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Identification of a humanized mouse model for functional testing of immune-mediated biomaterial foreign body response.
Doloff, Joshua C; Ma, Minglin; Sadraei, Atieh; Tam, Hok Hei; Farah, Shady; Hollister-Lock, Jennifer; Vegas, Arturo J; Veiseh, Omid; Quiroz, Victor M; Rakoski, Amanda; Aresta-DaSilva, Stephanie; Bader, Andrew R; Griffin, Marissa; Weir, Gordon C; Brehm, Michael A; Shultz, Leonard D; Langer, Robert; Greiner, Dale L; Anderson, Daniel G.
Affiliation
  • Doloff JC; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 500 Main St., Cambridge, MA 02139, USA.
  • Ma M; Department of Anesthesiology, Boston Children's Hospital, 300 Longwood Ave., Boston, MA 02115, USA.
  • Sadraei A; Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, MA 02139, USA.
  • Tam HH; Department of Biomedical Engineering, Translational Tissue Engineering Center, Johns Hopkins University, Baltimore, MD 21287, USA.
  • Farah S; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 500 Main St., Cambridge, MA 02139, USA.
  • Hollister-Lock J; Department of Anesthesiology, Boston Children's Hospital, 300 Longwood Ave., Boston, MA 02115, USA.
  • Vegas AJ; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 500 Main St., Cambridge, MA 02139, USA.
  • Veiseh O; Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, MA 02139, USA.
  • Quiroz VM; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 500 Main St., Cambridge, MA 02139, USA.
  • Rakoski A; Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, MA 02139, USA.
  • Aresta-DaSilva S; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 500 Main St., Cambridge, MA 02139, USA.
  • Bader AR; Department of Anesthesiology, Boston Children's Hospital, 300 Longwood Ave., Boston, MA 02115, USA.
  • Griffin M; Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, MA 02139, USA.
  • Weir GC; Section on Islet Cell and Regenerative Biology, Research Division, Joslin Diabetes Center, One Joslin Place, Boston, MA 02215, USA.
  • Brehm MA; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 500 Main St., Cambridge, MA 02139, USA.
  • Shultz LD; Department of Anesthesiology, Boston Children's Hospital, 300 Longwood Ave., Boston, MA 02115, USA.
  • Langer R; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 500 Main St., Cambridge, MA 02139, USA.
  • Greiner DL; Department of Anesthesiology, Boston Children's Hospital, 300 Longwood Ave., Boston, MA 02115, USA.
  • Anderson DG; Department of Biomedical Engineering, Translational Tissue Engineering Center, Johns Hopkins University, Baltimore, MD 21287, USA.
Sci Adv ; 9(24): eade9488, 2023 06 16.
Article in En | MEDLINE | ID: mdl-37327334
ABSTRACT
Biomedical devices comprise a major component of modern medicine, however immune-mediated fibrosis and rejection can limit their function over time. Here, we describe a humanized mouse model that recapitulates fibrosis following biomaterial implantation. Cellular and cytokine responses to multiple biomaterials were evaluated across different implant sites. Human innate immune macrophages were verified as essential to biomaterial rejection in this model and were capable of cross-talk with mouse fibroblasts for collagen matrix deposition. Cytokine and cytokine receptor array analysis confirmed core signaling in the fibrotic cascade. Foreign body giant cell formation, often unobserved in mice, was also prominent. Last, high-resolution microscopy coupled with multiplexed antibody capture digital profiling analysis supplied spatial resolution of rejection responses. This model enables the study of human immune cell-mediated fibrosis and interactions with implanted biomaterials and devices.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biocompatible Materials / Foreign Bodies Type of study: Diagnostic_studies / Etiology_studies Limits: Animals / Humans Language: En Journal: Sci Adv Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biocompatible Materials / Foreign Bodies Type of study: Diagnostic_studies / Etiology_studies Limits: Animals / Humans Language: En Journal: Sci Adv Year: 2023 Document type: Article