Prolonged allogeneic and xenogeneic microchimerism in unmatched primates without immunosuppression by intrathymic implantation of CD34+ donor marrow cells

Cell Immunol. 1997 Nov 1;181(2):127-38. doi: 10.1006/cimm.1997.1194.

Abstract

Engraftment of stem cell-enriched donor marrow implanted in the thymus of a foreign host might facilitate acceptance of donor-specific organ or tissue grafts. To test this hypothesis, allogeneic and xenogeneic CD34+ marrow cells from unrelated adult male baboons and humans were injected intrathymically in eight infant female baboons, both with and without standard cyclosporine-based immunosuppression. In allogeneic experiments, male (donor) cells, of both T- and B-cell lineages, were detected by PCR in the peripheral blood of all six recipients and persisted for at least 15 months in 2/4 recipients studied longtutudinally. Donor-derived skin grafts survived twice as long as third party grafts in unimmunosuppressed recipients. In xenogeneic protocols, human male (donor) cells were demonstrable for 7 and 15 months, respectively, in two baboon recipients with evidence that implanted human CD34+ cells had produced lymphoid progeny. Survival of donor-specific skin xenografts was prolonged in one of two recipients. These experiments demonstrate that the intrathymic injection of CD34+ marrow cells can result in long-lasting lymphohematopoietic microchimerism in unrelated primates even without immunosuppression and can alter donor-specific skin graft survival.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, CD34 / analysis
  • Bone Marrow Cells / immunology
  • Bone Marrow Transplantation*
  • Chimera
  • Female
  • Graft Enhancement, Immunologic*
  • Graft Survival
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Immune Tolerance
  • Immunoglobulin G / biosynthesis
  • Immunoglobulin G / immunology
  • Isoantibodies / biosynthesis
  • Isoantibodies / immunology
  • Male
  • Papio
  • Skin Transplantation / immunology
  • Thymus Gland / immunology*
  • Transplantation, Heterologous
  • Transplantation, Heterotopic*
  • Transplantation, Homologous

Substances

  • Antigens, CD34
  • Immunoglobulin G
  • Isoantibodies