4.7 Article

mRNA Delivery System for Targeting Antigen-Presenting Cells In Vivo

期刊

ADVANCED HEALTHCARE MATERIALS
卷 7, 期 17, 页码 -

出版社

WILEY
DOI: 10.1002/adhm.201800335

关键词

antigen-presenting cells transfection; immunotherapy; mRNA encapsulation and delivery; oligopeptide-modified poly-(beta-aminoester) polyplexes; spleen

资金

  1. MINECO/FEDER [RTC-2015-3751-1, SAF2015-64927-C2-1-R, SAF2015-64927-C2-2-R]
  2. Instituto de Salud Carlos III (Red Tematica de Investigacion Cooperativa en Terapia Celular-TERCEL)
  3. VI National R&DI Plan2008-2011
  4. Iniciativa Ingenio 2010
  5. Consolider Program
  6. CIBER Actions
  7. Instituto de Salud Carlos III
  8. European Regional Development Fund
  9. MINECO
  10. Agencia de Gestio d'Ajuts Universitaris i de Recerca (AGAUR) from Generalitat de Catalunya [SGR 2014 1170]

向作者/读者索取更多资源

The encapsulation of mRNA in nanosystems as gene vaccines for immunotherapy purposes has experienced an exponential increase in recent years. Despite the many advantages envisaged within these approaches, their application in clinical treatments is still limited due to safety issues. These issues can be attributed, in part, to liver accumulation of most of the designed nanosystems and to the inability to transfect immune cells after an intravenous administration. In this context, this study takes advantage of the known versatile properties of the oligopeptide end-modified poly (beta-amino esters) (OM-PBAEs) to complex mRNA and form discrete nanoparticles. Importantly, it is demonstrated that the selection of the appropriate end-oligopeptide modifications enables the specific targeting and major transfection of antigen-presenting cells (APC) in vivo, after intravenous administration, thus enabling their use for immunotherapy strategies. Therefore, with this study, it can be confirmed that OM-PBAE are appropriate systems for the design of mRNA-based immunotherapy approaches aimed to in vivo transfect APCs and trigger immune responses to fight either tumors or infectious diseases.

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