Method to treat cancer with engineered T-cells

• US 10,639,329 B2
• Filed: 06/12/2016
• Issued: 05/05/2020
• Est. Priority Date: 06/12/2015
• Status: Active Grant

• Current Assignee: Lentigen Technology Inc. (Miltenyi GmbH)
• Original Assignee: Lentigen Technology Inc. (Miltenyi GmbH)
• Inventors: Dropulic, Boro, Orentas, Rimas, Schneider, Dina, Krueger, Winfried
• Primary Examiner(s): Leavitt, Maria G
• Application Number:
  US15/735,921
• Publication Number:
  US 20190134091A1
• Time in Patent Office: 1,423 Days
• Field of Search: None
• CPC Class Codes: A61K 2039/5156 expressing foreign proteins
• CPC Class Codes: A61K 2039/5158 Antigen-pulsed cells, e.g. T-cells
• CPC Class Codes: A61K 38/177 Receptors; Cell surface antigens; Cell surface determinants
• CPC Class Codes: A61K 38/1774 Immunoglobulin superfamily (e.g. CD2, CD4, CD8, ICAM molecules, B7 molecules, Fc-receptors, MHC-molecules)
• CPC Class Codes: A61K 39/4611 T-cells, e.g. tumor infiltrating lymphocytes [TIL], lymphokine-activated killer cells [LAK] or regulatory T cells [Treg]
• CPC Class Codes: A61K 39/4631 Chimeric Antigen Receptors [CAR]
• CPC Class Codes: A61K 39/4632 T-cell receptors [TCR]; antibody T-cell receptor constructs
• CPC Class Codes: A61K 39/464499 Undefined tumor antigens, e.g. tumor lysate or antigens targeted by cells isolated from tumor
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: A61P 35/02 specific for leukemia
• CPC Class Codes: A61P 7/00 Drugs for disorders of the blood or the extracellular fluid
• CPC Class Codes: C07K 14/7051 T-cell receptor (TcR)-CD3 complex
• CPC Class Codes: C07K 2319/03 containing a transmembrane segment
• CPC Class Codes: C12N 2502/1121 Dendritic cells
• CPC Class Codes: C12N 2510/00 Genetically modified cells
• CPC Class Codes: C12N 2740/16043 viral genome or elements thereof as genetic vector
• CPC Class Codes: C12N 5/0636 T lymphocytes

Abstract

Novel adoptive immunotherapy compositions comprising co-cultured lentiviral vector-transduced autologous antigen presentation cells and T cells are provided herein as well as are methods of use of same in a patient-specific combination immunotherapy that can be used to treat cancers and other diseases and conditions.

Claims

1. A method of treating a human patient having a solid tumor expressing CD19, the method comprising administering to the patient a pharmaceutical composition comprising an anti-tumor effective amount of an autologous T-cell population transduced with one or more lentiviral vectors encoding single or multiple chimeric antigen receptors (CARs), the single or multiple CARs comprising an isolated nucleic acid sequence selected from the group consisting of SEQ ID NO:

13, SEQ ID NO;

17, and SEQ ID NO;

21 to promote in vivo expansion and persistence of the autologous patient-specific anti-tumor T-cells,

wherein the T-cells are co-cultured with autologous dendrite cells differentiated from monocytes, the autologous dendrite cells being transduced with one or more lentiviral vectors expressing patient-derived tumor antigens,

wherein the T-cell population is additionally transduced with one or more lentiviral vectors encoding tumor-specific T-cell receptors (TCRs) thereby generating an active patient-specific autologous anti-tumor T-cell population capable of recognizing patient-derived tumor antigens which can be infused directly back into the patient to result in tumor stabilization, tumor reduction, elimination of cancer, or remission of cancer in a patient-specific manner.

3. The method of claim 1, wherein the T cell has been preselected by virtue of expressing specific activation or memory-associated surface markers.

4. The method of claim 1, wherein the T cell and dendritic cells are derived from a hematopoietic stem cell donor, and wherein the procedure is carried out in the context of hematopoietic stem cell transplantation.

2. A method of treating a human patient having a solid tumor the method comprising administering to the patient a pharmaceutical composition comprising an anti-tumor effective amount of an autologous T-cell population transduced with one or more lentiviral vectors encoding single or multiple chimeric antigen receptors (CARs), the single or multiple CARs comprising an anti-CD19, an anti-CD20, or an anti-CD22 antibody or binding fragment thereof, wherein the anti-CD19 CAR comprises an isolated nucleic acid sequence selected from the group consisting of SEQ ID NO:

13, SEQ ID NO;

17, and SEQ ID NO;

21,

wherein the T-cell population is additionally transduced with one or more lentiviral vectors encoding tumor-specific T-cell receptors (TCRs) to generate an active patient-specific autologous anti-tumor T-cell population capable of recognizing patient-derived CD19, CD20, or CD22 tumor antigens which can be infused directly back into the patient to promote in vivo expansion, persistence of patient-specific anti-tumor T-cells resulting in tumor stabilization, tumor reduction, elimination of cancer, or remission of cancer in a patient-specific manner.

5. The method of claim 2, wherein the T cell has been preselected by virtue of expressing specific activation or memory-associated surface markers.

6. The method of claim 2, wherein the T cell and dendritic cells are derived from a hematopoietic stem cell donor, and wherein the procedure is carried out in the context of hematopoietic stem cell transplantation.