JP2008526764A5 - - Google Patents

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Publication number
JP2008526764A5
JP2008526764A5 JP2007549646A JP2007549646A JP2008526764A5 JP 2008526764 A5 JP2008526764 A5 JP 2008526764A5 JP 2007549646 A JP2007549646 A JP 2007549646A JP 2007549646 A JP2007549646 A JP 2007549646A JP 2008526764 A5 JP2008526764 A5 JP 2008526764A5
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JP
Japan
Prior art keywords
primary
epitope
mhc
immunogen
antigen
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2007549646A
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English (en)
Japanese (ja)
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JP2008526764A (ja
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Publication date
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Priority claimed from PCT/US2005/047442 external-priority patent/WO2006071990A2/en
Publication of JP2008526764A publication Critical patent/JP2008526764A/ja
Publication of JP2008526764A5 publication Critical patent/JP2008526764A5/ja
Pending legal-status Critical Current

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JP2007549646A 2004-12-29 2005-12-29 免疫応答の誘導におけるcd4+細胞の回避方法 Pending JP2008526764A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US64082104P 2004-12-29 2004-12-29
PCT/US2005/047442 WO2006071990A2 (en) 2004-12-29 2005-12-29 Methods to bypass cd+4 cells in the induction of an immune response

Publications (2)

Publication Number Publication Date
JP2008526764A JP2008526764A (ja) 2008-07-24
JP2008526764A5 true JP2008526764A5 (enExample) 2009-02-26

Family

ID=36615526

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007549646A Pending JP2008526764A (ja) 2004-12-29 2005-12-29 免疫応答の誘導におけるcd4+細胞の回避方法

Country Status (9)

Country Link
US (1) US8703142B2 (enExample)
EP (1) EP1838342A2 (enExample)
JP (1) JP2008526764A (enExample)
AU (1) AU2005321905A1 (enExample)
CA (1) CA2592972A1 (enExample)
IL (1) IL184276A0 (enExample)
MX (1) MX2007008010A (enExample)
SG (1) SG158155A1 (enExample)
WO (1) WO2006071990A2 (enExample)

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EP2385059A3 (en) * 2005-06-17 2012-02-15 Mannkind Corporation Methods and compositions to elicit multivalent immune responses against dominant and subdominant epitopes, expressed on cancer cells and tumor stroma
US7511118B2 (en) 2005-06-17 2009-03-31 Mannkind Corporation PSMA peptide analogues
DE102005046490A1 (de) 2005-09-28 2007-03-29 Johannes-Gutenberg-Universität Mainz Modifikationen von RNA, die zu einer erhöhten Transkriptstabilität und Translationseffizienz führen
EP2023952B1 (en) 2006-05-18 2015-07-15 Epimmune Inc. Inducing immune responses to influenza virus using polypeptide and nucleic acid compositions
EP2046344A2 (en) * 2006-07-14 2009-04-15 MannKind Corporation Methods to elicit, enhance and sustain immune responses against mhc class-i restricted epitopes, for prophylactic or therapeutic purposes
CN101657213B (zh) * 2007-02-15 2014-02-26 曼康公司 用于增强t细胞应答的方法
EP2155782A2 (en) 2007-03-26 2010-02-24 Dako Denmark A/S Mhc peptide complexes and uses thereof in infectious diseases
EP2152890A1 (en) * 2007-05-23 2010-02-17 MannKind Corporation Multicistronic vectors and methods for their design
WO2009003493A2 (en) 2007-07-03 2009-01-08 Dako Denmark A/S Mhc multimers, methods for their generation, labeling and use
WO2009039854A2 (en) 2007-09-27 2009-04-02 Dako Denmark A/S Mhc multimers in tuberculosis diagnostics, vaccine and therapeutics
DK2254592T3 (da) 2008-02-28 2019-09-09 Dako Denmark As MHC-multimerer til Borrelia-diagnostik og sygdom
WO2010009735A2 (en) 2008-07-23 2010-01-28 Dako Denmark A/S Combinatorial analysis and repair
GB0817244D0 (en) 2008-09-20 2008-10-29 Univ Cardiff Use of a protein kinase inhibitor to detect immune cells, such as T cells
WO2010037402A1 (en) 2008-10-02 2010-04-08 Dako Denmark A/S Molecular vaccines for infectious disease
US11992518B2 (en) 2008-10-02 2024-05-28 Agilent Technologies, Inc. Molecular vaccines for infectious disease
US20110195090A1 (en) * 2008-10-11 2011-08-11 The United States Of America, As Represented By The Secretary, Department Of Health And Human Method of making a vaccine
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LT2714071T (lt) 2011-05-24 2019-10-10 Biontech Rna Pharmaceuticals Gmbh Individualizuotos vakcinos nuo vėžio
WO2013143555A1 (en) 2012-03-26 2013-10-03 Biontech Ag Rna formulation for immunotherapy
AU2013351542B2 (en) 2012-11-28 2018-08-09 BioNTech SE Individualized vaccines for cancer
WO2014180490A1 (en) 2013-05-10 2014-11-13 Biontech Ag Predicting immunogenicity of t cell epitopes
WO2015199617A1 (en) * 2014-06-24 2015-12-30 National University Of Singapore A monoclonal antibody with t-cell receptor-like specificity that targets epstein-barr infected human tumour cells based on their expression of ebna1
WO2016045732A1 (en) 2014-09-25 2016-03-31 Biontech Rna Pharmaceuticals Gmbh Stable formulations of lipids and liposomes
WO2016128060A1 (en) 2015-02-12 2016-08-18 Biontech Ag Predicting t cell epitopes useful for vaccination
TW201702272A (zh) * 2015-05-22 2017-01-16 美國紀念斯隆 凱特琳癌症中心 Prame肽專一性類t細胞受體抗體
WO2017059902A1 (en) 2015-10-07 2017-04-13 Biontech Rna Pharmaceuticals Gmbh 3' utr sequences for stabilization of rna
WO2018224166A1 (en) 2017-06-09 2018-12-13 Biontech Rna Pharmaceuticals Gmbh Methods for predicting the usefulness of disease specific amino acid modifications for immunotherapy
WO2020127222A2 (en) 2018-12-17 2020-06-25 Immudex Aps Panel comprising borrelia mhc multimers

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WO2006071989A2 (en) 2004-12-29 2006-07-06 Mannkind Corporation Methods to elicit, enhance and sustain immune responses against mhc class i-restricted epitopes, for prophylactic or therapeutic purposes
AU2005321898B2 (en) 2004-12-29 2012-07-19 Mannkind Corporation Use of compositions comprising various tumor-associated antigens as anti-cancer vaccines
EP2385059A3 (en) 2005-06-17 2012-02-15 Mannkind Corporation Methods and compositions to elicit multivalent immune responses against dominant and subdominant epitopes, expressed on cancer cells and tumor stroma
US7511118B2 (en) 2005-06-17 2009-03-31 Mannkind Corporation PSMA peptide analogues
NZ587601A (en) 2005-06-17 2012-05-25 Mannkind Corp Multivalent Entrain-and-Amplify Immunotherapeutics for Carcinoma
EP2046344A2 (en) 2006-07-14 2009-04-15 MannKind Corporation Methods to elicit, enhance and sustain immune responses against mhc class-i restricted epitopes, for prophylactic or therapeutic purposes

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