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Biomaterial vaccines capturing pathogen-associated molecular patterns protect against bacterial infections and septic shock.
Super, Michael; Doherty, Edward J; Cartwright, Mark J; Seiler, Benjamin T; Langellotto, Fernanda; Dimitrakakis, Nikolaos; White, Des A; Stafford, Alexander G; Karkada, Mohan; Graveline, Amanda R; Horgan, Caitlin L; Lightbown, Kayla R; Urena, Frank R; Yeager, Chyenne D; Rifai, Sami A; Dellacherie, Maxence O; Li, Aileen W; Leese-Thompson, Collin; Ijaz, Hamza; Jiang, Amanda R; Chandrasekhar, Vasanth; Scott, Justin M; Lightbown, Shanda L; Ingber, Donald E; Mooney, David J.
Afiliação
  • Super M; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Doherty EJ; Vascular Biology Program and Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.
  • Cartwright MJ; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Seiler BT; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Langellotto F; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Dimitrakakis N; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • White DA; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Stafford AG; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Karkada M; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Graveline AR; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Horgan CL; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Lightbown KR; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Urena FR; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Yeager CD; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Rifai SA; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Dellacherie MO; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Li AW; Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Leese-Thompson C; Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Ijaz H; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Jiang AR; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Chandrasekhar V; Vascular Biology Program and Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.
  • Scott JM; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Lightbown SL; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Ingber DE; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • Mooney DJ; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
Nat Biomed Eng ; 6(1): 8-18, 2022 01.
Article em En | MEDLINE | ID: mdl-34239117
ABSTRACT
Most bacterial vaccines work for a subset of bacterial strains or require the modification of the antigen or isolation of the pathogen before vaccine development. Here we report injectable biomaterial vaccines that trigger potent humoral and T-cell responses to bacterial antigens by recruiting, reprogramming and releasing dendritic cells. The vaccines are assembled from regulatorily approved products and consist of a scaffold with absorbed granulocyte-macrophage colony-stimulating factor and CpG-rich oligonucleotides incorporating superparamagnetic microbeads coated with the broad-spectrum opsonin Fc-mannose-binding lectin for the magnetic capture of pathogen-associated molecular patterns from inactivated bacterial-cell-wall lysates. The vaccines protect mice against skin infection with methicillin-resistant Staphylococcus aureus, mice and pigs against septic shock from a lethal Escherichia coli challenge and, when loaded with pathogen-associated molecular patterns isolated from infected animals, uninfected animals against a challenge with different E. coli serotypes. The strong immunogenicity and low incidence of adverse events, a modular manufacturing process, and the use of components compatible with current good manufacturing practice could make this vaccine technology suitable for responding to bacterial pandemics and biothreats.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Choque Séptico / Infecções Bacterianas / Vacinas / Staphylococcus aureus Resistente à Meticilina Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Choque Séptico / Infecções Bacterianas / Vacinas / Staphylococcus aureus Resistente à Meticilina Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article