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Modified gamma delta t cells and uses thereof

a technology of gamma delta t cells, which is applied in the field of modified, can solve the problems that studies have not realized the potential to use car modified t cells from one subj

Pending Publication Date: 2021-08-19
TC BIOPHARM LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent describes a new method to treat cancer by using a type of T cell called gamma delta T cells. These cells can be modified to recognize and attack cancer cells using a special technique called Chimeric Antigen Receptors (CARs). The patent describes a method for putting CARs into gamma delta T cells. This approach has not been previously known and may have advantages over previous methods. The technical effect of this patent is to open up a new way to use gamma delta T cells to treat cancer.

Problems solved by technology

However, such studies have not realised the potential to utilise CAR modified γδT cells from one subject to provide therapy to a second different subject (allogeneic use).

Method used

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  • Modified gamma delta t cells and uses thereof
  • Modified gamma delta t cells and uses thereof
  • Modified gamma delta t cells and uses thereof

Examples

Experimental program
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Effect test

example 1

[0176]PBMCs were isolated by density centrifugation (lymphoprep) from leukapheresis material and cryopreserved. PBMCs were resuscitated and zoledronic acid (5 μM) stimulated PBMCs were cultured in the presence of IL-2 (1000 IU / mL) and 5% human AB serum in growth media. After 48 hours in culture (37° C., 5% CO2, humidified atmosphere), cells were transduced with lentivirus containing a lenti-CMV-MCS-EF1a-puro construct with either a classical CAR sequence (anti-CD19 scFv-CD28-CD137-CD3) or a co-stimulatory CAR sequence (anti-CD19 scFv-CD28-CD137) and 5 μg / mL polybrene at an MOI of 10. Transduction was repeated 24 hours later. CAR mRNA expression was verified by QPCR using universal primers which detected expression of both constructs at day 5. Specific expression of each construct was confirmed using a combination of the discriminatory primers and universal primers (as per FIGS. 5, 6).

example 2

[0177]Cells were transduced with lentivirus containing classical CAR sequence and expanded as described in example 1. 7 days following transduction, cytotoxic activity was assessed by co-culturing transduced or non-transduced γδT cells with CD19 positive target cell lines, Daudi or Ramos. Target cell lines were stained with the non-toxic membrane dye PKH67 (5 μM) for specific visualisation of the CD19 target population using flow cytometry. Following a 4.5 hour co-incubation with γδT cells or classical-CAR expressing γδT cells, co-cultures were stained with annexin V and propidium iodide (PI) to visualise apoptotic cells. The % specific cell death was calculated in the target cell population only. CAR-transduced γδT cells elicited increased potency in CD19 positive target cells in comparison to non-transduced γδT cells (FIG. 7).

example 3

[0178]Cells were transduced with lentivirus containing classical CAR or costimulatory CAR sequence and expanded as described in example 1. The CD19 positive target cell lines Daudi and Ramos were pre-treated for 24 hours+ / −5 μM zoledronic acid. Cytotoxic activity was assessed as described in example 2. PKH67-stained target cells (+ / −zometa pre-treatment) were co-cultured with transduced or non-transduced γδT cells. The co-stimulatory CAR expressing γδT cells exhibited similar cytotoxicity towards the CD19 positive target cells as the classical-CAR expressing γδT cells, despite the absence of the CD3 activation domain, signal 1 instead provided via activation through the γδTCR by IPP sensing. Both CARs provided enhanced cytotoxicity towards γδT cells when compared to non-transduced γδT cells (FIG. 8).

[0179]Although the invention has been particularly shown and described with reference to particular examples, it will be understood by those skilled in the art that various changes in th...

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Abstract

The present invention provides composition and methods for the treatment of cancer or infectious diseases in a human. The invention includes the generation and administration of gamma delta T cells that express chimeric antigen receptors (CARs) comprising an antigen binding domain, a hinge domain, a transmembrane domain, a costimulatory signalling domain with the inclusion or not of a CD3 zeta signalling domain. Expression of CAR sequence omitting the CD3 zeta signalling domain in gamma delta T cells, provides for a CAR-T therapy in vivo, which will effect cytolysis only on target cells providing ligands for activation of the gamma delta T cell receptor (TCR).

Description

FIELD OF THE INVENTION[0001]This application relates to methods of preparing and using gamma delta T cells (γδT cells), suitably the use of gamma delta T cells in allogeneic or autologous recipient subjects for the treatment of conditions including virus infection, fungal infection, protozoal infection and cancer, specifically to the use of chimeric antigen receptors (CARs) modified γδT cells. The invention also relates to processes for the generation of γδT cells expressing chimeric antigen receptors and for detecting CAR expression. In addition, the present invention relates to the pharmaceutical use of the cells generated with the processes discussed herein in the treatment of diseases such as cancer and infectious disease.[0002]Gamma delta T lymphocytes represent a minor subset of peripheral blood in humans (less than 10%). Gamma delta T cells expressing Vγ9Vδ2 (gamma 9 delta 2) T cell receptor recognise the endogenous isopentenyl pyrophosphate (IPP) that is over produced in can...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K35/17C07K14/725C12N5/0783A61K31/00
CPCA61K35/17C07K14/7051C12N5/0638A61K31/00C12N2501/2302C07K2319/02C07K2319/03C07K2319/00C07K2317/53C07K2317/732C07K2317/92C12N2510/00C12N15/86C12N2740/15043A61K45/06A61P35/00A61K2039/505A61K39/464412A61K39/4611A61K39/4631A61P31/00A61P31/04A61P31/10A61P31/12A61P33/02A61P43/00C07K2317/622
Inventor LEEK, MICHAEL DAVIDHANNIGAN, ADELEPATAKAS, AGAPITOSPARUZINA, DARIA
Owner TC BIOPHARM LTD
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