(en) Ian Sabroe, Elizabeth C. Jones, Lynne R. Usher et Moira K. B. Whyte, « Toll-Like Receptor (TLR)2 and TLR4 in Human Peripheral Blood Granulocytes: A Critical Role for Monocytes in Leukocyte Lipopolysaccharide Responses », The Journal of Immunology, vol. 168, no 9, , p. 4701–4710 (ISSN0022-1767 et 1550-6606, DOI10.4049/jimmunol.168.9.4701, lire en ligne, consulté le )
(en) Céline Vaure et Yuanqing Liu, « A Comparative Review of Toll-Like Receptor 4 Expression and Functionality in Different Animal Species », Frontiers in Immunology, vol. 5, (ISSN1664-3224, DOI10.3389/fimmu.2014.00316, lire en ligne, consulté le )
(en) Karsten Mahnke, Eva Becher, Paola Ricciardi-Castagnoli et Thomas A. Luger, « CD14 is Expressed by Subsets of Murine Dendritic Cells and Upregulated by Lipopolysaccharide », dans Dendritic Cells in Fundamental and Clinical Immunology: Volume 3, Springer US, , 145–159 p. (ISBN978-1-4757-9966-8, DOI10.1007/978-1-4757-9966-8_25, lire en ligne)
(en) Ian Sabroe, Elizabeth C. Jones, Lynne R. Usher et Moira K. B. Whyte, « Toll-Like Receptor (TLR)2 and TLR4 in Human Peripheral Blood Granulocytes: A Critical Role for Monocytes in Leukocyte Lipopolysaccharide Responses », The Journal of Immunology, vol. 168, no 9, , p. 4701–4710 (ISSN0022-1767 et 1550-6606, DOI10.4049/jimmunol.168.9.4701, lire en ligne, consulté le )
(en) Dianhua Jiang, Jiurong Liang, Juan Fan et Shuang Yu, « Regulation of lung injury and repair by Toll-like receptors and hyaluronan », Nature Medicine, vol. 11, no 11, , p. 1173–1179 (ISSN1546-170X, DOI10.1038/nm1315, lire en ligne, consulté le )
(en) Hongliang Fang, Bing Ang, Xinyun Xu et Xiaohui Huang, « TLR4 is essential for dendritic cell activation and anti-tumor T-cell response enhancement by DAMPs released from chemically stressed cancer cells », Cellular & Molecular Immunology, vol. 11, no 2, , p. 150–159 (ISSN2042-0226, DOI10.1038/cmi.2013.59, lire en ligne, consulté le )
« A comparative review of toll-like receptor 4 expression and functionality in different animal species », Frontiers in Immunology, vol. 5, , p. 316 (PMID25071777, PMCID4090903, DOI10.3389/fimmu.2014.00316)
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« Different selective pressures shape the evolution of Toll-like receptors in human and African great ape populations », Human Molecular Genetics, vol. 22, no 23, , p. 4829–40 (PMID23851028, PMCID3820138, DOI10.1093/hmg/ddt335)
« The evolutionary history of TLR4 polymorphisms in Europe », Journal of Innate Immunity, vol. 4, no 2, , p. 168–75 (PMID21968286, DOI10.1159/000329492)
« Monomeric recombinant MD-2 binds toll-like receptor 4 tightly and confers lipopolysaccharide responsiveness », The Journal of Biological Chemistry, vol. 277, no 26, , p. 23427–32 (PMID11976338, DOI10.1074/jbc.M202554200)
« MD-2, a molecule that confers lipopolysaccharide responsiveness on Toll-like receptor 4 », The Journal of Experimental Medicine, vol. 189, no 11, , p. 1777–82 (PMID10359581, PMCID2193086, DOI10.1084/jem.189.11.1777)
« Triad3A, an E3 ubiquitin-protein ligase regulating Toll-like receptors », Nature Immunology, vol. 5, no 5, , p. 495–502 (PMID15107846, DOI10.1038/ni1066)
« Toll-like receptor 3 mediates a more potent antiviral response than Toll-like receptor 4 », Journal of Immunology, vol. 170, no 7, , p. 3565–71 (PMID12646618, DOI10.4049/jimmunol.170.7.3565)
« Murine TOLL-like receptor 4 confers lipopolysaccharide responsiveness as determined by activation of NF kappa B and expression of the inducible cyclooxygenase », The Journal of Biological Chemistry, vol. 275, no 44, , p. 34035–40 (PMID10952994, DOI10.1074/jbc.M007386200)
