Lentiviruses are a subclass of retroviruses which are able to transduce both dividing and non-dividing cells. They have been documented to be capable of transducing stem cells, neurons, and immune cells in vivo, with high efficiency and transgene expression stability, making them a highly compelling option for gene therapy approaches.
1 Lentiviruses pose the same risk of mutagenesis and oncogenesis as retroviruses.
1 In addition, while both retroviruses and lentiviruses can be pathogenic if they become replication-capable, lentiviruses present a greater safety risk because of their ability to induce chronic and fatal diseases, including AIDS.
1 For further expansion on related topics please visit our viral vector section in the resource center
here.
References:
1. J.B. Connolly, “Lentiviruses in gene therapy clinical research,”
Gene Ther 9(24): 1730-1734, 2002.