Lentiviral vectors (LV) are promising tools for gene and cell therapy. They are presently used in several clinical trials as in vivo or ex vivo gene delivery vectors. However their mass production remains a challenge and might limit their potential therapeutic use. New robust and scalable processes are required for industrial production of these vectors. In this review, we focus on the assessment of current LV production methods and evaluate the most critical limitations with a focus on scalability. The key properties of LV are described and their inherent advantages and disadvantages discussed. A brief overview of the quantification methods generally used to characterize vector production is also provided as well as indications on downstre...
Lentiviral vectors (LVs) are promising vectors for gene therapy. Most often, they are used to delive...
Lentiviral vectors (LV) have played a critical role in gene delivery for ex vivo gene-modified cell ...
Lentiviral vectors (LV) have played a critical role in gene delivery for ex vivo gene-modified cell ...
Lentiviral vectors (LVs) have gained value over recent years as gene carriers in gene therapy. These...
Lentiviral vectors (LVs) have gained value over recent years as gene carriers in gene therapy. These...
Lentiviral vectors (LVs) have gained value over recent years as gene carriers in gene therapy. These...
Background: Lentiviral vectors (LV) offer several advantages over other gene delivery vectors. Their...
Lentiviral vectors (LVs) are becoming an important tool in gene and cell therapy and are being utili...
Lentiviral vectors (LVs) are becoming an important tool in gene and cell therapy and are being utili...
Lentiviral vectors (LVs) are becoming an important tool in gene and cell therapy and are being utili...
Lentiviral vectors (LV) represent a key tool for gene and cell therapy applications. The production ...
Lentiviral vectors (LV) have played a critical role in gene delivery for ex vivo gene-modified cell ...
Lentiviral-mediated gene therapy has been proposed for the treatment of a range of diseases, and due...
Lentiviral-mediated gene therapy has been proposed for the treatment of a range of diseases, and due...
Lentiviral vectors (LVs) are promising vectors for gene therapy. Most often, they are used to delive...
Lentiviral vectors (LVs) are promising vectors for gene therapy. Most often, they are used to delive...
Lentiviral vectors (LV) have played a critical role in gene delivery for ex vivo gene-modified cell ...
Lentiviral vectors (LV) have played a critical role in gene delivery for ex vivo gene-modified cell ...
Lentiviral vectors (LVs) have gained value over recent years as gene carriers in gene therapy. These...
Lentiviral vectors (LVs) have gained value over recent years as gene carriers in gene therapy. These...
Lentiviral vectors (LVs) have gained value over recent years as gene carriers in gene therapy. These...
Background: Lentiviral vectors (LV) offer several advantages over other gene delivery vectors. Their...
Lentiviral vectors (LVs) are becoming an important tool in gene and cell therapy and are being utili...
Lentiviral vectors (LVs) are becoming an important tool in gene and cell therapy and are being utili...
Lentiviral vectors (LVs) are becoming an important tool in gene and cell therapy and are being utili...
Lentiviral vectors (LV) represent a key tool for gene and cell therapy applications. The production ...
Lentiviral vectors (LV) have played a critical role in gene delivery for ex vivo gene-modified cell ...
Lentiviral-mediated gene therapy has been proposed for the treatment of a range of diseases, and due...
Lentiviral-mediated gene therapy has been proposed for the treatment of a range of diseases, and due...
Lentiviral vectors (LVs) are promising vectors for gene therapy. Most often, they are used to delive...
Lentiviral vectors (LVs) are promising vectors for gene therapy. Most often, they are used to delive...
Lentiviral vectors (LV) have played a critical role in gene delivery for ex vivo gene-modified cell ...
Lentiviral vectors (LV) have played a critical role in gene delivery for ex vivo gene-modified cell ...