« Mal (MyD88-adapter-like) is required for Toll-like receptor-4 signal transduction », Nature, vol. 413, no 6851, , p. 78–83 (PMID11544529, DOI10.1038/35092578)
« Negative regulation of toll-like receptor-mediated signaling by Tollip », The Journal of Biological Chemistry, vol. 277, no 9, , p. 7059–65 (PMID11751856, DOI10.1074/jbc.M109537200)
« The Rab11a GTPase controls Toll-like receptor 4-induced activation of interferon regulatory factor-3 on phagosomes », Immunity, vol. 33, no 4, , p. 583–96 (PMID20933442, DOI10.1016/j.immuni.2010.09.010)
« Single nucleotide polymorphisms of Toll-like receptors and susceptibility to infectious disease », The Lancet. Infectious Diseases, vol. 5, no 3, , p. 156–64 (PMID15766650, DOI10.1016/S1473-3099(05)01308-3)
« Relevance of mutations in the TLR4 receptor in patients with gram-negative septic shock », Archives of Internal Medicine, vol. 162, no 9, , p. 1028–32 (PMID11996613, DOI10.1001/archinte.162.9.1028)
« Polymorphisms of the toll-like receptor 2 and 4 genes are associated with faster progression and a more severe course of sepsis in critically ill patients », The Journal of International Medical Research, vol. 42, no 1, , p. 93–110 (PMID24366499, DOI10.1177/0300060513504358)
« Toll-like receptor (TLR) polymorphisms in African children: Common TLR-4 variants predispose to severe malaria », Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no 1, , p. 177–82 (PMID16371473, PMCID1324982, DOI10.1073/pnas.0506803102)
« Toll-like receptor 4 variant D299G induces features of neoplastic progression in Caco-2 intestinal cells and is associated with advanced human colon cancer », Gastroenterology, vol. 141, no 6, , p. 2154–65 (PMID21920464, PMCID3268964, DOI10.1053/j.gastro.2011.08.043)
« Binge alcohol drinking is associated with GABAA alpha2-regulated Toll-like receptor 4 (TLR4) expression in the central amygdala », Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no 11, , p. 4465–70 (PMID21368176, PMCID3060224, DOI10.1073/pnas.1019020108)
« Involvement of TLR4/type I IL-1 receptor signaling in the induction of inflammatory mediators and cell death induced by ethanol in cultured astrocytes », Journal of Immunology, vol. 175, no 10, , p. 6893–9 (PMID16272348, DOI10.4049/jimmunol.175.10.6893)
« Fragmented sleep accelerates tumor growth and progression through recruitment of tumor-associated macrophages and TLR4 signaling », Cancer Research, vol. 74, no 5, , p. 1329–37 (PMID24448240, PMCID4247537, DOI10.1158/0008-5472.CAN-13-3014)
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« Etanercept restores the antinociceptive effect of morphine and suppresses spinal neuroinflammation in morphine-tolerant rats », Anesthesia and Analgesia, vol. 112, no 2, , p. 454–9 (PMID21081778, DOI10.1213/ANE.0b013e3182025b15)
« An IL-1 receptor antagonist blocks a morphine-induced attenuation of locomotor recovery after spinal cord injury », Brain, Behavior, and Immunity, vol. 25, no 2, , p. 349–59 (PMID20974246, PMCID3025088, DOI10.1016/j.bbi.2010.10.018)
« The "toll" of opioid-induced glial activation: improving the clinical efficacy of opioids by targeting glia », Trends in Pharmacological Sciences, vol. 30, no 11, , p. 581–91 (PMID19762094, PMCID2783351, DOI10.1016/j.tips.2009.08.002)
« Non-stereoselective reversal of neuropathic pain by naloxone and naltrexone: involvement of toll-like receptor 4 (TLR4) », The European Journal of Neuroscience, vol. 28, no 1, , p. 20–9 (PMID18662331, PMCID2588470, DOI10.1111/j.1460-9568.2008.06321.x)
« Possible involvement of toll-like receptor 4/myeloid differentiation factor-2 activity of opioid inactive isomers causes spinal proinflammation and related behavioral consequences », Neuroscience, vol. 167, no 3, , p. 880–93 (PMID20178837, PMCID2854318, DOI10.1016/j.neuroscience.2010.02.011)
« Ultra-low dose naloxone upregulates interleukin-10 expression and suppresses neuroinflammation in morphine-tolerant rat spinal cords », Behavioural Brain Research, vol. 207, no 1, , p. 30–6 (PMID19799935, DOI10.1016/j.bbr.2009.09.034)
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Kelley KW, Dantzer R, « Alcoholism and inflammation: neuroimmunology of behavioral and mood disorders », Brain, Behavior, and Immunity, vol. 25 Suppl 1, , S13-20 (PMID21193024, PMCID4068736, DOI10.1016/j.bbi.2010.12.013)
« Percutaneous penetration of 2,4-dichlorophenoxyacetic acid and 2,4-D dimethylamine salt in human volunteers », Journal of Toxicology and Environmental Health, vol. 36, no 3, , p. 233–40 (PMID1629934, DOI10.1080/15287399209531634)
« Glucuronoxylomannan, a microbial compound, regulates expression of costimulatory molecules and production of cytokines in macrophages », The Journal of Infectious Diseases, vol. 191, no 1, , p. 127–37 (PMID15593014, DOI10.1086/426511)
« Stereoselective action of (+)-morphine over (-)-morphine in attenuating the (-)-morphine-produced antinociception via the naloxone-sensitive sigma receptor in the mouse », European Journal of Pharmacology, vol. 571, nos 2–3, , p. 145–51 (PMID17617400, PMCID2080825, DOI10.1016/j.ejphar.2007.06.012)
« Phase 2 trial of eritoran tetrasodium (E5564), a toll-like receptor 4 antagonist, in patients with severe sepsis », Critical Care Medicine, vol. 38, no 1, , p. 72–83 (PMID19661804, DOI10.1097/CCM.0b013e3181b07b78)
Hutchinson MR, Loram LC, Zhang Y, Shridhar M, Rezvani N, Berkelhammer D, Phipps S, Foster PS, Landgraf K, Falke JJ, Rice KC, Maier SF, Yin H, Watkins LR, « Evidence that tricyclic small molecules may possess toll-like receptor and myeloid differentiation protein 2 activity », Neuroscience, vol. 168, no 2, , p. 551–63 (PMID20381591, PMCID2872682, DOI10.1016/j.neuroscience.2010.03.067)
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Lan X, Han X, Li Q, Li Q, Gao Y, Cheng T, Wan J, Zhu W, Wang J, « Pinocembrin protects hemorrhagic brain primarily by inhibiting toll-like receptor 4 and reducing M1 phenotype microglia », Brain, behavior, and immunity, vol. 61, , p. 326–339 (PMID28007523, PMCID5453178, DOI10.1016/j.bbi.2016.12.012)
Hutchinson MR, Zhang Y, Shridhar M, Evans JH, Buchanan MM, Zhao TX, Slivka PF, Coats BD, Rezvani N, Wieseler J, Hughes TS, Landgraf KE, Chan S, Fong S, Phipps S, Falke JJ, Leinwand LA, Maier SF, Yin H, Rice KC, Watkins LR, « Evidence that opioids may have toll-like receptor 4 and MD-2 effects », Brain, Behavior, and Immunity, vol. 24, no 1, , p. 83–95 (PMID19679181, PMCID2788078, DOI10.1016/j.bbi.2009.08.004)
(en) Céline Vaure et Yuanqing Liu, « A Comparative Review of Toll-Like Receptor 4 Expression and Functionality in Different Animal Species », Frontiers in Immunology, vol. 5, (ISSN1664-3224, DOI10.3389/fimmu.2014.00316, lire en ligne, consulté le )
issn.org
portal.issn.org
(en) Céline Vaure et Yuanqing Liu, « A Comparative Review of Toll-Like Receptor 4 Expression and Functionality in Different Animal Species », Frontiers in Immunology, vol. 5, (ISSN1664-3224, DOI10.3389/fimmu.2014.00316, lire en ligne, consulté le )
