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公开(公告)号:US20240350606A1
公开(公告)日:2024-10-24
申请号:US18665046
申请日:2024-05-15
发明人: YOU-WEN HE , HEQIANG SUN , THOMAS AUGUST , JUN LIU , YADONG WEI
IPC分类号: A61K39/00 , A61K39/245 , A61P35/00 , C07K14/005 , C07K14/47 , C12N15/85
CPC分类号: A61K39/001192 , A61K39/0008 , A61K39/001104 , A61K39/001106 , A61K39/001109 , A61K39/001184 , A61K39/001186 , A61K39/245 , A61P35/00 , C07K14/005 , C07K14/4738 , C07K14/4748 , C12N15/85 , A61K2039/5154 , A61K2039/53 , A61K2039/585 , C07K2319/01 , C07K2319/02 , C07K2319/06 , C07K2319/40 , C12N2710/16134 , C12N2800/22 , C12N2840/203
摘要: Vaccine design, polycistronic vaccine constructs, compositions, and methods comprising nucleic acids (DNA, RNA), peptides, proteins and derivatives thereof, including cells and cell-lines, for enhanced antigen-specific vaccination.
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公开(公告)号:US12102679B2
公开(公告)日:2024-10-01
申请号:US17897885
申请日:2022-08-29
发明人: Xiaoping Zhu , Xiaoyang Liu
IPC分类号: A61K39/245 , A61K38/16 , C12N7/00 , C12N15/113
CPC分类号: A61K39/245 , A61K38/162 , C12N7/00 , C12N15/1131 , C12N2710/16133
摘要: HCMV US11 based therapeutics that can be used to target and reduce the activity of the FcRn protein are provided. The compositions can be used in treatment of auto-immune mediated and albumin-mediated diseases in a subject HCMV US11, as well as for use in preventing, or treating, infections of HCMV through administration of a US11 inhibitor.
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公开(公告)号:US12098167B2
公开(公告)日:2024-09-24
申请号:US17762308
申请日:2020-12-15
发明人: Musheng Zeng , Cong Sun , Yixin Zeng , Guokai Feng , Yinfeng Kang , Xinchun Chen , Xiao Zhang , Qianying Zhu , Jiangping Li , Xiangwei Kong
IPC分类号: C07K14/05 , A61K9/51 , A61K39/00 , A61K39/245 , A61P31/22
CPC分类号: C07K14/05 , A61K9/51 , A61K39/245 , A61P31/22 , A61K2039/55555
摘要: The present invention is related to a self-assembled nanoparticle containing a gB protein of an EB virus and a preparation method and use thereof. The self-assembled nanoparticle comprises a first polypeptide and a second polypeptide; the first polypeptide comprises the gB protein and a first vector subunit, the second polypeptide comprises a second vector subunit; the first vector subunit is I53-50A1, and the second vector subunit is I53-50B.4PT1. In the self-assembled nanoparticle, the gB protein of the EB virus is displayed on the surface of the nanoparticle for the first time. The particle size of the self-assembled nanoparticle is larger than that of the antigen gB, and the chemical stability of the self-assembled nanoparticle is higher than that of the antigen gB, and the binding capacity with the neutralizing antibody of the self-assembled nanoparticle are higher than that of the antigen gB.
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公开(公告)号:US20240293535A1
公开(公告)日:2024-09-05
申请号:US18262033
申请日:2022-01-18
发明人: Johann MOLS , Marie TOUSSAINT
IPC分类号: A61K39/245 , A61P31/22 , C07K14/005
CPC分类号: A61K39/245 , A61P31/22 , C07K14/005 , C12N2710/16622 , C12N2710/16634
摘要: The present invention relates to a HSV2 Fc receptor or immunogenic fragment or variant thereof for use in generating a cross reactive immune response against HSV1 in a subject. Also provided is a HSV1 Fc receptor or immunogenic fragment or variant thereof for use in generating a cross reactive immune response against HSV2 when administered to a subject.
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公开(公告)号:US12054744B2
公开(公告)日:2024-08-06
申请号:US17224966
申请日:2021-04-07
IPC分类号: C12N5/0783 , A61K35/17 , A61K39/245 , A61K45/06 , A61P35/00 , C12N7/00 , A61K39/00
CPC分类号: C12N5/0646 , A61K35/17 , A61K39/245 , A61K45/06 , A61P35/00 , C12N7/00 , A61K2039/572 , A61K2039/585 , C12N2501/04 , C12N2501/2315 , C12N2501/2321 , C12N2501/42 , C12N2501/599 , C12N2502/1121 , C12N2502/1157 , C12N2502/1352 , C12N2710/16134
摘要: This disclosure describes an adaptive NK cell, an isolated population of adaptive Natural Killer (NK) cells, a composition including an adaptive NK cell, and methods for producing, preparing, and using an adaptive NK cell or an isolated population or composition including an adaptive NK cell. The adaptive NK cells may be used to treat a viral infection or a tumor.
