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 (enExample) 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 (enExample)
EP (1) EP2764102A4 (enExample)
JP (1) JP2014530603A (enExample)
AU (1) AU2012318562A1 (enExample)
CA (1) CA2849920A1 (enExample)
HK (1) HK1200491A1 (enExample)
WO (1) WO2013052681A1 (enExample)

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
WO2014093701A1 (en) 2012-12-12 2014-06-19 The Broad Institute, Inc. Functional genomics using crispr-cas systems, compositions, methods, knock out libraries and applications thereof
AU2013359199C1 (en) 2012-12-12 2021-06-17 Massachusetts Institute Of Technology Delivery, engineering and optimization of systems, methods and compositions for sequence manipulation and therapeutic applications
ES2701749T3 (es) 2012-12-12 2019-02-25 Broad Inst Inc Métodos, modelos, sistemas y aparatos para identificar secuencias diana para enzimas Cas o sistemas CRISPR-Cas para secuencias diana y transmitir resultados de los mismos
SG11201510284XA (en) 2013-06-17 2016-01-28 Broad Inst Inc Delivery and use of the crispr-cas systems, vectors and compositions for hepatic targeting and therapy
AU2014281026B2 (en) 2013-06-17 2020-05-28 Massachusetts Institute Of Technology Delivery, engineering and optimization of tandem guide systems, methods and compositions for sequence manipulation
WO2014204725A1 (en) * 2013-06-17 2014-12-24 The Broad Institute Inc. Optimized crispr-cas double nickase systems, methods and compositions for sequence manipulation
RU2716421C2 (ru) 2013-06-17 2020-03-11 Те Брод Инститьют Инк. Доставка, применение и применения в терапии систем crispr-cas и композиций для целенаправленного воздействия на нарушения и заболевания с использованием вирусных компонентов
CA2915845A1 (en) 2013-06-17 2014-12-24 The Broad Institute, Inc. Delivery, engineering and optimization of systems, methods and compositions for targeting and modeling diseases and disorders of post mitotic cells
EP3725885A1 (en) 2013-06-17 2020-10-21 The Broad Institute, Inc. Functional genomics using crispr-cas systems, compositions methods, screens and applications thereof
EP3071695A2 (en) * 2013-11-18 2016-09-28 Crispr Therapeutics AG Crispr-cas system materials and methods
KR20250068794A (ko) 2013-12-12 2025-05-16 더 브로드 인스티튜트, 인코퍼레이티드 게놈 편집을 위한 crispr-cas 시스템 및 조성물의 전달, 용도 및 치료적 응용
EP3080261B1 (en) 2013-12-12 2019-05-22 The Broad Institute, Inc. Delivery, use and therapeutic applications of the crispr-cas systems and compositions for hbv and viral diseases and disorders
WO2015089364A1 (en) 2013-12-12 2015-06-18 The Broad Institute Inc. Crystal structure of a crispr-cas system, and uses thereof
AU2014362245A1 (en) 2013-12-12 2016-06-16 Massachusetts Institute Of Technology Compositions and methods of use of CRISPR-Cas systems in nucleotide repeat disorders
WO2015089486A2 (en) 2013-12-12 2015-06-18 The Broad Institute Inc. Systems, methods and compositions for sequence manipulation with optimized functional crispr-cas systems
EP4219699A1 (en) 2013-12-12 2023-08-02 The Broad Institute, Inc. Engineering of systems, methods and optimized guide compositions with new architectures for sequence manipulation
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
US9757420B2 (en) 2014-07-25 2017-09-12 Sangamo Therapeutics, Inc. Gene editing for HIV gene therapy
EP3985115A1 (en) 2014-12-12 2022-04-20 The Broad Institute, Inc. Protected guide rnas (pgrnas)
CA2970370A1 (en) 2014-12-24 2016-06-30 Massachusetts Institute Of Technology 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
MX392008B (es) 2015-06-18 2025-03-21 Broad Inst Inc Mutaciones de la enzima crispr que reducen los efectos fuera del blanco
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
SG10201508995QA (en) * 2005-07-26 2015-11-27 Sangamo Biosciences 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
US8193161B2 (en) * 2008-06-09 2012-06-05 New York Medical College Compositions comprising cardiac stem cells overexpressing specific micrornas and methods of their use in repairing damaged myocardium
EP2408921B1 (en) * 2009-03-20 2017-04-19 Sangamo BioSciences, Inc. Modification of cxcr4 using engineered zinc finger proteins
DK2462230T3 (en) * 2009-08-03 2015-10-19 Recombinetics Inc METHODS AND COMPOSITIONS FOR TARGETED RE-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 (enExample)
Qu et al. Circular RNA vaccines against SARS-CoV-2 and emerging variants
JP2016539627A5 (enExample)
Rauch et al. New vaccine technologies to combat outbreak situations
Deering et al. Nucleic acid vaccines: prospects for non-viral delivery of mRNA vaccines
WO2016073955A3 (en) Cells lacking b2m surface expression and methods for allogeneic administration of such cells
US20230348932A1 (en) Scarless genome editing through two-step homology directed repair
Kallen et al. A development that may evolve into a revolution in medicine: mRNA as the basis for novel, nucleotide-based vaccines and drugs
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.
MX349138B (es) Variones de virus adeno-asociados con capside variante y sus metodos de uso.
AR092317A1 (es) Vectores virales para el tratamiento de distrofia retiniana
Sioud et al. Silencing of indoleamine 2, 3-dioxygenase enhances dendritic cell immunogenicity and antitumour immunity in cancer patients
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
JP2024519524A (ja) 疾患の処置のために有用なレンチウイルスベクター
Koenecke et al. MicroRNA in T-cell development and T-cell mediated acute graft-versus-host disease
Younan et al. Genetically Modified Hematopoietic Stem Cell Transplantation for HIV-1–infected Patients: Can We Achieve a Cure?
Murugesan et al. Current approaches and potential challenges in the delivery of gene editing cargos into hematopoietic stem and progenitor cells
JP2014515258A5 (enExample)
Yao et al. Mesenchymal stem cells as novel micro‐ribonucleic acid delivery vehicles in kidney disease
ES2536605B1 (es) Método de obtención de megacariocitos y plaquetas
Wang et al. Engineering hematopoietic stem cells toward a functional cure of human immunodeficiency virus infection
Stevens et al. A temperature-sensitive and less immunogenic Sendai virus for efficient gene editing