(en) Ian Sabroe, Elizabeth C. Jones, Lynne R. Usher et Moira K. B. Whyte, « Toll-Like Receptor (TLR)2 and TLR4 in Human Peripheral Blood Granulocytes: A Critical Role for Monocytes in Leukocyte Lipopolysaccharide Responses », The Journal of Immunology, vol. 168, no 9, , p. 4701–4710 (ISSN0022-1767 et 1550-6606, DOI10.4049/jimmunol.168.9.4701, lire en ligne, consulté le )
(en) Dianhua Jiang, Jiurong Liang, Juan Fan et Shuang Yu, « Regulation of lung injury and repair by Toll-like receptors and hyaluronan », Nature Medicine, vol. 11, no 11, , p. 1173–1179 (ISSN1546-170X, DOI10.1038/nm1315, lire en ligne, consulté le )
(en) Hongliang Fang, Bing Ang, Xinyun Xu et Xiaohui Huang, « TLR4 is essential for dendritic cell activation and anti-tumor T-cell response enhancement by DAMPs released from chemically stressed cancer cells », Cellular & Molecular Immunology, vol. 11, no 2, , p. 150–159 (ISSN2042-0226, DOI10.1038/cmi.2013.59, lire en ligne, consulté le )
jle.com
« Toll-like receptor 4 Asp299Gly/Thr399Ile polymorphisms are a risk factor for Candida bloodstream infection », European Cytokine Network, vol. 17, no 1, , p. 29–34 (PMID16613760, lire en ligne)
nature.com
(en) Dianhua Jiang, Jiurong Liang, Juan Fan et Shuang Yu, « Regulation of lung injury and repair by Toll-like receptors and hyaluronan », Nature Medicine, vol. 11, no 11, , p. 1173–1179 (ISSN1546-170X, DOI10.1038/nm1315, lire en ligne, consulté le )
(en) Hongliang Fang, Bing Ang, Xinyun Xu et Xiaohui Huang, « TLR4 is essential for dendritic cell activation and anti-tumor T-cell response enhancement by DAMPs released from chemically stressed cancer cells », Cellular & Molecular Immunology, vol. 11, no 2, , p. 150–159 (ISSN2042-0226, DOI10.1038/cmi.2013.59, lire en ligne, consulté le )
« A comparative review of toll-like receptor 4 expression and functionality in different animal species », Frontiers in Immunology, vol. 5, , p. 316 (PMID25071777, PMCID4090903, DOI10.3389/fimmu.2014.00316)
« The history of Toll-like receptors - redefining innate immunity », Nature Reviews. Immunology, vol. 13, no 6, , p. 453–60 (PMID23681101, DOI10.1038/nri3446)
« Evolution of the TIR, tolls and TLRs: functional inferences from computational biology », Current Topics in Microbiology and Immunology, vol. 270, , p. 1–21 (PMID12467241)
« Different selective pressures shape the evolution of Toll-like receptors in human and African great ape populations », Human Molecular Genetics, vol. 22, no 23, , p. 4829–40 (PMID23851028, PMCID3820138, DOI10.1093/hmg/ddt335)
« The evolutionary history of TLR4 polymorphisms in Europe », Journal of Innate Immunity, vol. 4, no 2, , p. 168–75 (PMID21968286, DOI10.1159/000329492)
« Monomeric recombinant MD-2 binds toll-like receptor 4 tightly and confers lipopolysaccharide responsiveness », The Journal of Biological Chemistry, vol. 277, no 26, , p. 23427–32 (PMID11976338, DOI10.1074/jbc.M202554200)
« MD-2, a molecule that confers lipopolysaccharide responsiveness on Toll-like receptor 4 », The Journal of Experimental Medicine, vol. 189, no 11, , p. 1777–82 (PMID10359581, PMCID2193086, DOI10.1084/jem.189.11.1777)
« Triad3A, an E3 ubiquitin-protein ligase regulating Toll-like receptors », Nature Immunology, vol. 5, no 5, , p. 495–502 (PMID15107846, DOI10.1038/ni1066)
« Toll-like receptor 3 mediates a more potent antiviral response than Toll-like receptor 4 », Journal of Immunology, vol. 170, no 7, , p. 3565–71 (PMID12646618, DOI10.4049/jimmunol.170.7.3565)
