Elsevier

Cellular Immunology

Volume 203, Issue 1, 10 July 2000, Pages 55-65
Cellular Immunology

Regular Article
The Immune Response Modifiers Imiquimod and R-848 Are Potent Activators of B Lymphocytes

https://doi.org/10.1006/cimm.2000.1673Get rights and content

Abstract

Imiquimod and R-848 are members of a family of immune response modifiers that stimulate cytokine production in monocyte/macrophages and dendritic cell cultures. This study evaluated the effects of the imidazoquinolines, imiquimod and R-848, on B lymphocyte activation. Both agents induced proliferation of murine T-cell-depleted and highly purified splenic B cell preparations as well as purified human B cells. Resting and activated B cells responded to these agents, with activated cells responding more efficiently. B cells from the LPS-hyporesponsive C3H/HeJ mice and guanosine-hyporesponsive SJL mice proliferated in response to imiquimod and R-848, indicating a different mechanism of action than lipopolysaccharide and guanine nucleosides. B cells were also stimulated by imiquimod and R-848 to produce increased immunoglobulin levels. Increased expression of a number of B cell activation markers were seen following imiquimod or R-848 stimulation. Finally, R-848 was shown to act as a vaccine adjuvant enhancing OVA-specific IgG2a levels while suppressing total IgE. These results indicate that R-848 and imiquimod are potent activators of B lymphocytes and are capable of augmenting antigen-specific immunoglobulin production.

References (37)

  • Z.K. Ballas et al.

    Induction of NK activity in murine and human cells by CpG motifs in oligodeoxynucleotides and bacterial DNA

    J. Immunol.

    (1996)
  • S. Yamamoto et al.

    DNA from bacteria, but not vertebrates, induces interferons, activates natural killer cells and inhibits tumor growth

    Microbiol. Immunol.

    (1992)
  • A.G. Johnson

    Modulation of the immune system by synthetic polynucleotides

    Springer Semin. Immunopathol.

    (1979)
  • J.Y. Djeu et al.

    Role of macrophages in the augmentation of mouse natural killer cell activity by Poly I:C and interferon

    J. Immunol.

    (1979)
  • B.L. Pope et al.

    Enhancement of immunostimulatory activity by dual substitution of C8-substituted guanine ribonucleosides: Correlation with increased cytokine secretion

    J. Immunother. Emphasis Tumor Immunol.

    (1995)
  • C.J. Harrison et al.

    Modification of immunological responses and clinical disease during topical R-837 treatment of genital HSV-2 infection

    Antiviral Res.

    (1988)
  • M. Chen et al.

    Efficacy of S-26308 against guinea pig cytomegalovirus

    Antimicrob. Agents Chemother.

    (1988)
  • M. Kende et al.

    Treatment of experimental viral infections with immunomodulators

    Adv. Biosci.

    (1988)
  • Cited by (0)

    Abbreviations used: ALUM, aluminum hydroxide; AO, acridine orange; cpm, counts per minute; FITC, fluorescein isothiocyanate; HPV, human papilloma virus; HSV, herpes simplex virus; Ig, immunoglobulin; IFN, interferon; IL, interleukin; LPS, lipopolysaccharide; mAb, monoclonal antibody; NK, natural killer; OVA, ovalbumin; PBMC, peripheral blood mononuclear cell; Poly I:C, polyinosinic:polycytidylic acid; SI, stimulation index; TNF-α, tumor necrosis factor-α.

    View full text