Immune recovery after autologous or rhG-CSF primed PBSC transplantation

Eur J Haematol. 1996 May;56(5):301-7. doi: 10.1111/j.1600-0609.1996.tb00719.x.

Abstract

We performed a prospective study in 17 consecutive patients following Autologous bone marrow (BM) or rhG-CSF primed peripheral blood item cell (PBSC) transplantation, with the objective of comparing immune recovery between both procedures and to evaluate results in rhG-CSF mobilized peripheral blood stem cell transplantation (PBSCT). Kinetics of immune reconstitution showed differences, with a faster recovery of CD3+ and CD8+ T cells, and a more rapid and sustained recovery of CD8+/-/CD56+ natural killer (NK) cells in the PBCSCT group. Autologous bone marrow transplantation (ABMT) was associated with a improved reconstitution of the CD19+/CD5+/-subpopulation. Moreover, rhG-CSF mobilized PBSCT generated a greater recovery of CD8+/-/CD56+ cells than previous data concerning transplantation with peripheral blood (PB) progenitors collected after myelosuppressive chemotherapy or myelosuppressive therapy plus rhG-CSF. Our results show differences in the rate and pattern of B and T lymphocytes reconstitution after ABMT and PBSCT. Additionally, we state an enhancement of CD56+ cells in patients undergoing PBSCT mobilized solely using rhG-CSF.

Publication types

  • Clinical Trial
  • Comparative Study
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD / analysis
  • Bone Marrow Transplantation / immunology*
  • Breast Neoplasms / immunology
  • Breast Neoplasms / therapy
  • Female
  • Granulocyte Colony-Stimulating Factor / therapeutic use*
  • Hematopoietic Stem Cell Transplantation* / methods
  • Humans
  • Killer Cells, Natural / immunology*
  • Leukemia / immunology
  • Leukemia / therapy
  • Lymphoma / immunology
  • Lymphoma / therapy
  • Middle Aged
  • Ovarian Neoplasms / immunology
  • Ovarian Neoplasms / therapy
  • Prospective Studies
  • Recombinant Proteins / therapeutic use
  • Stem Cells / drug effects
  • T-Lymphocytes / immunology*
  • Transplantation, Autologous / immunology
  • Waldenstrom Macroglobulinemia / immunology
  • Waldenstrom Macroglobulinemia / therapy

Substances

  • Antigens, CD
  • Recombinant Proteins
  • Granulocyte Colony-Stimulating Factor