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RESEARCH PRODUCT

Precision wormlike nanoadjuvant governs potency of vaccination

Dongdong QiaoLixin LiuYi ShiMatthias BarzMatthias BarzYongming ChenZiyang Sun

subject

Hepatitis B virusCpG OligodeoxynucleotideChemistryMechanical Engineeringmedicine.medical_treatmentVaccinationTLR9BioengineeringGeneral ChemistryCondensed Matter Physicsmedicine.disease_causeMolecular biologyDisease Models AnimalMiceImmune systemCpG siteAdjuvants ImmunologicmedicineAnimalsGeneral Materials ScienceReceptorAdjuvantLate endosome

description

It remains unclear how the precise length of one-dimensional nanovehicles influences the characters of vaccination. Here, a unimolecular nanovehicle with tailored size and aspect ratio (AR) is applied to deliver CpG oligodeoxynucleotide, a Toll-like receptor (TLR) 9 agonist, as an adjuvant of recombinant hepatitis B virus surface antigen (rHBsAg), for treating chronic hepatitis B (CHB). Cationic nanovehicles with fixed width (ca. 45 nm) but varied length (46 nm-180 nm), AR from 1 to 4, are prepared through controlled polymerization and are loaded with CpG by electrostatic interaction. We reveal that the nanoadjuvant with AR = 2 shows the highest retention in proximal lymph nodes. Importantly, it is more easily internalized into antigen-presenting cells and accumulates in the late endosome, where TLR9 is located. Such a nanoadjuvant exhibits the strongest immune response with rHBsAg to clear the hepatitis B virus in the CHB mouse model, showing that the AR of nanovehicles governs the efficiency of vaccination.

10.1021/acs.nanolett.1c02274https://doi.org/10.1021/acs.nanolett.1c02274