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A Toll-like receptor recognizes bacterial DNA
Abstract
DNA from bacteria has stimulatory effects on mammalian immune cells, which depend on the presence of unmethylated CpG dinucleotides in the bacterial DNA. In contrast, mammalian DNA has a low frequency of CpG dinucleotides, and these are mostly methylated; therefore, mammalian DNA does not have immuno-stimulatory activity. CpG DNA induces a strong T-helper-1-like inflammatory response. Accumulating evidence has revealed the therapeutic potential of CpG DNA as adjuvants for vaccination strategies for cancer, allergy and infectious diseases. Despite its promising clinical use, the molecular mechanism by which CpG DNA activates immune cells remains unclear. Here we show that cellular response to CpG DNA is mediated by a Toll-like receptor, TLR9. TLR9-deficient (TLR9-/-) mice did not show any response to CpG DNA, including proliferation of splenocytes, inflammatory cytokine production from macrophages and maturation of dendritic cells. TLR9-/- mice showed resistance to the lethal effect of CpG DNA without any elevation of serum pro-inflammatory cytokine levels. The in vivo CpG-DNA-mediated T-helper type-1 response was also abolished in TLR9-/- mice. Thus, vertebrate immune systems appear to have evolved a specific Toll-like receptor that distinguishes bacterial DNA from self-DNA.
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“all of the AAV-induced cytokines and chemokines can be upregulated by activation of TLR9 in the periphery using synthetic CpG-rich oligonucleotides.8,9,10,11,12,52,53,54,55,56,57,58”
From An innate immune response to adeno-associated virus genomes decreases cortical dendritic complexity and disrupts synaptic transmission (2024) · cites this paper as [52]
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“Immature DCs 6 (1) 21 (8) 21 (7) 165 (53) 152 (40) 462 (111) LPS 4 (1) 111 (17) 41 (7) 294 (23) 218 (68) 770 (237) HSPB8 5 (2) 65 (12) 38 (11) 238 (57) 262 (21) 610 (197)”
Pichyangkul, S., Yongvanitchit, K., Kum-Arb, U., Hemmi, H., Akira, S., Krieg, A. Μ., Heppner, D. G., Stewart, V. A., Hasegawa, H., Looareesuwan, S., et al. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.8.4926 · Cited by 280
“TLR9-deficient (TLR9 / ) mice were generated as described previously (11) and backcrossed eight times with C57BL/6 mice.”
BackgroundSelf-citationAnti‐tumour strategies aiming to target tumour‐associated macrophages
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Dual recognition of herpes simplex viruses by TLR2 and TLR9 in dendritic cells
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“10,11 The antiviral imidazoquinoline resiquimod (R848) has been shown to be a TLR7 agonist in mice.”
BackgroundNanoparticles for nasal vaccination
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“Examples of adjuvants that enhance costimulatory signaling by presenting foreign/danger signals are: Freund’s adjuvant, certain oligonucleotide sequences such as CpG, double stranded RNA such as poly I:C, bacterial lipopolysaccarides, monophosphoryl lipid A, and mannose [76-79].”
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“Canonically, TLR9 is able to recognize unmethylated CpG motifs on double-stranded DNA from viruses such as HPV [156], EBV [157], and HSV [158].”
BackgroundInfluentialThe Cyclopeptide Astin C Specifically Inhibits the Innate Immune CDN Sensor STING
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“Therefore, new and effective adjuvants may arise from a screen of materials that stimulate the function of APCs, including ganglioside GM1 and ligands of several TLRs (18,22-29).”
BackgroundInfluentialPaget, C., Mallevaey, T., Speak, A. O., Torres, D., Fontaine, J., Sheehan, K. C. F., Capron, M., Ryffel, B., Faveeuw, C., Leite‐de‐Moraes, M., et al. (2007) · Immunity · doi:10.1016/j.immuni.2007.08.017 · Cited by 276
“mice C57BL/6 mice has been described earlier ( Hemmi et al., 2000, 2002; Muller et al., 1994).”
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“This finding led to the proposal that the unmethylated CpG motif that is abundant in the bacterial genome is responsible for the induction of innate immunity by DNA (10); and, this idea was supported by the observation that TLR9 recognizes this DNA motif (20).”
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“Using virus-like particles (VLPs)(2) loaded either with RNA, recognized by TLR7 (33), or CpG DNA, recognized by TLR9 (34), we demonstrate that the critical factor for the induction of IgG2a Abs against VLPs was not Th1 or Th2 cytokines.”
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“TLR9 is bound by unmethylated CpG dinucleotides in bacterial DNA.(119) TLR11 responds specifically to uropathogenic bacteria but not to any of the other known TLR ligands.”
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“Thus, the roles of, for example, TLR6 and TLR1, which can form heterodimers with TLR2 for optimal detection of some Gram-positive PAMPs (18, 45), and TLR9, which recognizes bacterial DNA (46), in S.”
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Metadata
- Authors
- Hemmi, H., Takeuchi, O., Kawai, T., Kaisho, T., Sato, S., Sanjo, H., Matsumoto, M., Hoshino, K., Wagner, H., Takeda, K., & Akira, S.
- Affiliations
- Research Institute for Microbial Diseases, The University of Osaka (JP)
- Japan Science and Technology Agency (JP)
- Technical University of Munich (DE)
- Corresponding author
- Akira, Shizuo
- ORCID
- Venue
- Nature
- Published
- 2000-12-07
- Volume
- 408
- Issue
- 6813
- Pages
- 740-745
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1514540900
- Cited by
- 6,491
- References
- 33
- Citations by year
- 2026: 85 · 2025: 115 · 2024: 136 · 2023: 167 · 2022: 156 · 2021: 191 · 2020: 180 · 2019: 164 · 2018: 187 · 2017: 219 · 2016: 201 · 2015: 226 · 2014: 276 · 2013: 281 · 2012: 235
- FWCI
- 102.08
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Japan Society for the Promotion of Science
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- TLR9, CpG, innate immunity, T helper 1 response, adjuvants, vaccination, dendritic cell maturation, macrophage cytokine production, self-DNA, TLR9-deficient mice
- MeSH terms
- Amino Acid Sequence, Animals, Antigens, Differentiation, Base Sequence, Cells, Cultured, Cloning, Molecular, Dendritic Cells, DNA-Binding Proteins, DNA, Bacterial, T-Lymphocytes, Helper-Inducer, Humans, Membrane Glycoproteins, Mice, Inbred C57BL, Molecular Sequence Data, Receptors, Cell Surface, Receptors, Immunologic, Dinucleoside Phosphates, Signal Transduction, Cytokines, Mutagenesis, Sequence Homology, Amino Acid, Drosophila Proteins, Adaptor Proteins, Signal Transducing, Toll-Like Receptors, Toll-Like Receptor 9, Mice, Myeloid Differentiation Factor 88
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