| Literature DB >> 29573820 |
Lutz Nuhn1, Lien Van Hoecke2, Kim Deswarte3, Bert Schepens2, Yupeng Li4, Bart N Lambrecht3, Stefaan De Koker2, Sunil A David4, Xavier Saelens2, Bruno G De Geest5.
Abstract
Improving the immunogenicity of subunit vaccines, in particular skewing of the immune response towards Th1 type immunity, is crucial for the development of effective vaccines against intracellular infections and for the development of anti-cancer vaccines. Small molecule TLR7/8 agonist hold high potential for this purpose, but suffer from an undesirable pharmacokinetic profile, resulting in systemic inflammatory responses. An effective solution to this problem is covalent ligation to a larger carrier. Here, a degradable nanogel carrier containing a covalently linked imidazoquinoline (IMDQ) TLR7/8 agonist is explored as adjuvant for vaccination against the respiratory syncytial virus (RSV). In vitro and in vivo experiments in mice provide a solid rational base for preferring nanogels over soluble polymers as IMDQ carrier in terms of cellular uptake and lymph node accumulation.Entities:
Keywords: Lymph nodes; Nanogels; RSV; TLR agonist; Vaccine
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Year: 2018 PMID: 29573820 DOI: 10.1016/j.biomaterials.2018.03.026
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479