IP Library Granted Patent US 12,178,832
Granted Patent B2
US 12,178,832 · App. 17/307,754 · Granted Dec 31, 2024

Methods for the production of TCR gamma delta + t cells

Inventors: Diogo Antonio Remechido Anjos (Cantanhede, PT); Daniel Vargas Correia (Cantanhede, PT); Afonso Rocha Martins De Almeida (Cantanhede, PT)
Assignee: GammaDelta Therapeutics Ltd
A61K35/17C12N5/0638A61K2039/5158C12N2501/2301C12N2501/2302C12N2501/2304C12N2501/2307C12N2501/2315C12N2501/2321C12N2501/24C12N2501/515C12N2501/599
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Quick Facts
Patent No.
US 12,178,832
App. No.
17/307,754
Granted
Dec 31, 2024
Kind
B2
Abstract

The present invention relates to novel methods for the isolation and the selective ex vivo expansion of V32′ TCRy6+ T cells and to their clinical application.

Claims (22)

1. A method of modulating an immune response comprising administering an effective amount of TCRγδ+ T cells obtained by a method for expanding Vδ2-TCRγδ+ T cells in a sample comprising:

(1) culturing cells in the sample in a first culture medium comprising a T cell mitogen and interleukin-4; in the absence of interleukin-15, interleukin-2, or interleukin-7; and

(2) culturing the cells obtained in step (1) in a second culture medium comprising a T cell mitogen and interleukin-15, interleukin-2, or interleukin-7, in the absence of interleukin-4, to an animal in need thereof.

2. A method according to claim 1 , wherein the first or second culture medium, or both culture media, further comprise a second, a third and a fourth growth factor.

3. A method according to claim 2 , wherein said growth factors are interferon-γ, interleukin-21 and interleukin-1β or a mimetic or functional equivalent thereof.

4. A method according to claim 1 , wherein the first and second culture media further contain serum or plasma.

5. A method according to claim 1 , wherein prior to step (1) the cells in the sample are enriched for T cells; enriched for TCRγδ+ T cells; depleted of TCRαβ+ T cells; first depleted of TCRαβ+ T cells, and then enriched for CD3+ cells; or depleted of non-TCRγδ+ T cells.

6. A method according to claim 1 , wherein the sample is blood or tissue or fractions thereof.

7. A method according to claim 6 , wherein the sample is selected from peripheral blood, umbilical cord blood, lymphoid tissue, epithelia, thymus, bone marrow, spleen, liver, cancerous tissue, infected tissue, lymph node tissue or fractions thereof.

8. A method according to claim 1 , wherein in the first culture medium the T cell mitogen is present in an amount from about 10 to about 5000 ng/ml and interleukin-4 is present in an amount from about 1 to about 1000 ng/ml.

9. A method according to claim 1 , wherein in the second culture medium the T cell mitogen is present in an amount from about 0.1 to about 50 μg/ml and interleukin-15 is present in an amount from about 1 to about 1000 ng/ml.

10. A method according to claim 1 , wherein the T cell mitogen is an antibody or a fragment thereof.

11. A method for treating an infection comprising administering an effective amount of TCRγδ+ T cells obtained by a method for expanding Vδ2-TCRγδ+ T cells in a sample comprising:

(1) culturing cells in the sample in a first culture medium comprising a T cell mitogen and interleukin-4; in the absence of interleukin-15, interleukin-2, or interleukin-7; and

(2) culturing the cells obtained in step (1) in a second culture medium comprising a T cell mitogen and interleukin-15, interleukin-2, or interleukin-7, in the absence of interleukin-4, to an animal in need thereof.

12. A method for treating cancer comprising administering an effective amount of TCRγδ+ T cells obtained by a method for expanding Vδ2-TCRγδ+ T cells in a sample comprising:

(1) culturing cells in the sample in a first culture medium comprising a T cell mitogen and interleukin-4; in the absence of interleukin-15, interleukin-2, or interleukin-7; and

(2) culturing the cells obtained in step (1) in a second culture medium comprising a T cell mitogen and interleukin-15, interleukin-2, or interleukin-7, in the absence of interleukin-4, to an animal in need thereof.

13. The method according to claim 12 , wherein the cancer is chronic lymphocytic leukemia, chronic myelogenous leukemia, acute myelogenous leukemia, acute lymphoblastic leukemia, and T cell and B cell leukemias, lymphomas (Hodgkin's and non-Hodgkin's), lymphoproliferative disorders, plasmacytomas, histiocytomas, melanomas, adenomas, sarcomas, carcinomas of solid tissues, hypoxic tumors, squamous cell carcinomas, genitourinary cancers such as cervical and bladder cancer, hematopoietic cancers, head and neck cancers, and nervous system cancers.

14. A method for vaccinating an animal comprising administering an effective amount of TCRγδ+ T cells obtained by a method for expanding Vδ2-TCRγδ+ T cells in a sample comprising:

(1) culturing cells in the sample in a first culture medium comprising a T cell mitogen and interleukin-4; in the absence of interleukin-15, interleukin-2, or interleukin-7; and

(2) culturing the cells obtained in step (1) in a second culture medium comprising a T cell mitogen and interleukin-15, interleukin-2, or interleukin-7, in the absence of interleukin-4, to an animal in need thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 19, 2023
From: LYMPHACT - LYMPHOCYTE ACTIVATION TECHNOLOGIES, S.A.
To: GAMMADELTA THERAPEUTICS LIMITED
Reel/Frame 065911/0918 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2021
From: ANJOS, DIOGO ANTONIO REMECHIDO; CORREIA, DANIEL VARGAS; MARTINS DE ALMEIDA, AFONSO ROCHA
To: LYMPHACT - LYMPHOCYTE ACTIVATION TECHNOLOGIES, S.A.
Reel/Frame 057197/0856 →
Priority Claims (2)
PT 20151000047568 · Jun 9, 2015 · national
PT 20161000032002 · May 12, 2016 · national
Continuity (2)
Division 15735371
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