JPH11510685A5 - - Google Patents

Info

Publication number
JPH11510685A5
JPH11510685A5 JP1997501407A JP50140797A JPH11510685A5 JP H11510685 A5 JPH11510685 A5 JP H11510685A5 JP 1997501407 A JP1997501407 A JP 1997501407A JP 50140797 A JP50140797 A JP 50140797A JP H11510685 A5 JPH11510685 A5 JP H11510685A5
Authority
JP
Japan
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
JP1997501407A
Other languages
English (en)
Japanese (ja)
Other versions
JP4210798B2 (ja
Publication date
Priority claimed from US08/474,210 external-priority patent/US5993800A/en
Application filed filed Critical
Priority claimed from PCT/US1996/008974 external-priority patent/WO1996039514A1/en
Publication of JPH11510685A5 publication Critical patent/JPH11510685A5/ja
Application granted granted Critical
Publication of JP4210798B2 publication Critical patent/JP4210798B2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

JP50140797A 1995-06-05 1996-06-05 可溶性ctla4分子を用いる関心とする遺伝子の発現を延長する方法 Expired - Lifetime JP4210798B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US46840795A 1995-06-05 1995-06-05
US08/474,210 US5993800A (en) 1995-06-05 1995-06-06 Methods for prolonging the expression of a heterologous gene of interest using soluble CTLA4 molecules and an antiCD40 ligand
PCT/US1996/008974 WO1996039514A1 (en) 1995-06-05 1996-06-05 Method for prolonging the expression of a gene of interest using soluble ctla4 molecules

Publications (2)

Publication Number Publication Date
JPH11510685A5 true JPH11510685A5 (enExample) 2004-07-22
JP4210798B2 JP4210798B2 (ja) 2009-01-21

Family

ID=23859695

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50140797A Expired - Lifetime JP4210798B2 (ja) 1995-06-05 1996-06-05 可溶性ctla4分子を用いる関心とする遺伝子の発現を延長する方法

Country Status (2)

Country Link
US (1) US5993800A (enExample)
JP (1) JP4210798B2 (enExample)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6887471B1 (en) 1991-06-27 2005-05-03 Bristol-Myers Squibb Company Method to inhibit T cell interactions with soluble B7
WO1997013514A1 (en) * 1995-10-10 1997-04-17 Pfizer Inc. Nk-1 receptor antagonists for prevention of neurogenic inflammation in gene therapy
US20030219863A1 (en) * 1997-01-31 2003-11-27 Bristol-Myers Squibb Company Soluble CTLA4 mutant molecules and uses thereof
US7094874B2 (en) 2000-05-26 2006-08-22 Bristol-Myers Squibb Co. Soluble CTLA4 mutant molecules
CA2413190C (en) * 2000-07-03 2009-04-07 Bristol-Myers Squibb Company Methods for treating rheumatic diseases using a soluble ctla4 molecule
US20040022787A1 (en) 2000-07-03 2004-02-05 Robert Cohen Methods for treating an autoimmune disease using a soluble CTLA4 molecule and a DMARD or NSAID
HUP0303930A3 (en) * 2001-01-26 2012-09-28 Univ Emory Methods of inducing organ transplant tolerance and correcting hemoglobinopathies
ATE390931T1 (de) * 2001-05-23 2008-04-15 Bristol Myers Squibb Co Verfahren zum schützen eines allogenen inseltransplantats mit löslichen ctla4- mutationsmolekülen
US20030086903A1 (en) * 2001-11-02 2003-05-08 Genvec, Inc. Therapeutic regimen for treating cancer
CN1665533A (zh) * 2002-05-02 2005-09-07 康涅狄格大学健康中心 热激蛋白用于增强抗体疗法功效的用途
JP2007511507A (ja) * 2003-11-14 2007-05-10 ジェンベク、インコーポレイティッド 癌を処置するための治療レジメン
EP2007795B1 (en) 2006-03-30 2016-11-16 The Board Of Trustees Of The Leland Stanford Junior University Aav capsid proteins
US20090181078A1 (en) * 2006-09-26 2009-07-16 Infectious Disease Research Institute Vaccine composition containing synthetic adjuvant
US8273361B2 (en) 2006-09-26 2012-09-25 Infectious Disease Research Institute Vaccine composition containing synthetic adjuvant
DK2222697T3 (da) * 2007-11-01 2013-03-11 Perseid Therapeutics Llc Immunsuppressive polypeptider og nukleinsyrer
LT2437753T (lt) 2009-06-05 2016-12-12 Infectious Disease Research Institute Sintetiniai gliukopiranozillipidų adjuvantai ir juos turinčios vakcinų kompozicijos
US9605844B2 (en) * 2009-09-01 2017-03-28 Cree, Inc. Lighting device with heat dissipation elements
AU2011309689B2 (en) 2010-09-28 2015-01-15 Hadasit Medical Research Services & Development Ltd. Compositions and methods for treatment of hematological malignancies
WO2012141984A1 (en) 2011-04-08 2012-10-18 Immune Design Corp. Immunogenic compositions and methods of using the compositions for inducing humoral and cellular immune responses
US11510875B2 (en) 2012-02-07 2022-11-29 Access To Advanced Health Institute Adjuvant formulations comprising TLR4 agonists and methods of using the same
LT2850431T (lt) 2012-05-16 2018-06-25 Immune Design Corp. Vakcinos, skirtos hsv-2
KR102039520B1 (ko) 2013-04-18 2019-11-01 이뮨 디자인 코포레이션 암 치료에 이용하기 위한 gla 단일요법
US9463198B2 (en) 2013-06-04 2016-10-11 Infectious Disease Research Institute Compositions and methods for reducing or preventing metastasis
HUE059605T2 (hu) 2016-05-16 2022-11-28 Access To Advanced Health Inst TLR agonista tartalmú készítmény és használati eljárások
JP7140684B2 (ja) 2016-06-01 2022-09-21 アクセス ツー アドバンスト ヘルス インスティチュート サイジング剤含有ナノアラム粒子
CA3078223A1 (en) 2017-09-08 2019-03-14 Infectious Disease Research Institute Liposomal formulations comprising saponin and methods of use

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5693622A (en) * 1989-03-21 1997-12-02 Vical Incorporated Expression of exogenous polynucleotide sequences cardiac muscle of a mammal
US5399346A (en) * 1989-06-14 1995-03-21 The United States Of America As Represented By The Department Of Health And Human Services Gene therapy
US5770197A (en) * 1991-06-27 1998-06-23 Bristol-Myers Squibb Company Methods for regulating the immune response using B7 binding molecules and IL4-binding molecules
US5872154A (en) * 1995-02-24 1999-02-16 The Trustees Of The University Of Pennsylvania Method of reducing an immune response to a recombinant adenovirus

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