发明名称 |
METHODS FOR ENGINEERING ALLOGENEIC AND HIGHLY ACTIVE T CELL FOR IMMUNOTHERAPHY |
摘要 |
The present invention relates to methods for developing engineered T-cells for immunotherapy that are non-alloreactive. The present invention relates to methods for modifying T-cells by inactivating both genes encoding T-cell receptor and an immune checkpoint gene to unleash the potential of the immune response. This method involves the use of specific rare cutting endonucleases, in particular TALE-nucleases (TAL effector endonuclease) and polynucleotides encoding such polypeptides, to precisely target a selection of key genes in T-cells, which are available from donors or from culture of primary cells. The invention opens the way to standard and affordable adoptive immunotherapy strategies for treating cancer and viral infections. |
申请公布号 |
US2016120905(A1) |
申请公布日期 |
2016.05.05 |
申请号 |
US201414889686 |
申请日期 |
2014.05.13 |
申请人 |
CELLECTIS |
发明人 |
GALETTO Roman;GOUBLE Agnes;GROSSE Stephanie;SCHIFFER-MANNIOUI Cécile;POIROT Laurent;SCHARENBERG Andrew;SMITH Julianne |
分类号 |
A61K35/17;C12N5/0783 |
主分类号 |
A61K35/17 |
代理机构 |
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代理人 |
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主权项 |
1) A method of preparing T-cell(s) for immunotherapy comprising:
(a) modifying T-cell(s) by inactivating at least:
a first gene encoding a immune checkpoint protein, anda second gene encoding a component of the T-cell receptor (TCR); and (b) expanding said T-cell(s). |
地址 |
Paris FR |