Results 31 to 40 of about 1,111,723 (286)
Lentiviral Vectors for Ocular Gene Therapy
This review offers the basics of lentiviral vector technologies, their advantages and pitfalls, and an overview of their use in the field of ophthalmology.
Yvan Arsenijevic +3 more
doaj +1 more source
Efficient delivery of Cre-recombinase to neurons in vivo and stable transduction of neurons using adeno-associated and lentiviral vectors [PDF]
BACKGROUND: Inactivating genes in vivo is an important technique for establishing their function in the adult nervous system. Unfortunately, conventional knockout mice may suffer from several limitations including embryonic or perinatal lethality and the
Hermens, Wim T J M C +37 more
core +1 more source
Protection of stem cell-derived lymphocytes in a primate AIDS gene therapy model after in vivo selection [PDF]
Background: There is currently no effective AIDS vaccine, emphasizing the importance of developing alternative therapies. Recently, a patient was successfully transplanted with allogeneic, naturally resistant CCR5-negative (CCR5 delta 32) cells, setting ...
Trobridge, Grant D. +28 more
core +2 more sources
Minimal impact of ZAP on lentiviral vector production and transduction efficiency
The antiviral protein ZAP binds CpG dinucleotides in viral RNA to inhibit replication. This has likely led to the CpG suppression observed in many RNA viruses, including retroviruses.
Helin Sertkaya +11 more
doaj +1 more source
Construction of LILRA2-overexpressing lentiviral vector and establishment of THP-1-LILRA2 stable transfected cell strain [PDF]
Objective To construct a recombinant lentiviral vector overexpressing leukocyte immunoglobulin-like receptor subfamily A member 2 (LILRA2), establish a stable LILRA2-overexpressing human myeloid leukemia mononuclear cell strain(THP-1), and preliminarily ...
HUANG Gaoxiang, WEI Dongmei, YANG Yao, GUO Xianing, ZHOU Kai, LUAN Jing
doaj +1 more source
Lentiviral vectors have remarkable cell entry and gene delivery properties that make them highly attractive for gene therapy. However, all integration-competent gene delivery systems have come under scrutiny for possible adverse insertional events. Circumventing the risk of insertional mutagenesis, integration-deficient human immunodeficiency virus ...
Qasim, Waseem +2 more
openaire +2 more sources
Dendritic cell–targeted lentiviral vector immunization uses pseudotransduction and DNA-mediated STING and cGAS activation [PDF]
Lentiviral vector preparations stimulate immune responses via the host STING and cGAS pathway and pseudotransduction.
Lili Yang +19 more
core +1 more source
Viruses are naturally endowed with the capacity to transfer genetic material between cells. Following early skepticism, engineered viruses have been used to transfer genetic information into thousands of patients, and genetic therapies are currently ...
Jonas Holst Wolff, Jacob Giehm Mikkelsen
doaj +1 more source
Production of lentiviral vectors
Lentiviral vectors (LV) have seen considerably increase in use as gene therapy vectors for the treatment of acquired and inherited diseases. This review presents the state of the art of the production of these vectors with particular emphasis on their large-scale production for clinical purposes.
Merten, O. W., Hebben, M., Bovolenta, C.
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