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Next generation polyphosphazene immunoadjuvant: Synthesis, self-assembly and in vivo potency with human papillomavirus VLPs-based vaccine.
Marin, Alexander; Chowdhury, Ananda; Valencia, Sarah M; Zacharia, Athina; Kirnbauer, Reinhard; Roden, Richard B S; Pinto, Ligia A; Shoemaker, Robert H; Marshall, Jason D; Andrianov, Alexander K.
Afiliación
  • Marin A; Institute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD, United States.
  • Chowdhury A; Institute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD, United States.
  • Valencia SM; Cancer ImmunoPrevention Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD, United States.
  • Zacharia A; Cancer ImmunoPrevention Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD, United States.
  • Kirnbauer R; Department of Dermatology, Medical University of Vienna, Vienna, Austria.
  • Roden RBS; Department of Pathology, Johns Hopkins University, Baltimore, MD, , United States.
  • Pinto LA; HPV Immunology laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD, United States.
  • Shoemaker RH; Chemopreventive Agent Development Research Group, Division of Cancer Prevention, National Cancer Institute, Rockville, MD, United States.
  • Marshall JD; Cancer ImmunoPrevention Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD, United States.
  • Andrianov AK; Institute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD, United States. Electronic address: aandrianov@umd.edu.
Nanomedicine ; 33: 102359, 2021 04.
Article en En | MEDLINE | ID: mdl-33476764
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Compuestos Organofosforados / Polímeros / Materiales Biocompatibles / Adyuvantes Inmunológicos / Infecciones por Papillomavirus / Vacunas contra Papillomavirus / Vacunas de Partículas Similares a Virus Límite: Animals / Female / Humans Idioma: En Revista: Nanomedicine Asunto de la revista: BIOTECNOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Compuestos Organofosforados / Polímeros / Materiales Biocompatibles / Adyuvantes Inmunológicos / Infecciones por Papillomavirus / Vacunas contra Papillomavirus / Vacunas de Partículas Similares a Virus Límite: Animals / Female / Humans Idioma: En Revista: Nanomedicine Asunto de la revista: BIOTECNOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos