JP2007526318A5 - - Google Patents

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JP2007526318A5
JP2007526318A5 JP2007501899A JP2007501899A JP2007526318A5 JP 2007526318 A5 JP2007526318 A5 JP 2007526318A5 JP 2007501899 A JP2007501899 A JP 2007501899A JP 2007501899 A JP2007501899 A JP 2007501899A JP 2007526318 A5 JP2007526318 A5 JP 2007526318A5
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acid sequence
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Priority claimed from PCT/US2005/006588 external-priority patent/WO2005084306A2/en
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自己トランスポーター抗原として使用するためのポリペプチドであって、該ポリペプチドは、以下:
(a)配列番号54、配列番号6、配列番号55、配列番号56、配列番号78および配列番号79からなる群より選択されるアミノ酸配列、
(b)(a)のアミノ酸配列に対して少なくとも50%の配列同一性を有するアミノ酸配列;または
(c)(a)のアミノ酸配列からの少なくとも7個の連続したアミノ酸の1以上のフラグメントまたはこれらの組み合わせを含む、アミノ酸配列
を含む、ポリペプチド。
A polypeptide for use as a self-transporter antigen, the polypeptide comprising:
(A) an amino acid sequence selected from the group consisting of SEQ ID NO: 54, SEQ ID NO: 6, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 78, and SEQ ID NO: 79;
(B) an amino acid sequence having at least 50% sequence identity to the amino acid sequence of (a); or (c) one or more fragments of at least 7 consecutive amino acids from the amino acid sequence of (a) or these A polypeptide comprising an amino acid sequence comprising a combination of:
前記使用が、Chlamydia pneumoniae特異的な免疫応答を惹起させるための抗原としての使用である、請求項1に記載のポリペプチド。 2. The polypeptide according to claim 1, wherein the use is as an antigen to elicit a Chlamydia pneumoniae specific immune response. 前記使用が、Chlamydia pneumoniaeに感染した個体において全身性の免疫応答を惹起させるための使用である、請求項2に記載のポリペプチド。 3. The polypeptide of claim 2, wherein the use is for raising a systemic immune response in an individual infected with Chlamydia pneumoniae. V型の自己トランスポーター分泌系の機構を通して、宿主細胞の細胞質内へと分泌される、請求項1〜3のいずれか1項に記載のポリペプチド。 The polypeptide according to any one of claims 1 to 3, which is secreted into the cytoplasm of a host cell through a mechanism of a V-type autotransporter secretion system. 前記ポリペプチドが、配列番号54、配列番号6、配列番号55、配列番号56、配列番号78および配列番号79からなる群より選択され、そして、G、DG、VG、G、AV、G、IVG、GTLGG、S、IVG、およびMからなる群より選択される、1以上の一般的なN末端配列モチーフを共有する、請求項1〜3のいずれか1項に記載のポリペプチド。 The polypeptide is selected from the group consisting of SEQ ID NO: 54, SEQ ID NO: 6, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 78 and SEQ ID NO: 79, and G, DG, VG, G, AV, G, IVG The polypeptide of any one of claims 1 to 3, which shares one or more common N-terminal sequence motifs selected from the group consisting of GTLGG, S, IVG, and M. 前記一般的なN末端配列モチーフが、GTLGG、S、IVGおよびMからなる群より選択される、請求項5に記載のポリペプチド。 6. The polypeptide of claim 5, wherein the common N-terminal sequence motif is selected from the group consisting of GTLGG, S, IVG and M. 診断において使用するための、請求項1〜3のいずれか1項に記載のポリペプチド。 4. A polypeptide according to any one of claims 1 to 3 for use in diagnosis. 個体におけるChlamydia pneumoniae感染の予防または処置のための医薬の調製における、請求項1〜3のいずれか1項に記載のポリペプチドの使用。 Use of the polypeptide according to any one of claims 1 to 3 in the preparation of a medicament for the prevention or treatment of Chlamydia pneumoniae infection in an individual. 前記使用が、Chlamydia pneumoniaeに感染した個体のセロポジティブな血清と免疫反応する、自己トランスポータータンパク質を使用する、請求項8に記載の使用。 9. Use according to claim 8, wherein the use uses a self-transporter protein that immunoreacts with seropositive sera of individuals infected with Chlamydia pneumoniae. 個体におけるChlamydia pneumoniae感染の診断のためのアッセイの調製における、請求項1〜3のいずれか1項に記載のポリペプチドの使用。 Use of a polypeptide according to any one of claims 1 to 3 in the preparation of an assay for the diagnosis of Chlamydia pneumoniae infection in an individual. 個体において免疫応答を惹起させるための組成物であって、以下:
(a)配列番号54、配列番号6、配列番号55、配列番号56、配列番号78および配列番号79からなる群より選択されるアミノ酸配列、
(b)(a)のアミノ酸配列に対して少なくとも50%の配列同一性を有するアミノ酸配列、または
(c)(a)のアミノ酸配列からの少なくとも1、2、3、4、5、6もしくは7個のアミノ酸の1以上のフラグメントまたはこれらの混合物を含む、アミノ酸配列
を含むポリペプチドを含む組成物
A composition for eliciting an immune response in an individual, hereinafter:
(A) an amino acid sequence selected from the group consisting of SEQ ID NO: 54, SEQ ID NO: 6, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 78, and SEQ ID NO: 79;
(B) an amino acid sequence having at least 50% sequence identity to the amino acid sequence of (a), or (c) at least 1, 2, 3, 4, 5, 6 or 7 from the amino acid sequence of (a) comprising one or more fragments or mixtures of these pieces of amino acids, polypeptides comprising the amino acid sequence, composition.
