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21.
公开(公告)号:US20240309397A1
公开(公告)日:2024-09-19
申请号:US18530878
申请日:2023-12-06
Applicant: Cellectis
Inventor: Roman GALETTO , Agnes GOUBLE , Stephanie GROSSE , Cecile MANNIOUI , Laurent POIROT , Andrew SCHARENBERG , Julianne SMITH
IPC: C12N15/85 , A61K35/17 , A61K38/00 , A61K39/00 , C07K14/705 , C07K14/725 , C07K16/28 , C12N5/0783
CPC classification number: C12N15/85 , A61K35/17 , C07K14/7051 , C07K14/70517 , C07K14/70521 , C07K14/70578 , C07K16/28 , C07K16/2803 , C12N5/0636 , A61K38/00 , A61K39/00 , C07K2317/14 , C07K2317/24 , C07K2317/569 , C07K2317/622 , C07K2319/00 , C07K2319/03 , C07K2319/74 , C12N2501/39 , C12N2501/51 , C12N2501/515 , C12N2501/599 , C12N2502/99 , C12N2510/00
Abstract: Methods for developing engineered T-cells for immunotherapy that are both non-alloreactive and resistant to immunosuppresive drugs. The present invention relates to methods for modifying T-cells by inactivating both genes encoding target for an immunosuppressive agent and T-cell receptor, in particular genes encoding CD52 and TCR. 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.
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公开(公告)号:US20230050345A1
公开(公告)日:2023-02-16
申请号:US17715218
申请日:2022-04-07
Applicant: CELLECTIS
Inventor: Roman GALETTO , Agnes GOUBLE , Stephanie GROSSE , Cécile SCHIFFER-MANNIOUI , Laurent POIROT , Andrew SCHARENBERG , Julianne SMITH
IPC: A61K35/17 , C12N5/0783 , C07K16/28 , C07K14/725 , C07K14/705 , C12N15/85
Abstract: 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.
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23.
公开(公告)号:US20220177914A1
公开(公告)日:2022-06-09
申请号:US17674436
申请日:2022-02-17
Applicant: Cellectis
Inventor: Roman GALETTO , Agnes GOUBLE , Stephanie GROSSE , Cecile MANNIOUI , Laurent POIROT , Andrew SCHARENBERG , Julianne SMITH
IPC: C12N15/85 , A61K35/17 , C07K14/705 , C12N5/0783 , C07K14/725 , C07K16/28
Abstract: A method of expanding TCRalpha deficient T-cells by expressing pTalpha or functional variants thereof into said cells, thereby restoring a functional CD3 complex. This method is particularly useful to enhance the efficiency of immunotherapy using primary T-cells from donors. This method involves the use of pTalpha or functional variants thereof and polynucleotides encoding such polypeptides to expand TCRalpha deficient T-cells. Such engineered cells can be obtained by using specific rare-cutting endonuclease, preferably TALE-nucleases. The use of Chimeric Antigen Receptor (CAR), especially multi-chain CAR, in such engineered cells to target malignant or infected cells. The invention opens the way to standard and affordable adoptive immunotherapy strategies for treating cancer and viral infections.
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公开(公告)号:US20210060079A1
公开(公告)日:2021-03-04
申请号:US17099608
申请日:2020-11-16
Applicant: Cellectis
Inventor: Roman GALETTO , Julianne SMITH , Andrew SCHARENBERG , Cécile SCHIFFER-MANNIOUI
IPC: A61K35/17 , C07K14/705 , C12N5/0783 , C07K14/725 , C07K16/28
Abstract: The present invention relates to chimeric antigen receptors (CAR). CARs are able to redirect immune cell specificity and reactivity toward a selected target exploiting the ligand-binding domain properties. In particular, the present invention relates to a Chimeric Antigen Receptor in which extracellular ligand binding is a scFV derived from a CD19 monoclonal antibody, preferably 4G7. The present invention also relates to polynucleotides, vectors encoding said CAR and isolated cells expressing said CAR at their surface. The present invention also relates to methods for engineering immune cells expressing 4G7-CAR at their surface which confers a prolonged “activated” state on the transduced cell. The present invention is particularly useful for the treatment of B-cells lymphomas and leukemia.
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25.
公开(公告)号:US20190216853A1
公开(公告)日:2019-07-18
申请号:US16361370
申请日:2019-03-22
Applicant: Cellectis
Inventor: Roman GALETTO , Agnes GOUBLE , Stephanie GROSSE , Cecile MANNIOUI , Laurent POIROT , Andrew SCHARENBERG , Julianne SMITH
IPC: A61K35/17 , C07K14/705 , C12N5/0783 , C07K14/725 , C07K16/28
Abstract: A method of expanding TCRalpha deficient T-cells by expressing pTalpha or functional variants thereof into said cells, thereby restoring a functional CD3 complex. This method is particularly useful to enhance the efficiency of immunotherapy using primary T-cells from donors. This method involves the use of pTalpha or functional variants thereof and polynucleotides encoding such polypeptides to expand TCRalpha deficient T-cells. Such engineered cells can be obtained by using specific rare-cutting endonuclease, preferably TALE-nucleases. The use of Chimeric Antigen Receptor (CAR), especially multi-chain CAR, in such engineered cells to target malignant or infected cells. The invention opens the way to standard and affordable adoptive immunotherapy strategies for treating cancer and viral infections.
