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Lentivirus
Introduction

Lentivirus is a viral vector derived from the Human Immunodeficiency Virus Type 1 (HIV-1). Its pathogenic genes have been removed and replaced with exogenous target genes. As a member of the Retroviridae family, it is a spherical, enveloped virus with a diameter of approximately 80–120 nm. It contains RNA and proteins, with genetic information stored in the RNA. The viral envelope glycoproteins bind to specific receptors on the cell membrane, allowing the virus to enter susceptible target cells.

Vector Features

1. Broad Host Range

Capable of infecting both dividing and non-dividing cells, including a wide variety of cell types such as liver cells, heart cells, nerve cells, endocrine cells, and stem cells.


2. Stable Expression

Exogenous genes can be efficiently delivered into target cells, enabling long-term and stable gene expression. Unlike transient transfection, gene expression is maintained even as cells divide.


3. High Safety

The lentiviral system uses a self-inactivating, third-generation virus backbone to ensure biosafety. No toxicity has been observed, and it is already applied in CAR-T cell therapy.


4. Low Immunogenicity

Can be directly administered in vivo with minimal immune response, reducing the likelihood of rejection or inflammation.

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Lentivirus
Introduction

Lentivirus is a viral vector derived from the Human Immunodeficiency Virus Type 1 (HIV-1). Its pathogenic genes have been removed and replaced with exogenous target genes. As a member of the Retroviridae family, it is a spherical, enveloped virus with a diameter of approximately 80–120 nm. It contains RNA and proteins, with genetic information stored in the RNA. The viral envelope glycoproteins bind to specific receptors on the cell membrane, allowing the virus to enter susceptible target cells.

Vector Features

1. Broad Host Range

Capable of infecting both dividing and non-dividing cells, including a wide variety of cell types such as liver cells, heart cells, nerve cells, endocrine cells, and stem cells.


2. Stable Expression

Exogenous genes can be efficiently delivered into target cells, enabling long-term and stable gene expression. Unlike transient transfection, gene expression is maintained even as cells divide.


3. High Safety

The lentiviral system uses a self-inactivating, third-generation virus backbone to ensure biosafety. No toxicity has been observed, and it is already applied in CAR-T cell therapy.


4. Low Immunogenicity

Can be directly administered in vivo with minimal immune response, reducing the likelihood of rejection or inflammation.

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