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公开(公告)号:US11166987B2
公开(公告)日:2021-11-09
申请号:US15773524
申请日:2016-11-17
Applicant: Universität Basel
Inventor: Simon Ittig , Marlise Amstutz , Christoph Kasper , Guy R. Cornelis
IPC: A61K39/02 , A61P35/00 , A61K39/00 , A61K39/112 , A61K39/104 , C12N15/74 , A61K35/74
Abstract: The present invention relates to recombinant virulence attenuated Gram-negative bacterial strains for use in a method of treating a malignant solid tumor in a subject.
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公开(公告)号:US20210267709A1
公开(公告)日:2021-09-02
申请号:US17254737
申请日:2019-06-21
Applicant: UNIVERSITÄT BASEL
Inventor: Georg RAUTER , Ivan SUSIC
Abstract: A force sensing device is disclosed that includes a housing tip, a plurality of sensors stationarily spaced from each other, and a spring element connecting the housing tip to the sensors such that moving the housing tip and the sensor relative to each other causes a resilient deformation of the spring element. The spring element is configured to arrange the housing tip in a zero position relative to the sensors by a spring force of the spring element. The force sensing device is also equipped with a spring tensioning structure configured to adapt the spring force of the spring element.
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公开(公告)号:US11091591B2
公开(公告)日:2021-08-17
申请号:US15760398
申请日:2016-09-14
Applicant: UNIVERSITÄT BASEL
Inventor: Ruben Herrendorff , Beat Ernst , Andreas Steck , Hélène Pfister , Giulio Navarra
Abstract: The invention relates to carbohydrate ligands and moieties, respectively, mimicking glycoepitopes comprised by glycosphingolipids of the nervous system, particularly glycoepitopes comprised by glycosphingolipids of the cerebroside, the globoside-, the ganglioside- and the sulfoglucuronyl paragloboside type, which are bound by anti-glycan antibodies associated with neurological diseases. The invention further relates to the use of these carbohydrate ligands/moieties, in diagnosis as well as for the treatment of neurological diseases associated with anti-glycan antibodies. In particular, the invention relates to compounds of formula (I) and (II) and to therapeutically acceptable polymers comprising a multitude of these compounds, including polymers with loading of one compound of formula (I) or (II) or combinations of several compounds of formula (I), and/or (II). The compounds of formula (I) are defined as: wherein RI1 is Z or wherein RI2 is H, SO3H, or wherein RI3 is H or wherein RI4 is H or wherein RI5 and RI6 are independently H or wherein RI7 is H or and compounds of formula (II) are defined as: wherein RII1 is Z or wherein RII2 is Z or wherein Z is —N(Ra)—A—B—CH2—(CH2)q—SH, wherein Ra is H, C1-C4-alky, C1-C4alkoxy, CH2C6H5, CH2CH2C6H5, OCH2C6H5, or OCH2CH2C6H5; A is C1-C7-alkylene, C1-C7-alkoxy, C1-C4-alkyl—(OCH2CH2)pO—C1-C4-alkyl, or C1-C7-alkoxy-Rb, wherein Rb is an optionally substituted aryl or an optionally substituted heteroaryl, and wherein p is 0 to 6, preferably p is 1, 2 or 3, and further preferably p is 1; B is NHC(O), S or CH2; q is 0 to 6, preferably q is 1, 2, 3 or 4, and further preferably q is 1 or 2.
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公开(公告)号:US20210061838A1
公开(公告)日:2021-03-04
申请号:US16848268
申请日:2020-04-14
Applicant: UNIVERSITÄT BASEL
Inventor: Beat Ernst , Ruben Herrendorff , Andreas Steck , Fan Yang
IPC: C07H15/207 , C07H15/203 , C08G69/10 , C08G69/48 , G01N33/68 , C08F2/00 , C08F120/36
Abstract: The invention relates to carbohydrate ligands presenting the minimal Human Natural Killer-1 (HNK-1) epitope that bind to anti-MAG (myelin-associated glycoprotein) IgM antibodies, and their use in diagnosis as well as for the treatment of anti-MAG neuropathy. In particular, the invention relates to disaccharides of formula (I) and (II) wherein Z is optionally substituted phenyl, heteroaryl, arylcarbonyl, or heteroarylmethyl, and to therapeutically acceptable polymers comprising a multitude of substituents of formula (I) and/or formula (II), wherein Z is a bifunctional linker connecting the disaccharides to the polymer backbone.
