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公开(公告)号:EP2170944A1
公开(公告)日:2010-04-07
申请号:EP08775781.1
申请日:2008-06-27
申请人: KINGS COLLEGE LONDON
CPC分类号: C07K14/62 , A61K38/00 , C07K7/06 , G01N33/505 , G01N33/6893 , G01N2800/042
摘要: The present invention provides isolated preproinsulin-derived peptides of 8 or 9 amino acids, comprising the amino acid sequence WGPDPAA (SEQ ID NO: 1), isolated Class I peptide-HLA complexes presenting said peptides and isolated molecules having binding affinity for said peptides and/or said peptide-HLA complexes. Such compositions are useful in the treatment of Type 1 diabetes mellitus (TlDM)
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公开(公告)号:EP4031161A1
公开(公告)日:2022-07-27
申请号:EP20780278.6
申请日:2020-09-16
申请人: Kings College London
发明人: PEAKMAN, Mark , VERHAGEN, Johan , EICHMANN, Martin
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公开(公告)号:EP3307298A1
公开(公告)日:2018-04-18
申请号:EP16729347.1
申请日:2016-06-10
申请人: Kings College London
发明人: PEAKMAN, Mark
摘要: The invention relates to a specific peptide combination. The peptide combination may be present in a pharmaceutically acceptable composition. The peptide combination can be used in the therapy or prevention of Type 1 Diabetes (TID). The invention also relates to a method of diagnosing or determining treatment efficacy, the method utilising the specific peptide combination.
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公开(公告)号:EP2170944B1
公开(公告)日:2014-04-09
申请号:EP08775781.1
申请日:2008-06-27
申请人: KINGS COLLEGE LONDON
CPC分类号: C07K14/62 , A61K38/00 , C07K7/06 , G01N33/505 , G01N33/6893 , G01N2800/042
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公开(公告)号:EP3307298B1
公开(公告)日:2020-01-15
申请号:EP16729347.1
申请日:2016-06-10
申请人: Kings College London
发明人: PEAKMAN, Mark
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公开(公告)号:EP1709070A1
公开(公告)日:2006-10-11
申请号:EP05701998.6
申请日:2005-01-24
申请人: KINGS COLLEGE LONDON
发明人: PEAKMAN, Mark
CPC分类号: C07K14/4713 , A61K38/00 , C07K14/62
摘要: Peptides for use in the therapy or prevention of Type 1 Diabetes mellitus (TIDM) are those having sequences containing QPLALEGSLQK (SEQ ID NO: 9). j Examples are those having a sequence selected from the group consisting 10 essentially of GGGPGAGSLQPLALEGSLQK (SEQ ID NO: 4), GSLQPLALEGSLQKRGIV (SEQ ID NO: 5), and QPLALEGSLQKRGIVEQ (SEQ ID NO: 6). One or more of the above peptides may be combined with one or more peptides having a sequence or sequences consisting essentially of sequences selected from LAKEWQALCAYQAEPNTCATAQGI?GNIK (SEQ ID NO: 11), KLKVESSPSRSDYINASPIIEHDP (SEQ ID NO: 12), and SFYLKNVQTQETRTLTQFHF (SEQ ID NO: 13). Also disclosed is a method of assessing the potential of a peptide for TIDM therapy or prevention which comprises subjecting the candidate peptide to a frst assay indicative of a pathogenic T cell response in blood or other biological sample, such as an ELISPOT assay for IFN-y. In the case of a positive response to the first assay, the candidate peptide is subjected to a second assay indicative of a regulatory T cell response to the peptide, such as an ELISPOT assay for IL 10).
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