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Engaging natural antibody responses for the treatment of inflammatory bowel disease via phosphorylcholine-presenting nanofibres.
Curvino, Elizabeth J; Roe, Emily F; Freire Haddad, Helena; Anderson, Alexa R; Woodruff, Mia E; Votaw, Nicole L; Segura, Tatiana; Hale, Laura P; Collier, Joel H.
Afiliação
  • Curvino EJ; Department of Biomedical Engineering, Duke University, Durham, NC, USA.
  • Roe EF; Department of Biomedical Engineering, Duke University, Durham, NC, USA.
  • Freire Haddad H; Department of Biomedical Engineering, Duke University, Durham, NC, USA.
  • Anderson AR; Department of Biomedical Engineering, Duke University, Durham, NC, USA.
  • Woodruff ME; Department of Biomedical Engineering, Duke University, Durham, NC, USA.
  • Votaw NL; Department of Biomedical Engineering, Duke University, Durham, NC, USA.
  • Segura T; Department of Biomedical Engineering, Duke University, Durham, NC, USA.
  • Hale LP; Department of Pathology, Duke University Medical Center, Durham, NC, USA.
  • Collier JH; Department of Biomedical Engineering, Duke University, Durham, NC, USA. joel.collier@duke.edu.
Nat Biomed Eng ; 2023 Nov 27.
Article em En | MEDLINE | ID: mdl-38012308
ABSTRACT
Inflammatory bowel disease lacks a long-lasting and broadly effective therapy. Here, by taking advantage of the anti-infection and anti-inflammatory properties of natural antibodies against the small-molecule epitope phosphorylcholine (PC), we show in multiple mouse models of colitis that immunization of the animals with self-assembling supramolecular peptide nanofibres bearing PC epitopes induced sustained levels of anti-PC antibodies that were both protective and therapeutic. The strength and type of immune responses elicited by the nanofibres could be controlled through the relative valency of PC epitopes and exogenous T-cell epitopes on the nanofibres and via the addition of the adjuvant CpG. The nanomaterial-assisted induction of the production of therapeutic antibodies may represent a durable therapy for inflammatory bowel disease.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos