4.3 Article

Keratinocyte growth factor enhanced immune reconstitution in murine allogeneic umbilical cord blood cell transplant

Journal

LEUKEMIA & LYMPHOMA
Volume 52, Issue 8, Pages 1556-1566

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.3109/10428194.2011.573037

Keywords

Umbilical cord blood transplant; keratinocyte growth factor; immune reconstitution; graft-versus-leukemia; murine model

Funding

  1. Suzhou Science and Development Program [SS0718, KF200943, H200721]
  2. Ministry of Education of the People's Republic of China [20093201110010]
  3. Scientific Research Foundation of the Health Ministry of China [LJ200626]
  4. National Science and Technology Major Program [2009ZX09503]
  5. Suzhou University [Q312203210]

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Umbilical cord blood (UCB) is used increasingly as a source of hematopoietic cells because of a lower risk of graft-versus-host disease (GVHD). Myeloablative conditioning before allogeneic umbilical cord blood transplant (allo-UCBT) results in thymic epithelial cell injury and T-cell immune deficiency. Full-term fetal blood cells were used as hematopoietic cells in a previous murine allo-UCBT model with a limited number of mice surviving the myeloablative conditioning. We designed a viable murine allo-UCBT protocol with platelet concentrate support. Keratinocyte growth factor (KGF) is a mitogen of thymic epithelial cells that promotes recovery of thymic epithelium when given before total body irradiation (TBI)-containing conditioning in experimental murine models. We hypothesized that KGF pre-administration would improve post-allo-UCBT thymopoiesis. To test this hypothesis, allo-UCBT recipient mice were given KGF or control saline prior to UCBT. Platelet concentrate support significantly improved the survival rate of murine allo-UCBT recipients. KGF administration significantly increased donor-derived T and natural killer T (NKT) cells at day +35 in spleens of allo-UCBT recipients. KGF administration also improved thymic function after allo-UCBT, resulting in higher copies of signal joint T-cell receptor rearrangement excision circles (sjTRECs) in splenocytes. Finally, we found that KGF pre-administration could enhance the graft-versus-leukemia effect. In conclusion, KGF can be administered safely to recipients of allo-UCBT to enhance T-cell immune reconstitution.

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