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公开(公告)号:US20190002573A1
公开(公告)日:2019-01-03
申请号:US15925182
申请日:2018-03-19
Applicant: CELLECTIS
Inventor: Roman GALETTO
IPC: C07K16/28 , C07K14/725 , A61K39/00
Abstract: The present invention relates to Chimeric Antigen Receptors (CAR) that are recombinant chimeric proteins able to redirect immune cell specificity and reactivity toward selected membrane antigens, and more particularly in which extracellular ligand binding is a scFV derived from a CD123 monoclonal antibody, conferring specific immunity against CD123 positive cells. The engineered immune cells endowed with such CARs are particularly suited for treating lymphomas and leukemia.
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公开(公告)号:US20180051089A1
公开(公告)日:2018-02-22
申请号:US15546623
申请日:2016-01-25
Applicant: Cellectis
Inventor: Roman GALETTO , Barbara Johnson SASU , Arvind RAJPAL , Philippe DUCHATEAU , Alexandre JUILLERAT , Julien VALTON , Mathieu SIMON
IPC: C07K16/28 , A61K35/17 , A61K39/00 , C07K14/725 , C07K16/30 , C12N5/00 , C12N5/0783
CPC classification number: C07K16/2866 , A61K35/17 , A61K39/0011 , A61K39/39558 , A61K2039/505 , A61K2039/5156 , A61K2039/5158 , A61K2039/6056 , A61K2039/64 , C07K14/7051 , C07K14/70517 , C07K14/70535 , C07K14/70578 , C07K16/2803 , C07K16/2887 , C07K16/3061 , C07K2317/24 , C07K2317/53 , C07K2317/56 , C07K2317/622 , C07K2319/00 , C07K2319/02 , C07K2319/03 , C12N5/0093 , C12N5/0636 , C12N5/0638 , C12N2510/00 , G01N15/1031 , G01N15/14 , G01N2015/008 , G01N2015/1006 , G01N2015/1081 , G01N2015/149
Abstract: The present invention relates to a TCR KO—or TCR KO and dCK KO—engineered immune cells expressing a Chimeric Antigen Receptors (CAR) specific for CD123 that is a recombinant chimeric protein able to redirect immune cell specificity and reactivity toward CD123-expressing cells, and more particularly in which extracellular ligand binding is a scFV derived from a CD123 monoclonal antibody, conferring specific immunity against CD123 positive cells. The engineered immune cells endowed with such CD123 CARs are particularly suited for treating relapse refractory AML and blastic plasmacytoid dendritic cell neoplasm and for use as a treatment before bone marrow transplantation.
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28.
公开(公告)号:US20170360835A1
公开(公告)日:2017-12-21
申请号:US15659792
申请日:2017-07-26
Applicant: Cellectis
Inventor: Roman GALETTO , Agnes GOUBLE , Stephanie GROSSE , Cecile MANNIOUI , Laurent POIROT , Andrew SCHARENBERG , Julianne SMITH
IPC: A61K35/17 , C07K16/28 , C12N5/0783 , C07K14/725 , C07K14/705 , A61K38/00
CPC classification number: A61K35/17 , A61K38/00 , C07K14/7051 , C07K14/70517 , C07K14/70521 , C07K14/70578 , C07K16/28 , C07K16/2803 , C07K2317/14 , C07K2317/24 , C07K2317/569 , C07K2317/622 , C07K2319/00 , C07K2319/03 , C07K2319/74 , C12N5/0636 , C12N2501/39 , C12N2501/51 , C12N2501/515 , C12N2501/599 , C12N2502/99 , C12N2510/00
Abstract: A method of expanding TCRalpha deficient T-cells by expressing pTalpha or functional variants thereof into said cells, thereby restoring a functional CD3 complex. This method is particularly useful to enhance the efficiency of immunotherapy using primary T-cells from donors. This method involves the use of pTalpha or functional variants thereof and polynucleotides encoding such polypeptides to expand TCRalpha deficient T-cells. Such engineered cells can be obtained by using specific rare-cutting endonuclease, preferably TALE-nucleases. The use of Chimeric Antigen Receptor (CAR), especially multi-chain CAR, in such engineered cells to target malignant or infected cells. The invention opens the way to standard and affordable adoptive immunotherapy strategies for treating cancer and viral infections.
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公开(公告)号:US20170145094A1
公开(公告)日:2017-05-25
申请号:US15301686
申请日:2015-04-02
Applicant: CELLECTIS
Inventor: Roman GALETTO
IPC: C07K16/28 , C07K14/725 , C07K14/705
CPC classification number: C07K16/2803 , A61K2039/505 , C07K14/7051 , C07K14/70517 , C07K2317/24 , C07K2317/53 , C07K2317/62 , C07K2317/622 , C07K2317/73 , C07K2319/03
Abstract: The present invention relates to Chimeric Antigen Receptors (CAR) that are recombinant chimeric proteins able to redirect immune cell specificity and reactivity toward selected membrane antigens, and more particularly in which extracellular ligand binding is a scFV derived from a CD33 monoclonal antibody, conferring specific immunity against CD33 positive cells. The engineered immune cells endowed with such CARs are particularly suited for treating lymphomas and leukemia.
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