells that secrete IL-2.

2. The method of claim 1 , further comprising the step of activating the lipopeptide loaded DCs with a lipopolysaccharide.

3. The method of claim 1 , wherein the HIV antigenic peptides are linked to a lipid by a covalent bond between the C-terminal group of the peptide and a palmitolyl-lysylamide group of a lipid.

4. The method of claim 1 , further comprising administering to the patient one or more anti-viral therapies selected from Highly Active AntiRetroviral Therapy (HAART), protease inhibitors, reverse transcriptase inhibitors or nucleotide analogs.

5. The method of claim 1 , further comprising determining whether the patient has developed antibodies against the HIV antigenic peptides after injecting the composition.

6. The method of claim 1 , further comprising formulating the composition as a pharmaceutically acceptable formulation.

7. The method of claim 1 , further comprising generating the composition comprising the following steps:

isolating monocytes comprising one or more DCs from the blood of the patient;

loading the lipopeptide mixture; and isolating the loaded DCs.

8. The method of claim 2 , further comprising:

washing activated and loaded DCs;

resuspending the activated and loaded DCs in a freezing solution in a suitable container; and

freezing the solution in the suitable container.

9. The method of claim 7 , wherein the monocytes are stimulated by cytokines comprising a granulocyte macrophage colony stimulating factor (GM-CSF) and an interferon alpha 2b (IFN-α).

10. A method of inducing a therapeutic immune response against a human immunodeficiency virus (HIV) infection in a patient comprising:

loading dendritic cells (DCs) from the patient with a lipopeptide mixture comprising five antigenic HIV peptides;

isolating the loaded DCs; and,

injecting the loaded DCs into the patient,

wherein the five antigenic peptides are Gag p17(17-35) (SEQ ID NO: 1), Gag p24(253-284) (SEQ ID NO: 2), Nef(66-97) (SEQ ID NO: 3), Nef (116-145) (SEQ ID NO: 4), and Pol(325-355) (SEQ ID NO: 5) and wherein the therapeutic immune response includes an increase in CD4+ T cells that secrete IL-2.

11. A method of inducing a therapeutic immune response against a human immunodeficiency virus (HIV) infection in a patient comprising:

loading dendritic cells (DCs) from the patient with a lipopeptide mixture comprising five antigenic HIV peptides;

activating the loaded dendritic cells with a lipopolysaccharide; and, injecting the loaded DCs into the patient,

wherein the five antigenic peptides are Gag p17(17-35) (SEQ ID NO: 1), Gag p24(253-284) (SEQ ID NO: 2), Nef(66-97) (SEQ ID NO: 3), Nef (116-145) (SEQ ID NO: 4), and Pol(325-355) (SEQ ID NO: 5) and wherein the therapeutic immune response includes an increase in CD4+ T cells that secrete IL-2.

12. The method of claim 1 , wherein the patient is determined to have been infected with HIV.

13. A method for increasing CD4+ T cells that secrete IL-2 in a patient comprising injecting into the patient a composition comprising autologous dendritic cells (DCs) loaded with a lipopeptide mixture comprising Gag p17(17-35) (SEQ ID NO: 1), Gag p24(253-284) (SEQ ID NO: 2), Nef(66-97) (SEQ ID NO: 3), Nef(116-145) (SEQ ID NO: 4), and Pol(325-355) (SEQ ID NO: 5), wherein CD4+ T cells that secrete IL-2 are increased in the patient.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 22, 2012
From: LEVY, YVES
To: AGENCE NATIONALE DE RECHERCHES SUR LE SIDA ET LES HEPATITIS VIRALES
Reel/Frame 027743/0069 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2011
From: BANCHEREAU, JACQUES F.; MONTES, MONICA; PALUCKA, ANNA KAROLINA; SLOAN, LOUIS M.
To: BAYLOR RESEARCH INSTITUTE
Reel/Frame 026606/0621 →
Continuity (3)
Provisional Application 61297555 · Jan 22, 2010
Provisional Application 61375829 · Aug 21, 2010
Related Publication 20110182937A1 · Jul 28, 2011