High-affinity antigen association to cationic liposomes via coiled coil-forming peptides induces a strong antigen-specific CD4+ T-cell response
نویسندگان
چکیده
Liposomes are widely investigated as vaccine delivery systems, but antigen loading efficiency can be low. Moreover, adsorbed may rapidly desorb under physiological conditions. Encapsulation of antigens overcomes the latter problem results in significant loss during preparation and purification liposomes. Here, we propose an alternative attachment method, based on a complementary heterodimeric coiled coil peptide pair pepK pepE. PepK was conjugated to cholesterol (yielding CPK) pepE covalently linked model OVA323 pepE-OVA323). CPK incorporated lipid bilayer cationic liposomes (180 nm size). Antigen associated more efficiently functionalized (Kd 166 nM) than not detectable). In vivo co-localization strongly increased upon CPK-functionalization (35% -> 80%). CPK-functionalized induced 5-fold stronger CD4+ T-cell proliferation non-functionalized vitro. Both formulations were able induce strong expansion mice, IFN-y IL-10 production observed after immunization with conclusion, association via liposomes, vitro response vivo.
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ژورنال
عنوان ژورنال: European Journal of Pharmaceutics and Biopharmaceutics
سال: 2021
ISSN: ['0939-6411', '1873-3441']
DOI: https://doi.org/10.1016/j.ejpb.2020.11.005