A New Approach to mRNA Delivery
Lentivirus, adenovirus, adeno-associated virus (AAV), and lipid nanoparticle (LNP)Â are currently the main delivery vectors used for human gene therapy, but some of these delivery vectors can randomly integrate into the genome, some are ineffective, and some can trigger unintended immune responses. The entire biomedical community is striving to develop new and more powerful molecular therapies,…