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公开(公告)号:US10823756B2
公开(公告)日:2020-11-03
申请号:US14910704
申请日:2014-08-06
Applicant: UNIVERSITÄT BASEL
Inventor: Marko Loparic
IPC: G01Q30/20
Abstract: The invention relates to a sample holder (1) for holding a sample, particularly for use with an atomic force microscope. According to the invention, the sample holder (1) comprises: preferably a flexible support (10) having an upper side (10a) and a lower side (10b) facing away from said upper side (10a), a first and a second holding member (100, 200), wherein each holding member (100, 200) comprises a first section (101, 201) that is preferably connected to the upper side (10a) of the flexible support (10), as well as an opposing second section (102, 202) forming a tip (103, 203) of the respective holding member (100, 200), such that the holding members (100, 200) are each movable from a first position, in which the tips (103, 203) are positioned adjacent to one another, into a second position, in which the tips (103, 203) are further apart from each other than in said first positions and are separated by a gap (G) for receiving at least a portion of the sample (S) to be held, and wherein said tips (103, 203) are designed to penetrate the sample (S) or to press against it so as to hold it when the sample (S) is received by said gap (G) and the holding members (100, 200) are moved back from the second positions into the first positions.
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公开(公告)号:US20190389926A1
公开(公告)日:2019-12-26
申请号:US16563987
申请日:2019-09-09
Applicant: UNIVERSITÄT BASEL
Inventor: Gennaro DE LIBERO , Marco LEPORE , Lucia MORI
IPC: C07K14/725 , C12N5/0783 , G01N1/30 , G01N33/569 , C12N5/09 , C12N15/85 , A61P35/00 , A61K35/17
Abstract: The invention relates to a method of isolating a T cell that expresses a T cell receptor capable of binding specifically to an antigen presented by a cancer cell in association with an MR1 molecule. The method comprises the steps of (a) providing a preparation of T cells, (b) contacting the preparation with cancer cells expressing MR1 protein; (c) isolating a T cell that is specifically reactive to said cancer cells.The invention further relates to a method of preparing a T cell preparation expressing select MR1 recognizing T cell receptors from transgene expression vectors, the use of such T cell preparations in treatment of cancer, and to collections of MR1 reactive T cell receptor encoding nucleic acids and cells.
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公开(公告)号:US20160324947A1
公开(公告)日:2016-11-10
申请号:US15101214
申请日:2014-12-02
Applicant: VIROMETIX AG , SWISS TROPICAL AND PUBLIC HEALTH INSTITUTE , UNIVERSITÄT BASEL , UNIVERSITÄT ZÜRICH
Inventor: Arin Ghasparian , Armando Zuniga , Nina Geib , Marco Tamborini , Maja Jud , Gerd Pluschke , Aniebrys Marrero Nodarse , John Anthony Robinson
IPC: A61K39/09 , C07K14/315
CPC classification number: A61K39/092 , A61K2039/5258 , A61K2039/55511 , A61K2039/55516 , A61K2039/575 , A61K2039/6018 , C07K14/3156 , C07K2319/73
Abstract: The invention relates to lipopeptides consisting of a peptide chain comprising a parallel coiled-coil domain, a proline-rich peptide antigen, and a lipid moiety, all covalently linked, which aggregate to synthetic virus-like particles. Proline-rich peptide antigens considered contain negatively and positively charged amino acid, and at least 15% of the amino acids are proline. Such synthetic virus-like particles carrying proline-rich antigens derived from pneumococcal proteins are useful as vaccines against infectious diseases caused by Gram-positive bacteria such as Streptococcus pneumoniae.
Abstract translation: 本发明涉及由包含平行卷曲螺旋结构域,富含脯氨酸肽抗原和脂质部分的肽链组成的脂肽,其全部共价连接,其聚集成合成病毒样颗粒。 认为富含脯氨酸的肽抗原含有带正电荷的氨基酸,至少15%的氨基酸是脯氨酸。 携带来自肺炎球菌蛋白质的富含脯氨酸的抗原的合成病毒样颗粒可用作针对由革兰氏阳性菌如肺炎链球菌引起的感染性疾病的疫苗。
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公开(公告)号:US20250152609A1
公开(公告)日:2025-05-15
申请号:US18840197
申请日:2023-02-22
Applicant: PHARMALP SA , UNIVERSITÄT BASEL
Inventor: PHILIPPE MEUWLY , OLIVIER POTTERAT , BRUNO SCHNYDER
IPC: A61K31/60 , A61K9/00 , A61K31/593 , A61K31/7004 , A61K31/7048 , A61K36/73 , A61P31/04
Abstract: The present invention is directed to compounds, compositions, uses and methods useful in the prevention or treatment of urinary infections, in particular E. coli infections and in particular recurrent urinary infections.
