Extrathymic T cell differentiation in vitro from human CD34+ stem cells

J Leukoc Biol. 1998 Dec;64(6):733-9. doi: 10.1002/jlb.64.6.733.

Abstract

Although it is well established that T cells are derived from CD34+ stem cells in vivo, and that T cells can develop in the absence of a functioning thymus, it has not proven possible thus far to generate human T cells in vitro from CD34+ cells in the absence of any thymic influence. We now present a limiting dilution cloning culture system that supports the differentiation of highly purified human CD34+ cells to CD3+ T cells in vitro in the complete absence of any thymic components. The culture system features the use of a serum-free medium supplemented with a cocktail of cytokines including flt-3 ligand, interleukin-3 (IL-3), stem cell factor (SCF), and IL-2. CD4+ T cell clones capable of mitogen-stimulated proliferation and response to IL-2, and expressing a varied TCR-Vbeta repertoire were obtained under these conditions. This culture system therefore supports human T lymphopoiesis in the absence of any thymic influence and may prove useful for the evaluation of extrathymic T cell differentiation in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD34*
  • Antigens, Surface / analysis
  • Cattle
  • Cell Differentiation / immunology
  • Cell Division / immunology
  • Cells, Cultured
  • Clone Cells
  • Cytokines / biosynthesis
  • Cytokines / physiology
  • Fetal Blood / physiology
  • Humans
  • Organ Specificity / immunology
  • Receptors, Antigen, T-Cell, alpha-beta / analysis
  • Stem Cells / cytology*
  • Stem Cells / immunology
  • Stem Cells / metabolism
  • T-Lymphocyte Subsets / cytology*
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism
  • Thymus Gland / cytology

Substances

  • Antigens, CD34
  • Antigens, Surface
  • Cytokines
  • Receptors, Antigen, T-Cell, alpha-beta