humoral response to viral proteins precluding repeat infection. The adeno-associated viral (AAV) vectors have not been exploited extensively partly due to inability to generate high titer helper ...

BHUBANESWAR: In a significant medical breakthrough, India's first human gene therapy with a lentiviral vector for severe ...

about using lentiviruses to engineer cell therapies and the troubleshooting process he undertook to optimize viral production and infection. More on this topic: Viral Vector Platforms for Gene Therapy ...

In 2022, some 40 million people worldwide were living with the HIV virus, a condition that can be treated but not cured.