| Literature DB >> 33476764 |
Alexander Marin1, Ananda Chowdhury1, Sarah M Valencia2, Athina Zacharia2, Reinhard Kirnbauer3, Richard B S Roden4, Ligia A Pinto5, Robert H Shoemaker6, Jason D Marshall2, Alexander K Andrianov7.
Abstract
Poly[di(carboxylatomethylphenoxy)phosphazene] (PCMP), a new member of polyphosphazene immunoadjuvant family, is synthesized. In vitro assessment of a new macromolecule revealed hydrolytic degradation profile and immunostimulatory activity comparable to its clinical stage homologue PCPP; however, PCMP was characterized by a beneficial reduced sensitivity to the ionic environment. In vivo evaluation of PCMP potency was conducted with human papillomavirus (HPV) virus-like particles (VLPs) based RG1-VLPs vaccine. In contrast with previously reported self-assembly of polyphosphazene adjuvants with proteins, which typically results in the formation of complexes with multimeric display of antigens, PCMP surface modified VLPs in a composition dependent pattern, which at a high polymer-to VLPs ratio led to stabilization of antigenic particles. Immunization experiments in mice demonstrated that PCMP adjuvanted RG1-VLPs vaccine induced potent humoral immune responses, in particular, on the level of highly desirable protective cross-neutralizing antibodies, and outperformed PCPP and Alhydrogel adjuvanted formulations.Entities:
Keywords: Immunostimulating compounds; Polyphosphazenes; Self-assembly; Vaccine delivery; Virus-like particles
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Year: 2021 PMID: 33476764 PMCID: PMC8184581 DOI: 10.1016/j.nano.2021.102359
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307