Activating CTL precursors to reveal CTL function without skewing the repertoire by in vitro expansion

Eur J Immunol. 2001 Dec;31(12):3557-66. doi: 10.1002/1521-4141(200112)31:12<3557::aid-immu3557>3.0.co;2-o.

Abstract

Detection of the functional CD8(+) CTL response usually requires in vitro restimulation. The differences between the CD8(+) CTL repertoire in freshly isolated precursor cells and CD8(+) CTL after short-term in vitro expansion have been generally assumed to be minimal, but have never been defined experimentally. Using staining with P18-I10/H-2D(d) tetramers and monoclonal antibodies (mAb) against Vbeta, we show the surprising result that there was significant skewing of the CD8(+) CTL repertoire after just 7 days of stimulation. In contrast, we found that overnight incubation of precursor cells with peptide allows the functional assessment of CD8(+) CTL (which cannot be detected ex vivo from freshly isolated cells) without changing the absolute number of antigen-specific CTL as measured by tetramer staining or the repertoire of TCR analyzed with mAb. This study affords a better understanding of the differences between the ex vivo and in vitro stimulated CTL repertoire, and provides an approach to reveal a more faithful representation of the functional in vivo CTL response without skewing of the repertoire of T cells detected.

MeSH terms

  • Animals
  • Female
  • HIV Envelope Protein gp160 / immunology
  • HIV-1 / immunology
  • Hematopoietic Stem Cells / immunology*
  • Lymphocyte Activation*
  • Mice
  • Mice, Inbred BALB C
  • Receptors, Antigen, T-Cell, alpha-beta / analysis
  • T-Lymphocytes, Cytotoxic / immunology*

Substances

  • HIV Envelope Protein gp160
  • Receptors, Antigen, T-Cell, alpha-beta