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Alloreactive Regulatory T Cells Allow the Generation of Mixed Chimerism and Transplant Tolerance.
Ruiz, Paulina; Maldonado, Paula; Hidalgo, Yessia; Sauma, Daniela; Rosemblatt, Mario; Bono, Maria Rosa.
Afiliación
  • Ruiz P; Departmento de Biología, Facultad de Ciencias, Universidad de Chile , Santiago , Chile ; Departamento de Tecnología Médica, Facultad de Medicina, Universidad de Chile , Santiago , Chile.
  • Maldonado P; Departmento de Biología, Facultad de Ciencias, Universidad de Chile , Santiago , Chile.
  • Hidalgo Y; Departmento de Biología, Facultad de Ciencias, Universidad de Chile , Santiago , Chile.
  • Sauma D; Departmento de Biología, Facultad de Ciencias, Universidad de Chile , Santiago , Chile.
  • Rosemblatt M; Departmento de Biología, Facultad de Ciencias, Universidad de Chile , Santiago , Chile ; Fundación Ciencia y Vida , Santiago , Chile ; Facultad de Ciencias Biológicas, Universidad Andres Bello , Santiago , Chile.
  • Bono MR; Departmento de Biología, Facultad de Ciencias, Universidad de Chile , Santiago , Chile.
Front Immunol ; 6: 596, 2015.
Article en En | MEDLINE | ID: mdl-26635810
The induction of donor-specific transplant tolerance is one of the main goals of modern immunology. Establishment of a mixed chimerism state in the transplant recipient has proven to be a suitable strategy for the induction of long-term allograft tolerance; however, current experimental recipient preconditioning protocols have many side effects, and are not feasible for use in future therapies. In order to improve the current mixed chimerism induction protocols, we developed a non-myeloablative bone-marrow transplant (NM-BMT) protocol using retinoic acid (RA)-induced alloantigen-specific Tregs, clinically available immunosuppressive drugs, and lower doses of irradiation. We demonstrate that RA-induced alloantigen-specific Tregs in addition to a NM-BMT protocol generates stable mixed chimerism and induces tolerance to allogeneic secondary skin allografts in mice. Therefore, the establishment of mixed chimerism through the use of donor-specific Tregs rather than non-specific immunosuppression could have a potential use in organ transplantation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Front Immunol Año: 2015 Tipo del documento: Article País de afiliación: Chile

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Front Immunol Año: 2015 Tipo del documento: Article País de afiliación: Chile
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