個体における免疫応答を診断するための組成物であって、該組成物は、請求項1〜3のいずれか1項に記載のポリペプチドに結合する結合因子を含み、ここで該組成物は、該個体から得られた生物学的サンプルと接触させられ、該結合因子に結合するポリペプチドの量が検出され、そして該ポリペプチドの量が、該個体における免疫応答の存在を決定するために所定のカットオフ値と比較される組成物A composition for diagnosing an immune response in an individual, the composition comprising a binding agent that binds to a polypeptide according to any one of claims 1-3, wherein the composition, Contacted with a biological sample obtained from the individual, the amount of polypeptide binding to the binding agent is detected, and the amount of the polypeptide is predetermined to determine the presence of an immune response in the individual A composition that is compared to a cutoff value of . 前記ポリペプチドが、請求項1〜3のいずれか1項に記載される、請求項11または請求項12に記載の組成物13. A composition according to claim 11 or claim 12, wherein the polypeptide is described in any one of claims 1-3. 前記ポリペプチドが、請求項2〜6のいずれか1項に記載される、請求項11に記載の方法、または請求項8〜9のいずれか1項に記載の使用。 The method according to claim 11 or the use according to any one of claims 8 to 9, wherein the polypeptide is described in any one of claims 2-6. 1以上のChlamydia pneumoniae自己トランスポータータンパク質またはその免疫原性フラグメント、および、1以上の免疫賦活薬を含有する、免疫応答を惹起させるための組成物。 A composition for raising an immune response, comprising one or more Chlamydia pneumoniae self-transporter proteins or immunogenic fragments thereof and one or more immunostimulants. 請求項15に記載の組成物であって、前記Chlamydia pneumoniae自己トランスポータータンパク質もしくはその免疫原性フラグメントが、以下:
(a)配列番号54、配列番号6、配列番号55、配列番号56、配列番号78、配列番号86および配列番号79からなる群より選択されるアミノ酸配列;
(b)(a)のアミノ酸配列に対して少なくとも50%の配列同一性を有するアミノ酸配列;または
(c)(a)のアミノ酸配列からの少なくとも1、2、3、4、5、6もしくは7個のアミノ酸の1以上のフラグメントまたはこれらの組み合わせを含む、アミノ酸配列
を含む、組成物。
16. The composition of claim 15, wherein the Chlamydia pneumoniae self-transporter protein or immunogenic fragment thereof is:
(A) an amino acid sequence selected from the group consisting of SEQ ID NO: 54, SEQ ID NO: 6, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 78, SEQ ID NO: 86, and SEQ ID NO: 79;
(B) an amino acid sequence having at least 50% sequence identity to the amino acid sequence of (a); or (c) at least 1, 2, 3, 4, 5, 6 or 7 from the amino acid sequence of (a) A composition comprising an amino acid sequence comprising one or more fragments of amino acids or combinations thereof.
前記タンパク質またはその免疫原性フラグメントが、請求項1〜3のいずれか1項に記載される、請求項15または16に記載の組成物。 17. A composition according to claim 15 or 16, wherein the protein or immunogenic fragment thereof is described in any one of claims 1-3. 2以上のChlamydia pneumoniae自己トランスポータータンパク質またはその免疫原性フラグメントを含む、被験体において免疫応答を惹起させるための組成物。 A composition for raising an immune response in a subject, comprising two or more Chlamydia pneumoniae autotransporter proteins or immunogenic fragments thereof. 請求項18に記載の組成物であって、前記Chlamydia pneumoniae自己トランスポータータンパク質またはその免疫原性フラグメントが、以下:
(a)配列番号54、配列番号6、配列番号55、配列番号56、配列番号78、配列番号86および配列番号79からなる群より選択されるアミノ酸配列;
(b)(a)のアミノ酸配列に対して少なくとも50%の配列同一性を有するアミノ酸配列;または
(c)(a)のアミノ酸配列からの少なくとも1、2、3、4、5、6もしくは7個のアミノ酸の1以上のフラグメントまたはこれらの組み合わせを含む、アミノ酸配列
を含む、組成物。
19. The composition of claim 18, wherein the Chlamydia pneumoniae self-transporter protein or immunogenic fragment thereof is:
(A) an amino acid sequence selected from the group consisting of SEQ ID NO: 54, SEQ ID NO: 6, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 78, SEQ ID NO: 86, and SEQ ID NO: 79;
(B) an amino acid sequence having at least 50% sequence identity to the amino acid sequence of (a); or (c) at least 1, 2, 3, 4, 5, 6 or 7 from the amino acid sequence of (a) A composition comprising an amino acid sequence comprising one or more fragments of amino acids or combinations thereof.
請求項18または19に記載の組成物であって、該組成物は、さらに、1以上の免疫賦活薬を含む、組成物。 20. The composition of claim 18 or 19, wherein the composition further comprises one or more immunostimulants. 請求項15または16のいずれか1項に記載の組成物を作製する方法であって、該方法は、1以上のChlamydia pneumoniae自己トランスポータータンパク質またはその免疫原性フラグメントを、1以上の免疫賦活薬と混合する工程を包含する、方法。 17. A method of making a composition according to any one of claims 15 or 16, wherein the method comprises one or more Chlamydia pneumoniae self-transporter proteins or immunogenic fragments thereof and one or more immunostimulatory agents. A method comprising the step of mixing with. 請求項18または19に記載の組成物を作製する方法であって、該方法は、2以上のChlyamydia pneumoniae自己トランスポータータンパク質またはその免疫原性フラグメントを混合する工程を包含する、方法。 20. A method of making a composition according to claim 18 or 19, wherein the method comprises mixing two or more Chlyamidia pneumoniae autotransporter proteins or immunogenic fragments thereof. 請求項22に記載の方法であって、該方法は、前記Chlamydia pneumoniae自己トランスポータータンパク質または免疫原性フラグメントに、1以上の免疫賦活薬を加える工程を包含する、方法。 23. The method of claim 22, wherein the method comprises adding one or more immunostimulants to the Chlamydia pneumoniae autotransporter protein or immunogenic fragment. Cpn0794、Cpn0795、Cpn0796、Cpn0797、CPn0798およびCpn0799からなる群より選択されるChlamydia pneumoniae自己トランスポータータンパク質、またはその免疫原性フラグメントであって、該自己トランスポータータンパク質のアミノ酸モチーフは、IVG、A、LGGおよびSを含む、タンパク質。 A Chlamydia pneumoniae self-transporter protein selected from the group consisting of Cpn0794, Cpn0779, Cpn0796, Cpn0797, CPn0798 and Cpn0799, or an immunogenic fragment thereof, wherein the amino acid motif of the self-transporter protein is IVG, A, LGG And a protein comprising S. 前記繰返しアミノ酸モチーフが、IVG、A、LGGおよびSを含む、請求項24に記載の自己トランスポータータンパク質。 25. The self-transporter protein of claim 24, wherein the repeated amino acid motif comprises IVG, A, LGG and S. 自己トランスポーター抗原として使用するためのポリペプチドであって、該ポリペプチドは、配列番号86に対応するアミノ酸配列、配列番号86に対して少なくとも50%の配列同一性を有するアミノ酸配列、または、配列番号86の少なくとも7個の連続するアミノ酸の1以上のフラグメントを含むアミノ酸配列、を含む、ポリペプチド。 A polypeptide for use as a self-transporter antigen, said polypeptide comprising an amino acid sequence corresponding to SEQ ID NO: 86, an amino acid sequence having at least 50% sequence identity to SEQ ID NO: 86, or a sequence A polypeptide comprising an amino acid sequence comprising one or more fragments of at least 7 consecutive amino acids of number 86. 前記使用が、Chlamydia pneumoniae特異的な免疫応答を惹起させるための抗原としての使用である、請求項26に記載のポリペプチド。 