In vivo delivery of synthetic DNA-encoded antibodies induces broad HIV-1-neutralizing activity.

Published online

Journal Article

Interventions to prevent HIV-1 infection and alternative tools in HIV cure therapy remain pressing goals. Recently, numerous broadly neutralizing HIV-1 monoclonal antibodies (bNAbs) have been developed that possess the characteristics necessary for potential prophylactic or therapeutic approaches. However, formulation complexities, especially for multiantibody deliveries, long infusion times, and production issues could limit the use of these bNAbs when deployed, globally affecting their potential application. Here, we describe an approach utilizing synthetic DNA-encoded monoclonal antibodies (dmAbs) for direct in vivo production of prespecified neutralizing activity. We designed 16 different bNAbs as dmAb cassettes and studied their activity in small and large animals. Sera from animals administered dmAbs neutralized multiple HIV-1 isolates with activity similar to that of their parental recombinant mAbs. Delivery of multiple dmAbs to a single animal led to increased neutralization breadth. Two dmAbs, PGDM1400 and PGT121, were advanced into nonhuman primates for study. High peak-circulating levels (between 6 and 34 μg/ml) of these dmAbs were measured, and the sera of all animals displayed broad neutralizing activity. The dmAb approach provides an important local delivery platform for the in vivo generation of HIV-1 bNAbs and for other infectious disease antibodies.

Full Text

Duke Authors

Cited Authors

  • Wise, MC; Xu, Z; Tello-Ruiz, E; Beck, C; Trautz, A; Patel, A; Elliott, ST; Chokkalingam, N; Kim, S; Kerkau, MG; Muthumani, K; Jiang, J; Fisher, PD; Ramos, SJ; Smith, TR; Mendoza, J; Broderick, KE; Montefiori, DC; Ferrari, G; Kulp, DW; Humeau, LM; Weiner, DB

Published Date

  • January 6, 2020

Published In

PubMed ID

  • 31697648

Pubmed Central ID

  • 31697648

Electronic International Standard Serial Number (EISSN)

  • 1558-8238

Digital Object Identifier (DOI)

  • 10.1172/JCI132779

Language

  • eng

Conference Location

  • United States