« Murine TOLL-like receptor 4 confers lipopolysaccharide responsiveness as determined by activation of NF kappa B and expression of the inducible cyclooxygenase », The Journal of Biological Chemistry, vol. 275, no 44, , p. 34035–40 (PMID10952994, DOI10.1074/jbc.M007386200)
« Mal (MyD88-adapter-like) is required for Toll-like receptor-4 signal transduction », Nature, vol. 413, no 6851, , p. 78–83 (PMID11544529, DOI10.1038/35092578)
« Negative regulation of toll-like receptor-mediated signaling by Tollip », The Journal of Biological Chemistry, vol. 277, no 9, , p. 7059–65 (PMID11751856, DOI10.1074/jbc.M109537200)
« The Rab11a GTPase controls Toll-like receptor 4-induced activation of interferon regulatory factor-3 on phagosomes », Immunity, vol. 33, no 4, , p. 583–96 (PMID20933442, DOI10.1016/j.immuni.2010.09.010)
« Single nucleotide polymorphisms of Toll-like receptors and susceptibility to infectious disease », The Lancet. Infectious Diseases, vol. 5, no 3, , p. 156–64 (PMID15766650, DOI10.1016/S1473-3099(05)01308-3)
« Relevance of mutations in the TLR4 receptor in patients with gram-negative septic shock », Archives of Internal Medicine, vol. 162, no 9, , p. 1028–32 (PMID11996613, DOI10.1001/archinte.162.9.1028)
« Polymorphisms of the toll-like receptor 2 and 4 genes are associated with faster progression and a more severe course of sepsis in critically ill patients », The Journal of International Medical Research, vol. 42, no 1, , p. 93–110 (PMID24366499, DOI10.1177/0300060513504358)
« Toll-like receptor (TLR) polymorphisms in African children: Common TLR-4 variants predispose to severe malaria », Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no 1, , p. 177–82 (PMID16371473, PMCID1324982, DOI10.1073/pnas.0506803102)
« Toll-like receptor 4 Asp299Gly/Thr399Ile polymorphisms are a risk factor for Candida bloodstream infection », European Cytokine Network, vol. 17, no 1, , p. 29–34 (PMID16613760, lire en ligne)
« Toll-like receptor 4 variant D299G induces features of neoplastic progression in Caco-2 intestinal cells and is associated with advanced human colon cancer », Gastroenterology, vol. 141, no 6, , p. 2154–65 (PMID21920464, PMCID3268964, DOI10.1053/j.gastro.2011.08.043)
« Binge alcohol drinking is associated with GABAA alpha2-regulated Toll-like receptor 4 (TLR4) expression in the central amygdala », Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no 11, , p. 4465–70 (PMID21368176, PMCID3060224, DOI10.1073/pnas.1019020108)
« Involvement of TLR4/type I IL-1 receptor signaling in the induction of inflammatory mediators and cell death induced by ethanol in cultured astrocytes », Journal of Immunology, vol. 175, no 10, , p. 6893–9 (PMID16272348, DOI10.4049/jimmunol.175.10.6893)
« Fragmented sleep accelerates tumor growth and progression through recruitment of tumor-associated macrophages and TLR4 signaling », Cancer Research, vol. 74, no 5, , p. 1329–37 (PMID24448240, PMCID4247537, DOI10.1158/0008-5472.CAN-13-3014)
« Interleukin-1 antagonizes morphine analgesia and underlies morphine tolerance », Pain, vol. 115, nos 1–2, , p. 50–9 (PMID15836969, DOI10.1016/j.pain.2005.02.003)
« Dual regulation of mu opioid receptors in SK-N-SH neuroblastoma cells by morphine and interleukin-1β: evidence for opioid-immune crosstalk », Journal of Neuroimmunology, vol. 227, nos 1–2, , p. 26–34 (PMID20615556, PMCID2942958, DOI10.1016/j.jneuroim.2010.06.007)
