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公开(公告)号:US06753417B2
公开(公告)日:2004-06-22
申请号:US09952267
申请日:2001-09-12
申请人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
发明人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
IPC分类号: C07H2104
CPC分类号: C07K14/212 , A61K39/00 , C07K16/1217
摘要: The present invention discloses the existence of two novel proteins UspA1 and UspA2, and their respective genes uspA1 and uspA2. Each protein encompasses a region that is conserved between the two proteins and comprises an epitope that is recognized by the MAb 17C7. One or more than one of these species may aggregate to form the very high molecular weight form (i.e. greater than 200 kDa) of the UspA antigen. Compositions and both diagnostic and therapeutic methods for the treatment and study of M. catarrhalis are disclosed.
摘要翻译: 本发明公开了两种新型蛋白质UspA1和UspA2及其各自的基因uspA1和uspA2的存在。 每个蛋白质包含在两种蛋白质之间保守的区域,并且包含由MAb 17C7识别的表位。 这些物质中的一种或多于一种可能聚集形成UspA抗原的非常高分子量形式(即大于200kDa)。 公开了组合物以及用于治疗和研究卡他莫拉菌的诊断和治疗方法。
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公开(公告)号:US06310190B1
公开(公告)日:2001-10-30
申请号:US09336447
申请日:1999-06-21
申请人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
发明人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
IPC分类号: C07H2104
CPC分类号: C07K14/212 , A61K39/00 , C07K16/1217
摘要: The present invention discloses the existence of two novel proteins UspA1 and UspA2, and their respective genes uspA1 and uspA2. Each protein encompasses a region that is conserved between the two proteins and comprises an epitope that is recognized by the MAb 17C7. One or more than one of these species may aggregate to form the very high molecular weight form (i.e. greater than 200 kDa) of the UspA antigen. Compositions and both diagnostic and therapeutic methods for the treatment and study of M. catarrhalis are disclosed.
摘要翻译: 本发明公开了两种新型蛋白质UspA1和UspA2及其各自的基因uspA1和uspA2的存在。 每个蛋白质包含在两种蛋白质之间保守的区域,并且包含由MAb 17C7识别的表位。 这些物质中的一种或多于一种可能聚集形成UspA抗原的非常高分子量形式(即大于200kDa)。 公开了组合物以及用于治疗和研究卡他莫拉菌的诊断和治疗方法。
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公开(公告)号:US07344724B2
公开(公告)日:2008-03-18
申请号:US10872769
申请日:2004-06-21
申请人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
发明人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
IPC分类号: A61K39/02
CPC分类号: C07K14/212 , A61K39/00 , C07K16/1217
摘要: The present invention discloses the existence of two novel proteins UspA1 and UspA2, and their respective genes uspA1 and uspA2. Each protein encompasses a region that is conserved between the two proteins and comprises an epitope that is recognized by the MAb 17C7. One or more than one of these species may aggregate to form the very high molecular weight form (i.e. greater than 200 kDa) of the UspA antigen. Compositions and both diagnostic and therapeutic methods for the treatment and study of M. catarrhalis are disclosed.
摘要翻译: 本发明公开了两种新型蛋白质UspA1和UspA2及其各自的基因uspA1和uspA2的存在。 每个蛋白质包含在两种蛋白质之间保守的区域,并且包含由MAb 17C7识别的表位。 这些物质中的一种或多于一种可以聚集形成UspA抗原的非常高分子量形式(即大于200kDa)。 公开了组合物以及用于治疗和研究卡他莫拉菌的诊断和治疗方法。
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公开(公告)号:US07288646B2
公开(公告)日:2007-10-30
申请号:US10872768
申请日:2004-06-21
申请人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
发明人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
IPC分类号: C07H21/04
CPC分类号: C07K14/212 , A61K39/00 , C07K16/1217
摘要: The present invention discloses the existence of two novel proteins UspA1 and UspA2, and their respective genes uspA1 and uspA2. Each protein encompasses a region that is conserved between the two proteins and comprises an epitope that is recognized by the MAb 17C7. One or more than one of these species may aggregate to form the very high molecular weight form (ie. greater than 200 kDa) of the UspA antigen. Compositions and both diagnostic and therapeutic methods for the treatment and study of M catarrhalis are disclosed.
