JP2014530603A5 - - Google Patents

Download PDF

Info

Publication number
JP2014530603A5
JP2014530603A5 JP2014534726A JP2014534726A JP2014530603A5 JP 2014530603 A5 JP2014530603 A5 JP 2014530603A5 JP 2014534726 A JP2014534726 A JP 2014534726A JP 2014534726 A JP2014534726 A JP 2014534726A JP 2014530603 A5 JP2014530603 A5 JP 2014530603A5
Authority
JP
Japan
Prior art keywords
vivo method
hiv
cells
endogenous
transgene
Prior art date
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
JP2014534726A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014530603A (ja
Filing date
Publication date
Application filed filed Critical
Publication of JP2014530603A publication Critical patent/JP2014530603A/ja
Publication of JP2014530603A5 publication Critical patent/JP2014530603A5/ja
Pending legal-status Critical Current

Links

JP2014534726A 2011-10-06 2012-10-04 Hiv感染を制御するための方法および組成物 Pending JP2014530603A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161544101P 2011-10-06 2011-10-06
US61/544,101 2011-10-06

Publications (2)

Publication Number Publication Date
JP2014530603A JP2014530603A (ja) 2014-11-20
JP2014530603A5 true JP2014530603A5 (https=) 2015-10-08

Family

ID=48044158

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014534726A Pending JP2014530603A (ja) 2011-10-06 2012-10-04 Hiv感染を制御するための方法および組成物

Country Status (7)

Country Link
US (2) US20130171732A1 (https=)
EP (1) EP2764102A4 (https=)
JP (1) JP2014530603A (https=)
AU (1) AU2012318562A1 (https=)
CA (1) CA2849920A1 (https=)
HK (1) HK1200491A1 (https=)
WO (1) WO2013052681A1 (https=)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6188703B2 (ja) * 2011-10-27 2017-08-30 サンガモ セラピューティクス, インコーポレイテッド Hprt遺伝子座を修飾するための方法および組成物
DK2931897T3 (en) 2012-12-12 2018-02-05 Broad Inst Inc CONSTRUCTION, MODIFICATION AND OPTIMIZATION OF SYSTEMS, PROCEDURES AND COMPOSITIONS FOR SEQUENCE MANIPULATION AND THERAPEUTICAL APPLICATIONS
WO2014093709A1 (en) 2012-12-12 2014-06-19 The Broad Institute, Inc. Methods, models, systems, and apparatus for identifying target sequences for cas enzymes or crispr-cas systems for target sequences and conveying results thereof
EP2931899A1 (en) 2012-12-12 2015-10-21 The Broad Institute, Inc. Functional genomics using crispr-cas systems, compositions, methods, knock out libraries and applications thereof
WO2014204724A1 (en) 2013-06-17 2014-12-24 The Broad Institute Inc. Delivery, engineering and optimization of tandem guide systems, methods and compositions for sequence manipulation
MX2015017312A (es) 2013-06-17 2017-04-10 Broad Inst Inc Suministro y uso de composiciones, vectores y sistemas crispr-cas para la modificación dirigida y terapia hepáticas.
EP3725885A1 (en) 2013-06-17 2020-10-21 The Broad Institute, Inc. Functional genomics using crispr-cas systems, compositions methods, screens and applications thereof
KR20250012194A (ko) 2013-06-17 2025-01-23 더 브로드 인스티튜트, 인코퍼레이티드 바이러스 구성성분을 사용하여 장애 및 질환을 표적화하기 위한 crispr-cas 시스템 및 조성물의 전달, 용도 및 치료 적용
EP3011030B1 (en) * 2013-06-17 2023-11-08 The Broad Institute, Inc. Optimized crispr-cas double nickase systems, methods and compositions for sequence manipulation
KR20160019553A (ko) 2013-06-17 2016-02-19 더 브로드 인스티튜트, 인코퍼레이티드 유사분열 후 세포의 질병 및 장애를 표적화하고 모델링하기 위한 시스템, 방법 및 조성물의 전달, 유전자 조작 및 최적화
EP3760719A1 (en) * 2013-11-18 2021-01-06 CRISPR Therapeutics AG Crispr-cas system materials and methods
WO2015089364A1 (en) 2013-12-12 2015-06-18 The Broad Institute Inc. Crystal structure of a crispr-cas system, and uses thereof
EP3080259B1 (en) 2013-12-12 2023-02-01 The Broad Institute, Inc. Engineering of systems, methods and optimized guide compositions with new architectures for sequence manipulation
MX2016007325A (es) 2013-12-12 2017-07-19 Broad Inst Inc Composiciones y metodos de uso de sistemas crispr-cas en desordenes debidos a repeticion de nucleotidos.
BR112016013207A2 (pt) 2013-12-12 2017-09-26 Massachusetts Inst Technology administração, uso e aplicações terapêuticas dos sistemas crispr-cas e composições para o hbv e distúrbios e doenças virais
EP3470089A1 (en) 2013-12-12 2019-04-17 The Broad Institute Inc. Delivery, use and therapeutic applications of the crispr-cas systems and compositions for targeting disorders and diseases using particle delivery components
JP6793547B2 (ja) 2013-12-12 2020-12-02 ザ・ブロード・インスティテュート・インコーポレイテッド 最適化機能CRISPR−Cas系による配列操作のための系、方法および組成物
AU2014361781B2 (en) 2013-12-12 2021-04-01 Massachusetts Institute Of Technology Delivery, use and therapeutic applications of the CRISPR -Cas systems and compositions for genome editing
WO2016014837A1 (en) * 2014-07-25 2016-01-28 Sangamo Biosciences, Inc. Gene editing for hiv gene therapy
EP3889260A1 (en) 2014-12-12 2021-10-06 The Broad Institute, Inc. Protected guide rnas (pgrnas)
WO2016106244A1 (en) 2014-12-24 2016-06-30 The Broad Institute Inc. Crispr having or associated with destabilization domains
US10059940B2 (en) * 2015-01-27 2018-08-28 Minghong Zhong Chemically ligated RNAs for CRISPR/Cas9-lgRNA complexes as antiviral therapeutic agents
TWI813532B (zh) 2015-06-18 2023-09-01 美商博得學院股份有限公司 降低脱靶效應的crispr酶突變
WO2016205759A1 (en) 2015-06-18 2016-12-22 The Broad Institute Inc. Engineering and optimization of systems, methods, enzymes and guide scaffolds of cas9 orthologs and variants for sequence manipulation