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公开(公告)号:US20240248080A1
公开(公告)日:2024-07-25
申请号:US18629922
申请日:2024-04-08
IPC分类号: G01N33/50 , A61K39/00 , A61K39/245 , C07K14/005 , C12N7/00
CPC分类号: G01N33/5091 , A61K39/245 , C07K14/005 , C12N7/00 , A61K2039/5254 , A61K2039/80 , C12N2710/16022 , C12N2710/16052 , G01N2333/03
摘要: Kaposi's sarcoma-associated herpesvirus (KSHV) is an opportunistic pathogen causing Kaposi's sarcoma. It is capable of establishing latent infection, which can be reactivated to engage lytic infection for progeny production. KSHV contains a ˜165 kilobase DNA genome predicted to encode at least 90 open reading frames (ORFs). In this report, we generated 91 KSHV mutants, each characterized by the disruption of a single viral ORF. The growth of these mutants in cultured cells was examined to systematically investigate the necessity of each ORF for viral latency, reactivation, and lytic replication. Salient aspects are (a) 44 ORFs are essential for viral lytic replication in cultured cells and 47 are nonessential; (b) KSHV reactivation can be positively or negatively regulated by specific viral ORFs; and (c) ORFs identified to regulate viral reactivation encode functions modulating both innate and adaptive immune responses. The intersection of viral immunomodulatory genes controlling reactivation suggests that KSHV engages in a concerted effort to communicate and respond to the host immune system for reactivation and replication using a viral sensory network. Our results imply a novel mechanism in which reactivation of KSHV is actively controlled by the virus in response to its surrounding environment, leading to the opportunistic nature of viral diseases that are strongly correlated to the host's immune status and conditions.
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公开(公告)号:US20240199724A1
公开(公告)日:2024-06-20
申请号:US18272255
申请日:2022-01-28
申请人: THELPER AS
发明人: Katja Vetvik
CPC分类号: C07K16/089 , A61K39/245 , A61K47/68 , A61P31/22 , C07K14/70539 , C12N15/63 , A61K2039/505 , C07K2317/31 , C07K2317/55 , C07K2317/565 , C07K2317/569 , C07K2319/30
摘要: The present invention provides binding molecules having one or more of (preferably all of) highly specific binding to the US28 protein of human cytomegalovirus (HCMV), very low levels of non-specific binding to healthy (non-infected) cells, and/or a strain-agnostic binding ability, as well as nucleic acid molecules encoding the said binding molecules. The binding molecules are designed to bind to extracellular domain 3 (ECD3) of a US28 protein of human cytomegalovirus (HCMV), the third of the four extracellular domains presented by US28, corresponding to positions 167 to 183 of the US28 protein sequence as defined by SEQ ID NO:5. The binding molecules of the present invention have been demonstrated to have excellent binding properties, including particular binding specificity for aggressive and/or metastasizing HCMV-infected cancers, including breast cancers. In certain preferred embodiments, the binding molecule is selected from an antibody (including, for example, a BiTE antibody) and a chimeric antigen receptor (CAR), or functional variants, fragments, fusion proteins, and/or conjugates thereof. Also provided are cells expressing said binding molecules, such as CAR-expressing cells, including CAR-T cells, CAR-NK cells, and CAR-M cells.
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公开(公告)号:US12005102B2
公开(公告)日:2024-06-11
申请号:US17091553
申请日:2020-11-06
申请人: AC Immune SA
IPC分类号: A61K39/395 , A61K9/127 , A61K39/00 , A61K39/05 , A61K39/08 , A61K39/245 , A61K39/39 , A61P25/28 , C07K14/005
CPC分类号: A61K39/0007 , A61K9/127 , A61K39/0003 , A61K39/0005 , A61K39/05 , A61K39/08 , A61K39/245 , A61K39/39 , A61P25/28 , C07K14/005 , A61K2039/55516 , A61K2039/55555 , A61K2039/55572 , A61K2039/57 , A61K2039/575 , A61K2039/58 , A61K2039/627 , A61K2039/645 , A61K2039/70 , C07K2319/33 , C07K2319/55 , C12N2710/16232 , C12N2710/16234 , C12N2760/16033
摘要: A liposomal vaccine composition comprises a β-amyloid (Aβ)-derived peptide antigen displayed on the surface of the liposome. The vaccine composition also comprises a peptide comprising a universal T-cell epitope encapsulated within the liposome. The vaccine composition also comprises an adjuvant, which may form part of the liposome and may be displayed at least in part on the surface of the liposome. These vaccine compositions are used for treating, preventing, inducing a protective immune response against or alleviating the symptoms associated with an amyloid-beta associated disease or condition or a condition characterised by, or associated with, loss of cognitive memory capacity in a subject. The vaccine compositions may be provided as a kit. Related methods of producing a liposomal vaccine composition are also provided.
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公开(公告)号:US20240123057A1
公开(公告)日:2024-04-18
申请号:US18163038
申请日:2023-02-01
申请人: Intervet Inc.
发明人: Stephanie Cook , Mohamad Morsey , Ian Tarpey , Iwan Verstegen , Paulus Jacobus Antonius Sondermeijer , Paul Vermeij
IPC分类号: A61K39/245 , A61P31/22 , C12N7/00
CPC分类号: A61K39/245 , A61P31/22 , C12N7/00 , A61K2039/5256
摘要: The present invention discloses novel recombinant multivalent non-pathogenic Marek's Disease virus constructs that encode and express both Infectious Laryngotracheitis Virus protein antigens and an Infectious Bursal Disease virus protein antigen, and methods of their use in poultry vaccines.
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公开(公告)号:US11932669B2
公开(公告)日:2024-03-19
申请号:US17223207
申请日:2021-04-06
IPC分类号: C07K14/045 , A61K38/00 , A61K39/245
CPC分类号: C07K14/045 , A61K39/245 , A61K38/00
摘要: Described are mutant human cytomegalovirus (HCMV) pentamer complex polypeptides, methods of making them, and their use in HCMV protein complexes and compositions. In particular, the use of the modified HCMV polypeptides to stabilize HCMV complexes or unmask a pentamer epitope is described.
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