DNA damage and repair in epithelium after allogeneic hematopoietic stem cell transplantation

Int J Mol Sci. 2012 Nov 27;13(12):15813-25. doi: 10.3390/ijms131215813.

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) in humans, following hematoablative treatment, results in biological chimeras. In this case, the transplanted hematopoietic, immune cells and their derivatives can be considered the donor genotype, while the other tissues are the recipient genotype. The first sequel, which has been recognized in the development of chimerical organisms after allo-HSCT, is the graft versus host (GvH) reaction, in which the new developed immune cells from the graft recognize the host's epithelial cells as foreign and mount an inflammatory response to kill them. There is now accumulating evidence that this chronic inflammatory tissue stress may contribute to clinical consequences in the transplant recipient. It has been recently reported that host epithelial tissue acquire genomic alterations and display a mutator phenotype that may be linked to the occurrence of a GvH reaction. The current review discusses existing data on this recently discovered phenomenon and focuses on the possible pathogenesis, clinical significance and therapeutic implications.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Allografts
  • Animals
  • DNA Damage*
  • DNA Repair*
  • Epithelial Cells / metabolism*
  • Epithelial Cells / pathology
  • Epithelium / metabolism
  • Epithelium / pathology
  • Graft vs Host Disease / metabolism*
  • Graft vs Host Disease / pathology
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Inflammation / metabolism
  • Inflammation / pathology