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1352960A1 (en) * 2002-04-12 2003-10-15 Viruvation B.V. Antiviral therapy on the basis of RNA interference
WO2007014181A2 (en) * 2005-07-25 2007-02-01 Johns Hopkins University Site-specific modification of the human genome using custom-designed zinc finger nucleases
AU2006272634B2 (en) * 2005-07-26 2013-01-24 Sangamo Therapeutics, Inc. Targeted integration and expression of exogenous nucleic acid sequences
US20080003681A1 (en) * 2006-06-28 2008-01-03 Mahalaxmi Gita Bangera Methods for altering cellular susceptibility to infection
US8563314B2 (en) * 2007-09-27 2013-10-22 Sangamo Biosciences, Inc. Methods and compositions for modulating PD1
AU2009257663B2 (en) * 2008-06-09 2014-06-26 New York Medical College Compositions comprising cardiac stem cells overexpressing specific microRNA and methods of their use in repairing damaged myocardium
US8871905B2 (en) * 2009-03-20 2014-10-28 Sangamo Biosciences, Inc. Modification of CXCR4 using engineered zinc finger proteins
EP2462230B1 (en) * 2009-08-03 2015-07-15 Recombinetics, Inc. Methods and compositions for targeted gene modification
CN102071219B (zh) * 2010-11-05 2014-03-12 冯小荣 改腺载体及其在艾滋病预防和治疗药物中的应用

Similar Documents

Publication Publication Date Title
JP2014530603A5 (https=)
JP2016539627A5 (https=)
JP7440027B2 (ja) 多能性幹細胞から免疫細胞療法用t細胞を誘導する方法
Rauch et al. New vaccine technologies to combat outbreak situations
Deering et al. Nucleic acid vaccines: prospects for non-viral delivery of mRNA vaccines
US12442016B2 (en) Scarless genome editing through two-step homology directed repair
WO2016073955A3 (en) Cells lacking b2m surface expression and methods for allogeneic administration of such cells
Kallen et al. A development that may evolve into a revolution in medicine: mRNA as the basis for novel, nucleotide-based vaccines and drugs
CY1122902T1 (el) Ιοσωματιδια αδενο-συσχετιζομενου ιου με καψιδιο παραλλαγματος και μεθοδοι χρησης εξ αυτων
US12485187B2 (en) Method for improving retroviral transduction and gene editing in hematopoietic stem cells using clyclosporin H and UM171
MX2024006041A (es) Celulas t modificadas y metodos para hacer y usar las mismas.
JP2018525979A5 (https=)
AR092317A1 (es) Vectores virales para el tratamiento de distrofia retiniana
MX2021009554A (es) Produccion de virus en cultivos celulares.
WO2016010155A1 (ja) 抗原特異的t細胞受容体遺伝子を有する多能性幹細胞の製造方法
Maring et al. Myocardial regeneration via progenitor cell‐derived exosomes
Murugesan et al. Current approaches and potential challenges in the delivery of gene editing cargos into hematopoietic stem and progenitor cells
Younan et al. Genetically Modified Hematopoietic Stem Cell Transplantation for HIV-1–infected Patients: Can We Achieve a Cure?
WO2012159120A3 (en) Gene therapy based strategy for treating hiv
ES2536605B1 (es) Método de obtención de megacariocitos y plaquetas
Freitas et al. Advances in engineering myeloid cells for cell therapy applications
Wang et al. Engineering hematopoietic stem cells toward a functional cure of human immunodeficiency virus infection
WO2025052001A1 (en) Methods and compositions for improving immune response
Andersen et al. Gene editing in hematopoietic stem cells by co-delivery of Cas9/sgRNA ribonucleoprotein and templates for homology-directed repair in ‘all-in-one’lentivirus-derived nanoparticles
Stevens et al. A temperature-sensitive and less immunogenic Sendai virus for efficient gene editing