scispace - formally typeset
Journal ArticleDOI

Cpg motifs in bacterial dna trigger direct b-cell activation

TLDR
The potent immune activation by CpG oligon nucleotides has impli-cations for the design and interpretation of studies using 'antisense' oligonucleotides and points to possible new applications as adjuvants.
Abstract
Unmethylated CpG dinucleotides are more frequent in the genomes of bacteria and viruses than of vertebrates. We report here that bacterial DNA and synthetic oligodeoxynucleotides containing unmethylated CpG dinucleotides induce murine B cells to proliferate and secrete immunoglobulin in vitro and in vivo. This activation is enhanced by simultaneous signals delivered through the antigen receptor. Optimal B-cell activation requires a DNA motif in which an unmethylated CpG dinucleotide is flanked by two 5' purines and two 3' pyrimidines. Oligodeoxynucleotides containing this CpG motif induce more than 95% of all spleen B cells to enter the cell cycle. These data suggest a possible evolutionary link between immune defence based on the recognition of microbial DNA and the phenomenon of 'CpG suppression' in vertebrates. The potent immune activation by CpG oligonucleotides has implications for the design and interpretation of studies using 'antisense' oligonucleotides and points to possible new applications as adjuvants.

read more

Citations
More filters
Journal ArticleDOI

Innate Immune Recognition

TL;DR: Microbial recognition by Toll-like receptors helps to direct adaptive immune responses to antigens derived from microbial pathogens to distinguish infectious nonself from noninfectious self.
Journal ArticleDOI

A Toll-like receptor recognizes bacterial DNA.

TL;DR: It is shown that cellular response to CpG DNA is mediated by a Toll-like receptor, TLR9, and vertebrate immune systems appear to have evolved a specific Toll- like receptor that distinguishes bacterial DNA from self-DNA.
Journal ArticleDOI

Toll-like receptors.

TL;DR: This unit discusses mammalian Toll receptors (TLR1‐10) that have an essential role in the innate immune recognition of microorganisms and are discussed are TLR‐mediated signaling pathways and antibodies that are available to detect specific TLRs.
Journal ArticleDOI

Toll-like receptors and innate immunity

TL;DR: This work has shown that activation of inflammatory and antimicrobial innate immune responses through recognition of Toll-like receptors expressed on dendritic cells triggers functional maturation of dendrites and leads to initiation of antigen-specific adaptive immune responses.
Journal ArticleDOI

Small anti-viral compounds activate immune cells via the TLR7 MyD88-dependent signaling pathway.

TL;DR: It is shown that the imidazoquinolines activate immune cells via the Toll-like receptor 7 (TLR7)-MyD88–dependent signaling pathway, and that neither MyD88- nor TLR7-deficient mice showed any inflammatory cytokine production by macrophages, proliferation of splenocytes or maturation of dendritic cells.
References
More filters
Journal ArticleDOI

Antisense oligonucleotides as therapeutic agents--is the bullet really magical?

TL;DR: The potential use of phosphorothioate oligos as inhibitors of viral replication is highlighted and these are examples of oligos that are being considered for clinical therapeutic trials and meet some, but not all, of these criteria.
Journal ArticleDOI

Gene inhibition using antisense oligodeoxynucleotides.

Richard W. Wagner
- 24 Nov 1994 - 
TL;DR: Improvements in ODN chemistry and cellular delivery techniques now allow for more potent and specific gene inhibition.
Journal ArticleDOI

CpG islands as gene markers in the vertebrate nucleus

TL;DR: CpG islands are already being used to identify potential genes in isolated DNA, and they may function analogously in vivo, as gene markers for ubiquitous nuclear factors.
Journal ArticleDOI

Pharmacokinetics, biodistribution, and stability of oligodeoxynucleotide phosphorothioates in mice

TL;DR: The surprising observation was made that chain length extension of administered [S]oligonucleotide occurred in kidney, liver, and intestine, which provides an initial definition of parameters for the pharmaceutical development of antisense oligonucleotides.
Related Papers (5)