Precision Wormlike Nanoadjuvant Governs Potency of Vaccination
Author(s) -
Ziyang Sun,
Dongdong Qiao,
Yi Shi,
Matthias Barz,
Lixin Liu,
Yongming Chen
Publication year - 2021
Publication title -
nano letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/acs.nanolett.1c02274
Subject(s) - cpg oligodeoxynucleotide , tlr9 , vaccination , adjuvant , chemistry , agonist , hepatitis b virus , antigen , endosome , cationic polymerization , potency , biophysics , cpg site , virus , virology , receptor , immunology , biology , in vitro , biochemistry , polymer chemistry , gene expression , dna methylation , gene
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.
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