B lymphocyte regeneration in marrow and blood after autologous bone marrow transplantation: increased numbers of B cells carrying activation and progression markers

Leuk Res. 1989;13(9):791-7. doi: 10.1016/0145-2126(89)90092-1.

Abstract

The reconstitution of B cells in the bone marrow and peripheral blood was prospectively studied in 27 patients undergoing autologous bone marrow transplantation (ABMT). No major differences in B cell regeneration patterns were recorded between patients receiving marrows purged of B cells (anti-CD10 + 19; n = 17) and patients receiving unpurged marrows (n = 10). Compared with healthy controls, elevated absolute and relative numbers of B cells were recorded in the blood and marrow at +6 and +12 months in both groups of patients. CD23+ B cells were severely depressed during the first three months post ABMT, indicating immaturity. A twofold increase in B cells carrying the activation marker 4F2 was recorded in the marrow at +1 month. Serum immunoglobulin levels (IgG, IgA, IgM) were within low-normal range throughout the study. The depressed B cell responses reported after allogeneic and autologous BMT could in part be explained by the low expression of the CD23 antigen on B cells after such therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD19
  • Antigens, Differentiation, B-Lymphocyte
  • Antigens, Surface / analysis
  • B-Lymphocytes / cytology*
  • Bone Marrow Transplantation / pathology*
  • Cell Division
  • Flow Cytometry
  • Humans
  • Immunoglobulins / analysis
  • Lymphocyte Activation
  • Prospective Studies
  • Receptors, Fc / analysis
  • Receptors, IgE
  • Transplantation, Autologous

Substances

  • Antigens, CD19
  • Antigens, Differentiation, B-Lymphocyte
  • Antigens, Surface
  • Immunoglobulins
  • Receptors, Fc
  • Receptors, IgE