Inhibitory oligonucleotides specifically block effects of stimulatory CpG oligonucleotides in B cells

Eur J Immunol. 2002 May;32(5):1212-22. doi: 10.1002/1521-4141(200205)32:5<1212::AID-IMMU1212>3.0.CO;2-D.


Reaction to certain motifs in bacterial DNA is an important function of natural immunity. For example, single stranded oligonucleotides (ODN) containing the motif "not C, unmethylated C, G, not G" are powerful mitogens and apoptosis inhibitors for mouse spleen B cells. But replacing GCGTT or ACGTT with GCGGG or ACGGG converted a stimulatory 15-mer ODN into an inhibitory ODN. All inhibitory ODN had three consecutive G, and a fourth G increased inhibitory activity, but a deazaguanosine substitution to prevent planar stacking did not affect activity. Inhibitory ODN blocked apoptosis protection and cell-cycle entry induced by stimulatory ODN, but not that induced by lipopolysaccharide, anti-CD40 or anti-IgM+IL-4. ODN-driven up-regulation of cyclin D(2), c-Myc, c-Fos, c-Jun and Bcl(XL) and down-regulation of cyclin kinase inhibitor p27(kip1) were all blocked by inhibitory ODN. The relative potency of a series of stimulatory and inhibitory ODN was the same for all readouts measured. Interference with uptake of stimulatory ODN could not account for their inhibitory effects. Even if addition of inhibitory ODN was delayed several hours, partial inhibition of stimulatory ODN effects occurred. Inhibitory ODN hold potential as antidotes for excessive ODN stimulation in the clinical setting and provide an important tool for studying ODN recognition.

Publication types

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

MeSH terms

  • Adjuvants, Immunologic / chemistry
  • Adjuvants, Immunologic / pharmacology
  • Animals
  • Apoptosis / drug effects
  • B-Lymphocytes / cytology
  • B-Lymphocytes / drug effects*
  • B-Lymphocytes / immunology*
  • Base Sequence
  • Biological Transport, Active
  • Cell Cycle / drug effects
  • Cell Membrane / metabolism
  • CpG Islands
  • Female
  • Immunosuppressive Agents / chemistry
  • Immunosuppressive Agents / pharmacology
  • In Vitro Techniques
  • Mice
  • Oligodeoxyribonucleotides / genetics
  • Oligodeoxyribonucleotides / immunology
  • Oligodeoxyribonucleotides / pharmacokinetics
  • Oligodeoxyribonucleotides / pharmacology*
  • Signal Transduction
  • Thionucleotides / genetics
  • Thionucleotides / immunology
  • Thionucleotides / pharmacology


  • Adjuvants, Immunologic
  • Immunosuppressive Agents
  • Oligodeoxyribonucleotides
  • Thionucleotides