« Etanercept restores the antinociceptive effect of morphine and suppresses spinal neuroinflammation in morphine-tolerant rats », Anesthesia and Analgesia, vol. 112, no 2, , p. 454–9 (PMID21081778, DOI10.1213/ANE.0b013e3182025b15)
« An IL-1 receptor antagonist blocks a morphine-induced attenuation of locomotor recovery after spinal cord injury », Brain, Behavior, and Immunity, vol. 25, no 2, , p. 349–59 (PMID20974246, PMCID3025088, DOI10.1016/j.bbi.2010.10.018)
« The "toll" of opioid-induced glial activation: improving the clinical efficacy of opioids by targeting glia », Trends in Pharmacological Sciences, vol. 30, no 11, , p. 581–91 (PMID19762094, PMCID2783351, DOI10.1016/j.tips.2009.08.002)
« Non-stereoselective reversal of neuropathic pain by naloxone and naltrexone: involvement of toll-like receptor 4 (TLR4) », The European Journal of Neuroscience, vol. 28, no 1, , p. 20–9 (PMID18662331, PMCID2588470, DOI10.1111/j.1460-9568.2008.06321.x)
« Possible involvement of toll-like receptor 4/myeloid differentiation factor-2 activity of opioid inactive isomers causes spinal proinflammation and related behavioral consequences », Neuroscience, vol. 167, no 3, , p. 880–93 (PMID20178837, PMCID2854318, DOI10.1016/j.neuroscience.2010.02.011)
« Ultra-low dose naloxone upregulates interleukin-10 expression and suppresses neuroinflammation in morphine-tolerant rat spinal cords », Behavioural Brain Research, vol. 207, no 1, , p. 30–6 (PMID19799935, DOI10.1016/j.bbr.2009.09.034)
Pascual M, Baliño P, Alfonso-Loeches S, Aragón CM, Guerri C, « Impact of TLR4 on behavioral and cognitive dysfunctions associated with alcohol-induced neuroinflammatory damage », Brain, Behavior, and Immunity, vol. 25 Suppl 1, , S80-91 (PMID21352907, DOI10.1016/j.bbi.2011.02.012)
Kelley KW, Dantzer R, « Alcoholism and inflammation: neuroimmunology of behavioral and mood disorders », Brain, Behavior, and Immunity, vol. 25 Suppl 1, , S13-20 (PMID21193024, PMCID4068736, DOI10.1016/j.bbi.2010.12.013)
« Percutaneous penetration of 2,4-dichlorophenoxyacetic acid and 2,4-D dimethylamine salt in human volunteers », Journal of Toxicology and Environmental Health, vol. 36, no 3, , p. 233–40 (PMID1629934, DOI10.1080/15287399209531634)
« Glucuronoxylomannan, a microbial compound, regulates expression of costimulatory molecules and production of cytokines in macrophages », The Journal of Infectious Diseases, vol. 191, no 1, , p. 127–37 (PMID15593014, DOI10.1086/426511)
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Lan X, Han X, Li Q, Li Q, Gao Y, Cheng T, Wan J, Zhu W, Wang J, « Pinocembrin protects hemorrhagic brain primarily by inhibiting toll-like receptor 4 and reducing M1 phenotype microglia », Brain, behavior, and immunity, vol. 61, , p. 326–339 (PMID28007523, PMCID5453178, DOI10.1016/j.bbi.2016.12.012)
Hutchinson MR, Zhang Y, Shridhar M, Evans JH, Buchanan MM, Zhao TX, Slivka PF, Coats BD, Rezvani N, Wieseler J, Hughes TS, Landgraf KE, Chan S, Fong S, Phipps S, Falke JJ, Leinwand LA, Maier SF, Yin H, Rice KC, Watkins LR, « Evidence that opioids may have toll-like receptor 4 and MD-2 effects », Brain, Behavior, and Immunity, vol. 24, no 1, , p. 83–95 (PMID19679181, PMCID2788078, DOI10.1016/j.bbi.2009.08.004)
(en) Karsten Mahnke, Eva Becher, Paola Ricciardi-Castagnoli et Thomas A. Luger, « CD14 is Expressed by Subsets of Murine Dendritic Cells and Upregulated by Lipopolysaccharide », dans Dendritic Cells in Fundamental and Clinical Immunology: Volume 3, Springer US, , 145–159 p. (ISBN978-1-4757-9966-8, DOI10.1007/978-1-4757-9966-8_25, lire en ligne)