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An injectable bone marrow-like scaffold enhances T cell immunity after hematopoietic stem cell transplantation.
Shah, Nisarg J; Mao, Angelo S; Shih, Ting-Yu; Kerr, Matthew D; Sharda, Azeem; Raimondo, Theresa M; Weaver, James C; Vrbanac, Vladimir D; Deruaz, Maud; Tager, Andrew M; Mooney, David J; Scadden, David T.
Afiliação
  • Shah NJ; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Mao AS; Wyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA, USA.
  • Shih TY; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Kerr MD; Harvard Stem Cell Institute, Cambridge, MA, USA.
  • Sharda A; Department of Nanoengineering, University of California, San Diego, La Jolla, CA, USA.
  • Raimondo TM; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Weaver JC; Wyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA, USA.
  • Vrbanac VD; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Deruaz M; Wyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA, USA.
  • Tager AM; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
  • Mooney DJ; Wyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA, USA.
  • Scadden DT; Department of Nanoengineering, University of California, San Diego, La Jolla, CA, USA.
Nat Biotechnol ; 37(3): 293-302, 2019 03.
Article em En | MEDLINE | ID: mdl-30742125
Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative treatment for multiple disorders, but deficiency and dysregulation of T cells limit its utility. Here we report a biomaterial-based scaffold that mimics features of T cell lymphopoiesis in the bone marrow. The bone marrow cryogel (BMC) releases bone morphogenetic protein-2 to recruit stromal cells and presents the Notch ligand Delta-like ligand-4 to facilitate T cell lineage specification of mouse and human hematopoietic progenitor cells. BMCs subcutaneously injected in mice at the time of HSCT enhanced T cell progenitor seeding of the thymus, T cell neogenesis and diversification of the T cell receptor repertoire. Peripheral T cell reconstitution increased ~6-fold in mouse HSCT and ~2-fold in human xenogeneic HSCT. Furthermore, BMCs promoted donor CD4+ regulatory T cell generation and improved survival after allogeneic HSCT. In comparison to adoptive transfer of T cell progenitors, BMCs increased donor chimerism, T cell generation and antigen-specific T cell responses to vaccination. BMCs may provide an off-the-shelf approach for enhancing T cell regeneration and mitigating graft-versus-host disease in HSCT.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Medula Óssea / Linfócitos T Reguladores / Transplante de Células-Tronco Hematopoéticas / Alicerces Teciduais / Doença Enxerto-Hospedeiro Limite: Animals / Humans Idioma: En Revista: Nat Biotechnol Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Medula Óssea / Linfócitos T Reguladores / Transplante de Células-Tronco Hematopoéticas / Alicerces Teciduais / Doença Enxerto-Hospedeiro Limite: Animals / Humans Idioma: En Revista: Nat Biotechnol Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos