-
公开(公告)号:US11993809B2
公开(公告)日:2024-05-28
申请号:US17260572
申请日:2019-07-17
IPC分类号: C12Q1/6841 , C12N15/10 , C12Q1/6876
CPC分类号: C12Q1/6841 , C12N15/1065 , C12N15/1096 , C12Q1/6876 , C12Q2600/16
摘要: The present invention relates to a method for analyzing a biological sample on a single cell level by compartmentalizing said sample using a grid and performing an optimized combinatorial indexing protocol within cells of the compartmentalized tissue while deducing cell-specific information regarding the cell identity and activity in the spatial context within the sample.
-
公开(公告)号:US11643468B2
公开(公告)日:2023-05-09
申请号:US16641181
申请日:2018-08-23
发明人: Uta Höpken , Armin Rehm , Julia Bluhm , Wolfgang Uckert
IPC分类号: C07K16/28 , A61K35/17 , C07K14/725 , C07K14/705 , C12N5/0783 , A61P35/00
CPC分类号: C07K16/2866 , A61K35/17 , A61P35/00 , C07K14/7051 , C07K14/70521 , C12N5/0636 , C12N5/0646 , C07K2317/24 , C07K2317/565 , C07K2317/622 , C07K2317/73 , C07K2319/02 , C07K2319/03 , C07K2319/33 , C12N2510/00
摘要: An isolated chimeric antigen receptor polypeptide (CAR), wherein the CAR comprises an extracellular antigen-binding domain, comprising an antibody or antibody fragment that binds a human CXC chemokine receptor type 5 (CXCR5) protein. Also disclosed is a nucleic acid molecule encoding the CAR of the invention, a genetically modified immune cell, preferably a T cell, expressing the CAR of the invention and the use of said cell in the treatment of a medical disorder associated with the presence of pathogenic cells expressing CXCR5, preferably pathogenic mature B cells and/or memory B cells, and/or pathogenic T cells and/or T follicular helper cells, in particular mature B cell non-Hodgkin's lymphoma (B-NHL), T cell non-Hodgkin's lymphoma, or autoantibody-dependent autoimmune disease, preferably selected from systemic lupus erythematosus (SLE) or rheumatoid arthritis.
-
公开(公告)号:US20220363732A1
公开(公告)日:2022-11-17
申请号:US17621931
申请日:2020-06-30
申请人: MAX-DELBRÜCK-CENTRUM FÜR MOLEKULARE MEDIZIN IN DER HELMHOLTZ -GEMEINSCHAFT , CHARITÉ - UNIVERSITÄTSMEDIZIN BERLIN
IPC分类号: C07K14/725 , C12N15/113
摘要: The present invention is directed to the field of immunotherapy, in particular, adoptive T cell therapy or T cell receptor (TCR) gene therapy of cancer. The invention provides nucleic acids encoding at least one TCR alpha or beta chain construct of a TCR construct capable of specifically binding to a peptide from the T-cell lineage specific antigen CD5, preferably SEQ ID NO: 1 or 33, in the context of a human MHC I such as HLA-A*02, in particular HLA-A*02:01. The invention also provides corresponding proteins and host cells, preferably, CD8+ T cells, expressing said TCR construct. Treatment optionally is in the context of allogeneic stem cell transplantation, in particular, mismatch-transplantation, or haploidentical transplantation, or in combination with an agent capable of inhibiting expression of HLA-A*02 in the TCR-transgenic T cells. The invention thus also provides compositions and kits comprising the nucleic acids of the invention in combination with an agent capable of inhibiting expression of HLA-A*02, and, as well as the medical use of such compositions and kits. The nucleic acids, compositions and kits, proteins or host cells may be for use in the diagnosis, prevention and/or treatment of a CD5-positive T-cell lymphoma or T-cell leukemia, no matter whether the antigen is expressed on the cell surface, intracytoplasmic or in both manners.
-
公开(公告)号:US11331290B2
公开(公告)日:2022-05-17
申请号:US16775156
申请日:2020-01-28
发明人: Ulrike Stein , Wolfgang Walther , Ulrike Sack , Peter M. Schlag
IPC分类号: A61K31/167 , A61K31/4035 , A61K45/06 , A61P35/00
摘要: A method for inhibiting, reducing and/or reducing the risk of cancer metastasis in a subject, including identifying a subject as in need of inhibiting, reducing and/or reducing the risk of cancer metastasis, by identifying the subject as having a cancer with an elevated or up-regulated level of S100A4 transcription compared to a level in non-oncogenic cells, and administering to the subject a therapeutically effective amount of niclosamide or a niclosamide derivate, thereby inhibiting or reducing S100A4 transcription, so as to inhibit, reduce and/or reduce the risk of cancer metastasis, wherein 15 to 400 mg niclosamide or niclosamide derivate is administered per kg body weight of the subject (mg/kg), 1 or 2 times daily.
-
公开(公告)号:US20220125807A1
公开(公告)日:2022-04-28
申请号:US17310756
申请日:2020-02-21
申请人: Max-Delbrück-Centrum für Molekulare Medizin in der Holmholtz-Gemeinschafft , Charité - Universitätsmedizin Berlin
IPC分类号: A61K31/635 , A61K31/167 , A61K31/192 , A61K31/423 , A61K31/519 , A61K31/63 , A61K31/5415 , A61K31/40 , A61K31/366 , A61K31/405 , A61K31/47 , A61K31/22 , A61K31/505 , A61K31/4184 , A61K31/4523 , A61P35/00
摘要: A pharmaceutical combination, includes an inhibitor of the Wnt/β-catenin signaling pathway and an inhibitor of MACC1. One combination includes an inhibitor of S100A4 as a Wnt-signaling inhibitor, preferably niclosamide, and a statin or MEK1 inhibitor as an inhibitor of MACC1. A pharmaceutical composition can include the combination. The combination or composition can be used in the treatment of a tumor disease, such as a solid tumor, and/or for the treatment and/or prophylaxis of tumor metastasis.
-
6.
公开(公告)号:US20220064256A1
公开(公告)日:2022-03-03
申请号:US17414471
申请日:2019-12-17
申请人: MAX-DELBRÜCK-CENTRUM FÜR MOLEKULARE MEDIZIN IN DER HELMHOLTZ-GEMEINSCHAFT , CHARITÉ - UNIVERSITÄTSMEDIZIN BERLIN
IPC分类号: C07K14/725 , C07K14/705 , C07K14/71 , A61P35/00
摘要: The present invention is directed to the field of immunotherapy, in particular, adoptive T cell therapy or T cell receptor (TCR) gene therapy of cancer, in particular, of B cell lymphoma or B cell leukemia. The invention provides a nucleic acid encoding TCR alpha or beta chain constructs of TCR constructs capable of specifically binding to a peptide of SEQ ID NO: 1, derived from the lineage specific antigen CD22, in the context of HLA-A2 and to subsequently lyse CD22-positive cells. The invention further provides a corresponding protein and host cell, e.g., a CD8+ T cell, pharmaceutical compositions comprising the same, and therapeutic use for treatment of B cell lymphoma or B cell leukemia, such as diffuse large B-cell lymphoma (DLBCL).
-
7.
公开(公告)号:US11028104B2
公开(公告)日:2021-06-08
申请号:US16867835
申请日:2020-05-06
发明人: Michael Bader , Edgar Specker , Susann Matthes , Anja Schütz , Keven Mallow , Maik Grohmann , Marc Nazaré
摘要: The invention relates to a xanthine derivative defined by chemical formula I or a salt thereof, its use as a medicament, especially for use in the treatment of serotonin-related diseases or disorders, and a pharmaceutical preparation comprising the xanthine derivative. The novel xanthine compounds are capable of inhibiting tryptophan hydroxylases (TPH) involved in the biosynthesis of serotonin and are effective in influencing the serotonin level in the body.
-
公开(公告)号:US20210061876A1
公开(公告)日:2021-03-04
申请号:US16958604
申请日:2019-01-02
申请人: Max-Delbrück-Centrum für Molekulare Medizin in der Helmholtz-Gemeinschaft , Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts , Imperial College Innovations Limited , Charité - Universitätsmedizin Berlin
发明人: Thomas BLANKENSTEIN , Gerald WILLIMSKY , Juliane LIEPE , Peter Michael KLOETZEL , Michele MISHTO , Christin BEIER
IPC分类号: C07K14/725 , A61K38/00 , A61K39/00
摘要: The present invention pertains to antigen recognizing constructs against tumor specific proteasome splicing variants. The invention in particular provides novel T cell receptor (TCR) based molecules which are selective and specific for tumor cells carrying antigenic epitopes generated by proteasome peptide splicing of tumor specific antigens. The TCRs of the invention, and antigen binding fragments derived therefrom, are of use for the diagnosis, treatment and prevention of proliferative diseases, preferably for the treatment of cancer. Further provided are nucleic acids encoding the antigen recognizing constructs of the invention, vectors comprising these nucleic acids, recombinant cells expressing the antigen recognizing constructs and pharmaceutical compositions comprising the compounds of the invention.
-
公开(公告)号:US20200155484A1
公开(公告)日:2020-05-21
申请号:US16775156
申请日:2020-01-28
发明人: ULRIKE STEIN , WOLFGANG WALTHER , ULRIKE SACK , PETER M. SCHLAG
IPC分类号: A61K31/167 , A61K31/4035 , A61K45/06
摘要: A method for inhibiting, reducing and/or reducing the risk of cancer metastasis in a subject, including identifying a subject as in need of inhibiting, reducing and/or reducing the risk of cancer metastasis, by identifying the subject as having a cancer with an elevated or up-regulated level of S100A4 transcription compared to a level in non-oncogenic cells, and administering to the subject a therapeutically effective amount of niclosamide or a niclosamide derivate, thereby inhibiting or reducing S100A4 transcription, so as to inhibit, reduce and/or reduce the risk of cancer metastasis, wherein 15 to 400 mg niclosamide or niclosamide derivate is administered per kg body weight of the subject (mg/kg), 1 or 2 times daily.
-
10.
公开(公告)号:US20200063096A1
公开(公告)日:2020-02-27
申请号:US16563089
申请日:2019-09-06
IPC分类号: C12N5/0735 , C12N5/074
摘要: An in vitro method for identifying, isolating and/or enriching primate naive pluripotent stem cells, the method including analyzing transcription of a type 7 long terminal repeat (LTR7) nucleic acid sequence of a type H human endogenous retrovirus (HERVH) (LTR7/HERVH-associated transcription), and identifying, isolating and/or enriching primate naive pluripotent stem cells based on LTR7/HERVH-associated transcription, wherein LTR7/HERVH-associated transcription is a marker for primate naive pluripotent stem cells. An isolated in vitro population of primate naive pluripotent stem cells is obtained by the method, wherein in the cells LTR7/HERVH-associated transcription is elevated in comparison to control cells, wherein control cells are primed pluripotent stem cells or differentiated cells.
-
-
-
-
-
-
-
-
-