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公开(公告)号:US20190178871A1
公开(公告)日:2019-06-13
申请号:US16301019
申请日:2017-05-10
申请人: BioNTech RNA Pharmaceuticals GmbH , TRO-Translationable Onkologie an der Unversitatsme dizin der Johannes Gutenberg-Universitat Mainz
发明人: Mathias Vormehr , Ugur Sahin , Barbara Schrörs , Martin Löwer , Sebastian Boegel
摘要: The present invention relates to methods for predicting peptides or polypeptides such as T cell epitopes useful for immunotherapy such as for vaccination. In particular, the present invention relates to methods for predicting whether peptides or polypeptides such as tumor-associated antigens or epitopes, in particular tumor-associated neoantigens or neoepitopes, are immunogenic and, in particular, useful for immunotherapy such as for vaccination. The methods of the invention may be used, in particular, for the provision of vaccines which are specific for a patient's tumor and, thus, in the context of personalized cancer vaccines.
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公开(公告)号:US11156617B2
公开(公告)日:2021-10-26
申请号:US15550286
申请日:2016-02-09
申请人: BioNTech RNA Pharmaceuticals GmbH , TRON-Translationale Onkologie an der Universitätsmedizin der Johannes Gutenberg-Universität Mainz gGmbH
发明人: Ugur Sahin , Martin Löwer , Arbel D. Tadmor , Sebastian Boegel , Barbara Schrörs , Mathias Vormehr , Sebastian Kreiter
摘要: The present invention relates to methods for predicting T cell epitopes useful for vaccination. In particular, the present invention relates to methods for predicting whether modifications in peptides or polypeptides such as tumor-associated neoantigens are immunogenic and, in particular, useful for vaccination, or for predicting which of such modifications are most immunogenic and, in particular, most useful for vaccination. The methods of the invention may be used, in particular, for the provision of vaccines which are specific for a patient's tumor and thus, in the context of personalized cancer vaccines.
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公开(公告)号:US20210290746A1
公开(公告)日:2021-09-23
申请号:US17262180
申请日:2019-07-23
申请人: BioNTech RNA Pharmaceuticals GmbH , TRON - Translationale Onkologie an der Universitätsmedizin der Johannes Gutenberg-Universität Mainz
发明人: Ugur Sahin , Mathias Vormehr , Thomas Bukur
IPC分类号: A61K39/00 , C12Q1/6886 , A61P35/00
摘要: The present invention is in the field of tumor immunotherapy. In particular, the present invention provides individualized cancer vaccines specific for a patients tumor based on a transcriptome analysis in a tumor specimen of the patient for RNA transcripts which are excessively upregulated in one or more cancer cells of said patient. These individualized cancer vaccines when administered to the patient induce an immune response against tumor-associated antigens expressed in a tumor of the patient by the RNA transcripts which are excessively upregulated in one or more cancer cells of said patient. Due to the excessive upregulation of the RNA transcripts, the individualized cancer vaccines are effective for vaccination of a subject and for breaking the self-tolerance against tumor-associated antigens which are self-proteins in said subject.
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公开(公告)号:US20220074948A1
公开(公告)日:2022-03-10
申请号:US17481243
申请日:2021-09-21
申请人: BioNTech RNA Pharmaceuticals GmbH , TRON-Translationale Onkologie an der Universitätsmedizin der Johannes Gutenberg-
发明人: Ugur Sahin , Martin Löwer , Arbel D. Tadmor , Sebastian Boegel , Barbara Schrörs , Mathias Vormehr , Sebastian Kreiter
摘要: The present invention relates to methods for predicting T cell epitopes useful for vaccination. In particular, the present invention relates to methods for predicting whether modifications in peptides or polypeptides such as tumor-associated neoantigens are immunogenic and, in particular, useful for vaccination, or for predicting which of such modifications are most immunogenic and, in particular, most useful for vaccination. The methods of the invention may be used, in particular, for the provision of vaccines which are specific for a patient's tumor and thus, in the context of personalized cancer vaccines.
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公开(公告)号:US20210292386A1
公开(公告)日:2021-09-23
申请号:US17262097
申请日:2019-07-19
申请人: BioNTech RNA Pharmaceuticals GmbH , TRON - Translationale Onkologie an der Universitätsmedizin Der Johannes Gutenberg-Universität Mainz
发明人: Ugur Sahin , Mathias Vormehr , Lena Mareen Kranz , Sina Fellermeier-Kopf , Alexander Muik , Friederike Gieseke , Bodo Tillmann , Sonja Witzel
摘要: The invention relates to variants of interleukin-2 (IL2). In one embodiment, the IL2 variants activate effector T cells over regulatory T cells. In particular, the invention relates to a polypeptide comprising a mutein of human IL2 or of a functional variant of human IL2, wherein the human IL2 or functional variant thereof is substituted at at least a position having an acidic or basic amino acid residue in wild type human IL2 that contacts the alpha subunit of the αβγ IL2 receptor complex (I12Kαβγ). Alternatively, the mutein of human IL2 or of a functional variant of human IL2 comprises at least (i) one or more amino acid substitutions which reduce the affinity for the alpha subunit of II_2Kαβγ and (ii) one or more amino acid substitutions which enhance the affinity for II_2Kβγ. The invention also relates to polynucleotides coding for the polypeptides of the invention, host cells comprising the polynucleotides, pharmaceutical compositions comprising the polypeptides, polynucleotides or host cells, therapeutic or prophylactic methods of treatment using the polypeptides, polynucleotides, host cells or pharmaceutical compositions and medical preparations comprising the polypeptides, polynucleotides, host cells or pharmaceutical compositions.
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公开(公告)号:US20210113606A1
公开(公告)日:2021-04-22
申请号:US16966422
申请日:2019-02-08
申请人: BioNTech RNA Pharmaceuticals GmbH , TRON - Translationale Onkologie An Der Universitätsmedizin Der Johannes Gutenberg-Universität Mainz
发明人: Ugur Sahin , Lena Kranz , Mathias Vormehr , Mustafa Diken , Sebastian Kreiter , Bodo Tillmann
IPC分类号: A61K31/7105 , C07K14/55 , C07K14/54 , A61K39/00
摘要: The present disclosure relates to methods and compositions for inducing an immune response in a subject comprising co-administering to the subject RNA encoding peptides or proteins used for vaccination and RNA encoding IL-2 attached to a pharmacokinetic modifying group and/or RNA encoding IL-7 attached to a pharmacokinetic modifying group. The vaccine is particularly effective if an immune checkpoint inhibitor such as an anti-PD-L1 antibody is further administered. The present disclosure further relates to methods involving the target-specific delivery of a cytokine to a target organ or target tissue.
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