27. The polypeptide of claim 26, wherein the use is as an antigen to elicit a Chlamydia pneumoniae specific immune response. 前記使用が、Chlamydia pneumoniaeに感染した個体における全身性の免疫応答を惹起させるための使用である、請求項2に記載のポリペプチド。 The polypeptide according to claim 2, wherein the use is for raising a systemic immune response in an individual infected with Chlamydia pneumoniae. 個体におけるChlamydia pneumoniae感染の予防または処置のための医薬の調製における、請求項26〜28のいずれか1項に記載のポリペプチドの使用。 29. Use of a polypeptide according to any one of claims 26 to 28 in the preparation of a medicament for the prevention or treatment of Chlamydia pneumoniae infection in an individual. 個体において免疫応答を惹起させるための組成物であって、配列番号86に対応するアミノ酸配列、配列番号86に対して少なくとも50%の配列同一性を有するアミノ酸配列、または、配列番号86の少なくとも7個の連続するアミノ酸の1以上のフラグメントを含むアミノ酸配列を含むポリペプチドを含む組成物A composition for eliciting an immune response in an individual, SEQ ID NO 86 in the amino acid sequence corresponding an amino acid sequence having at least 50% sequence identity to SEQ ID NO: 86, or at least the SEQ ID NO: 86 polypeptides comprising an amino acid sequence comprising seven one or more fragments of consecutive amino acids, the composition. 個体における免疫応答を診断するための組成物であって、該組成物は、請求項26〜28のいずれか1項に記載のポリペプチドに結合する結合因子を含み、ここで該組成物は該個体から得られた生物学的サンプルと接触させられ、該結合因子に結合するポリペプチドの量は、該生物学的サンプルにおいて検出され、そして該ポリペプチドの量は、該個体における免疫応答の存在を決定するために、所定のカットオフ値と比較される、組成物A composition for diagnosing an immune response in an individual, the composition comprising a binding agent that binds to a polypeptide according to any one of claims 26 to 28, wherein the composition, The amount of polypeptide that is contacted with the biological sample obtained from the individual and that binds to the binding agent is detected in the biological sample , and the amount of polypeptide is a measure of the immune response in the individual. to determine the presence, Ru is compared with a predetermined cutoff value, composition.
JP2007501899A 2004-03-02 2005-03-02 Immunogenic composition against Chlamydiapneumoniae Withdrawn JP2007526318A (en)

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US54983204P 2004-03-02 2004-03-02
US64311005P 2005-01-12 2005-01-12
US64455205P 2005-01-19 2005-01-19
PCT/US2005/006588 WO2005084306A2 (en) 2004-03-02 2005-03-02 Immunogenic compositions for chlamydia pneunomiae

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EP2064230A2 (en) 2006-08-16 2009-06-03 Novartis AG Immunogens from uropathogenic escherichia coli
CA2731854C (en) * 2008-07-25 2020-06-30 Cellestis Limited Measurement of cell-mediated immune response reactivity to detect or monitor a disease or condition
WO2010032138A2 (en) 2008-09-18 2010-03-25 Novartis Ag Vaccine adjuvant combinations
ITMI20090946A1 (en) 2009-05-28 2010-11-29 Novartis Ag EXPRESSION OF RECOMBINANT PROTEINS
CN102740882A (en) 2009-08-27 2012-10-17 诺华有限公司 Adjuvant comprising aluminium, oligonucleotide and polycation
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CN102933267B (en) 2010-05-28 2015-05-27 泰特里斯在线公司 Interactive hybrid asynchronous computer game infrastructure
ES2458355T3 (en) 2010-09-01 2014-05-05 Novartis Ag Adsorption of immunopotentiators on insoluble metal salts
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RU2013144207A (en) 2011-03-02 2015-04-10 Новартис Аг COMBINED VACCINES WITH REDUCED DOSES OF ANTIGEN AND / OR ADJUVANT
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CA2866406A1 (en) 2012-03-08 2013-09-12 Novartis Ag Adjuvanted formulations of booster vaccines
JP6990522B2 (en) * 2017-04-11 2022-02-03 シスメックス株式会社 A method for measuring the immune stimulus response of immune cells, a method for determining the ability of immunological synapses to form in immune cells, and a cell analyzer.

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