Intra-articularly localized bacterial DNA containing CpG motifs induces arthritis

GM Deng, IM Nilsson, M Verdrengh, LV Collins… - Nature medicine, 1999 - nature.com
GM Deng, IM Nilsson, M Verdrengh, LV Collins, A Tarkowski
Nature medicine, 1999nature.com
Unmethylated CpG motifs are often found in bacterial DNA, and exert immunostimulatory
effects on hematopoetic cells 1, 2, 3. Bacteria produce severe joint inflammation in septic
and reactive arthritides; bacterial DNA may be involved in this process. We injected bacterial
DNA originating from Escherichia coli and Staphylococcus aureus and oligonucleotides
containing CpG directly into the knee joints of mice of different strains. Arthritis was seen by
histopathology within 2 hours and lasted for at least 14 days. Unmethylated CpG motifs were …
Abstract
Unmethylated CpG motifs are often found in bacterial DNA, and exert immunostimulatory effects on hematopoetic cells 1, 2, 3. Bacteria produce severe joint inflammation in septic and reactive arthritides; bacterial DNA may be involved in this process. We injected bacterial DNA originating from Escherichia coli and Staphylococcus aureus and oligonucleotides containing CpG directly into the knee joints of mice of different strains. Arthritis was seen by histopathology within 2 hours and lasted for at least 14 days. Unmethylated CpG motifs were responsible for this induction of arthritis, as oligonucleotides containing these motifs produced the arthritis. The arthritis was characterized by an influx of monocytic, Mac-1+ cells and by a lack of T lymphocytes. Depletion of monocytes resulted in abrogation of the synovial inflammation. Tumor necrosis factor (TNF)-α, a cytokine produced by cells of the monocyte/macrophage lineage, is an important mediator of this disease, as expression of mRNA for TNF-α was evident in the inflamed joints, and the CpG-mediated inflammation was abrogated in mice genetically unable to produce this cytokine. These findings demonstrate that bacterial DNA containing unmethylated CpG motifs induces arthritis, and indicate an important pathogenic role for bacterial DNA in septic arthritis.
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