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公开(公告)号:US20240344031A1
公开(公告)日:2024-10-17
申请号:US18682918
申请日:2022-08-02
Applicant: UNIVERSITÄT BASEL
Inventor: Sebastien PIGEOT , Ivan MARTIN , Paul BOURGINE
IPC: C12N5/0775 , C07K14/51 , C12N5/077 , C12N9/12 , C12N9/64
CPC classification number: C12N5/0662 , C07K14/51 , C12N5/0655 , C12N9/1276 , C12N9/6472 , C12N2506/1346 , C12N2510/00 , C12N2533/90 , C12Y207/07049 , C12Y304/22036
Abstract: A mesenchymal stem/stromal (MSC) cell line, in particular a human mesenchymal stem cell (hMSC), capable of chondrogenic differentiation when cultured in a chondrogenic medium, comprising a first transgene comprising a first nucleic acid sequence encoding for a preferably mammalian immortalizing enzyme under control of a first promoter sequence operable in said mesenchymal cell and a second transgene comprising a second nucleic acid sequence encoding a preferably mammalian bone morphogenic protein under control of a second promoter sequence operable in said mesenchymal cell.
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公开(公告)号:US20240343718A1
公开(公告)日:2024-10-17
申请号:US18526732
申请日:2023-12-01
Applicant: TORQUR AG , UNIVERSITÄT BASEL
Inventor: Denise RAGEOT , Paul HEBEISEN , Florent BEAUFILS , Doriano FABBRO , Petra HILLMAN-WULLNER , Hoa Huu Phuc NGUYEN , Wolfgang LOSCHER , Claudia BRANDT , Alexander Markus SELE
IPC: C07D413/14 , A61K31/53 , A61K31/5377 , A61K31/5386 , A61K31/541 , A61P25/08 , A61P25/28 , C07D417/14 , C07D451/02 , C07D451/14 , C07D498/08 , C07D519/00
CPC classification number: C07D413/14 , A61K31/53 , A61K31/5377 , A61K31/5386 , A61K31/541 , A61P25/08 , A61P25/28 , C07D417/14 , C07D451/02 , C07D451/14 , C07D498/08 , C07D519/00
Abstract: The present invention is relates to a compound of formula (I), wherein X1, X2 and X3 are, independently of each other, N or CH; with the proviso that at least two of X1X2 and X3 are N; Y is N or CH; R1 and R2 are independently of each other (iii) a morpholinyl of formula (II) wherein the arrow denotes the bond in formula (I); and wherein R3 and R4 are independently of each other H, C1-C3alkyl optionally substituted with one or two OH, C1-C2fhioroalkyl, C1-C2alkoxy, C1-C2alkoxyC1-C3alkyl, CN, or C(0)0-C1-C2alkyl; or R3 and R4 form together a bivalent residue —R5R6- selected from Ci-C3alkylene optionally substituted with 1 to 4 F, —CH2-0-CH2—, —CH2—NH—CH2—, or any of the structures wherein the arrows denote the bonds in formula (II); or (iv) a saturated 6-membered heterocyclic ring Z selected from thiomorpholinyl and piperazinyl, optionally substituted by 1 to 3 R7; wherein R7 is independently at each occurrence Ci-C3alkyl optionally substituted with one or two OH, C1-C2fluoroalkyl, C1-C2alkoxyC1-C3 alkyl, C3-C6cycloalkyl; or two R7 substituents form together a bivalent residue —R8R9— selected from C1-C3alkylene optionally substituted with 1 to 4 F, —CH2-0-CH2— or —O—CH2CH2-0-; with the proviso that at least one of R1 and R2 is a morpholinyl of formula II; and prodrugs, metabolites, tautomers, solvates and pharmaceutically acceptable salts thereof, for use in the prevention or treatment of a neurological disorder in a subject.
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