摘要翻译: 本发明公开了两种新型蛋白质UspA1和UspA2及其各自的基因uspA1和uspA2的存在。 每个蛋白质包含在两种蛋白质之间保守的区域,并且包含由MAb 17C7识别的表位。 这些物质中的一种或多于一种可能聚集形成UspA抗原的非常高分子量形式(即大于200kDa)。 公开了治疗和研究卡他莫拉胶囊的组合物和诊断和治疗方法。
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公开(公告)号:US07569683B2
公开(公告)日:2009-08-04
申请号:US12044818
申请日:2008-03-07
申请人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
发明人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
IPC分类号: C07H21/04
CPC分类号: C07K14/212 , A61K39/00 , C07K16/1217
摘要: The present invention discloses the existence of two novel proteins UspA1 and UspA2, and their respective genes uspA1 and uspA2. Each protein encompasses a region that is conserved between the two proteins and comprises an epitope that is recognized by the MAb 17C7. One or more than one of these species may aggregate to form the very high molecular weight form (i.e. greater than 200 kDa) of the UspA antigen. Compositions and both diagnostic and therapeutic methods for the treatment and study of M. catarrhalis are disclosed.
摘要翻译: 本发明公开了两种新型蛋白质UspA1和UspA2及其各自的基因uspA1和uspA2的存在。 每个蛋白质包含在两种蛋白质之间保守的区域,并且包含由MAb 17C7识别的表位。 这些物质中的一种或多于一种可能聚集形成UspA抗原的非常高分子量形式(即大于200kDa)。 公开了组合物以及用于治疗和研究卡他莫拉菌的诊断和治疗方法。
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公开(公告)号:US20090118486A1
公开(公告)日:2009-05-07
申请号:US12044805
申请日:2008-03-07
申请人: ERIC J. HANSEN , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
发明人: ERIC J. HANSEN , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
IPC分类号: C07H21/00
CPC分类号: C07K14/212 , A61K39/00 , C07K16/1217
摘要: The present invention discloses the existence of two novel proteins UspA1 and UspA2, and their respective genes uspA1 and uspA2. Each protein encompasses a region that is conserved between the two proteins and comprises an epitope that is recognized by the MAb 17C7. One or more than one of these species may aggregate to form the very high molecular weight form (i.e. greater than 200 kDa) of the UspA antigen. Compositions and both diagnostic and therapeutic methods for the treatment and study of M. catarrhalis are disclosed.
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公开(公告)号:US07576194B2
公开(公告)日:2009-08-18
申请号:US12044805
申请日:2008-03-07
申请人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
发明人: Eric J. Hansen , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
IPC分类号: C07H21/04
CPC分类号: C07K14/212 , A61K39/00 , C07K16/1217
摘要: The present invention discloses the existence of two novel proteins UspA1 and UspA2, and their respective genes uspA1 and uspA2. Each protein encompasses a region that is conserved between the two proteins and comprises an epitope that is recognized by the MAb 17C7. One or more than one of these species may aggregate to form the very high molecular weight form (i.e. greater than 200 kDa) of the UspA antigen. Compositions and both diagnostic and therapeutic methods for the treatment and study of M. catarrhalis are disclosed.
摘要翻译: 本发明公开了两种新型蛋白质UspA1和UspA2及其各自的基因uspA1和uspA2的存在。 每个蛋白质包含在两种蛋白质之间保守的区域,并且包含由MAb 17C7识别的表位。 这些物质中的一种或多于一种可能聚集形成UspA抗原的非常高分子量形式(即大于200kDa)。 公开了组合物以及用于治疗和研究卡他莫拉菌的诊断和治疗方法。
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8.
公开(公告)号:US20090137788A1
公开(公告)日:2009-05-28
申请号:US12044818
申请日:2008-03-07
申请人: ERIC J. HANSEN , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
发明人: ERIC J. HANSEN , Christoph Aebi , Leslie D. Cope , Isobel Maciver , Michael J. Fiske , Ross A. Fredenburg
IPC分类号: C07H21/00
CPC分类号: C07K14/212 , A61K39/00 , C07K16/1217
摘要: The present invention discloses the existence of two novel proteins UspA1 and UspA2, and their respective genes uspA1 and uspA2. Each protein encompasses a region that is conserved between the two proteins and comprises an epitope that is recognized by the MAb 17C7. One or more than one of these species may aggregate to form the very high molecular weight form (i.e. greater than 200 kDa) of the UspA antigen. Compositions and both diagnostic and therapeutic methods for the treatment and study of M. catarrhalis are disclosed.
摘要翻译: 本发明公开了两种新型蛋白质UspA1和UspA2及其各自的基因uspA1和uspA2的存在。 每个蛋白质包含在两种蛋白质之间保守的区域,并且包含由MAb 17C7识别的表位。 这些物质中的一种或多于一种可能聚集形成UspA抗原的非常高分子量形式(即大于200kDa)。 公开了组合物以及用于治疗和研究卡他莫拉菌的诊断和治疗方法。
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