Rethinking inflammation: neural circuits in the regulation of immunity

Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation

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Host-Bacterial Mutualism in the Human Intestine

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Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin

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Ingestion of <i>Lactobacillus</i> strain regulates emotional behavior and central GABA receptor expression in a mouse via the vagus nerve

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The inflammatory reflex

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Nicotinic acetylcholine receptor α7 subunit is an essential regulator of inflammation

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Baroreflex sensitivity and heart-rate variability in prediction of total cardiac mortality after myocardial infarction

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The Sympathetic Nerve—An Integrative Interface between Two Supersystems: The Brain and the Immune System

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Resolvins

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Enhancing CD8 T-cell memory by modulating fatty acid metabolism

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Acetylcholine-Synthesizing T Cells Relay Neural Signals in a Vagus Nerve Circuit

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Mitochondrial respiratory capacity is a critical regulator of CD8+ T cell memory development

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Functional and chemical anatomy of the afferent vagal system

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Harmful molecular mechanisms in sepsis

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Reflex control of immunity

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Cytokines for psychologists: Implications of bidirectional immune-to-brain communication for understanding behavior, mood, and cognition.

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Has the Microbiota Played a Critical Role in the Evolution of the Adaptive Immune System?

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Stimulation of the vagus nerve attenuates macrophage activation by activating the Jak2-STAT3 signaling pathway

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The Role of Endothelium in the Responses of Vascular Smooth Muscle to Drugs

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Sickness behavior as a new target for drug development

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Fuel feeds function: energy metabolism and the T-cell response

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The cholinergic anti-inflammatory pathway: a missing link in neuroimmunomodulation

Pavlov, V. A., Wang, H., Czura, C. J., Friedman, S. G., & Tracey, K. J. (2003) · Molecular Medicine · doi:10.1007/bf03402177 · Cited by 772 · see citing works

Splenic nerve is required for cholinergic antiinflammatory pathway control of TNF in endotoxemia

Rosas‐Ballina, M., Ochani, M., Parrish, W. R., Ochani, K., Harris, Y., Huston, J. M., Chavan, S. S., & Tracey, K. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803237105 · Cited by 757 · see citing works

Splenectomy inactivates the cholinergic antiinflammatory pathway during lethal endotoxemia and polymicrobial sepsis

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The CNS role of Toll-like receptor 4 in innate neuroimmunity and painful neuropathy

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Cytokine-to-brain communication: A review &amp; analysis of alternative mechanisms

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Pharmacological stimulation of the cholinergic antiinflammatory pathway

Bernik, T. R., Friedman, S. G., Ochani, M., DiRaimo, R., Ulloa, L., Yang, H., Sudan, S., Czura, C. J., Ivanova, S. M., & Tracey, K. J. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20011714 · Cited by 529 · see citing works

Thematic Review Series: Glycerolipids. Phosphatidylcholine and choline homeostasis Published, JLR Papers in Press, January 19, 2008.

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Vagal immune-to-brain communication: a visceral chemosensory pathway

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Blockade of interleukin-1 induced hyperthermia by subdiaphragmatic vagotomy: evidence for vagal mediation of immune-brain communication

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Cholinergic stimulation blocks endothelial cell activation and leukocyte recruitment during inflammation

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Peyer's Patches: The Immune Sensors of the Intestine

Jung, C., Hugot, J., & Barreau, F. (2010) · International Journal of Inflammation · doi:10.4061/2010/823710 · Cited by 467 · see citing works

TLR-dependent T cell activation in autoimmunity

Mills, K. H. G. (2011) · Nature reviews. Immunology · doi:10.1038/nri3095 · Cited by 439 · see citing works

Brain acetylcholinesterase activity controls systemic cytokine levels through the cholinergic anti-inflammatory pathway

Pavlov, V. A., Parrish, W. R., Rosas‐Ballina, M., Ochani, M., Gallowitsch‐Puerta, M., Ochani, K., Chavan, S. S., Al‐Abed, Y., & Tracey, K. J. (2008) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2008.06.011 · Cited by 437 · see citing works

Initial phase 2 trial of a nicotinic agonist in schizophrenia

Freedman, R., Olincy, A., Buchanan, R. W., Harris, J. G., Gold, J. M., Johnson, L., Allensworth, D., Guzman-Bonilla, A., Clement, B., Ball, M. P., et al. (2008) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2008.07071135 · Cited by 426 · see citing works

Functional Innervation of Hepatic iNKT Cells Is Immunosuppressive Following Stroke

Wong, C. H. Y., Jenne, C., Lee, W.-Y., Léger, C., & Kubes, P. (2011) · Science · doi:10.1126/science.1210301 · Cited by 424 · see citing works

The Vagus Nerve and Nicotinic Receptors Modulate Experimental Pancreatitis Severity in Mice

van Westerloo, D. J., Giebelen, I. A., Florquin, S., Bruno, M. J., LaRosa, G. J., Ulloa, L., Tracey, K. J., & van der Poll, T. (2006) · Gastroenterology · doi:10.1053/j.gastro.2006.02.022 · Cited by 377 · see citing works

Activation of Vagal Afferents after Intravenous Injection of Interleukin-1β: Role of Endogenous Prostaglandins

Ek, M., Kurosawa, M., Lundeberg, T., & Ericsson, A. B. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-22-09471.1998 · Cited by 370 · see citing works

Selective parasympathetic innervation of subcutaneous and intra-abdominal fat — functional implications

Kreier, F., Fliers, E., Voshol, P. J., van Eden, C. G., Havekes, L. M., Kalsbeek, A., Heijningen, C. L. V., Sluiter, A. A., Mettenleiter, T. C., Romijn, J. A., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15736 · Cited by 363 · see citing works

Selective α7-nicotinic acetylcholine receptor agonist GTS-21 improves survival in murine endotoxemia and severe sepsis*

Pavlov, V. A., Ochani, M., Yang, L., Gallowitsch‐Puerta, M., Ochani, K., Lin, X., Levi, J., Parrish, W. R., Rosas‐Ballina, M., Czura, C. J., et al. (2007) · Critical Care Medicine · doi:10.1097/01.ccm.0000259381.56526.96 · Cited by 353 · see citing works

Central muscarinic cholinergic regulation of the systemic inflammatory response during endotoxemia

Pavlov, V. A., Ochani, M., Gallowitsch-Puerta, M., Ochani, K., Huston, J. M., Czura, C. J., Al-Abed, Y., & Tracey, K. J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600506103 · Cited by 336 · see citing works

Noradrenergic sympathetic innervation of the spleen: II. Tyrosine hydroxylase (TH)‐positive nerve terminals form synapticlike contacts on lymphocytes in the splenic white pulp

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Selective parasympathetic innervation of subcutaneous and intra-abdominal fat — functional implications

Kreier, F., Fliers, E., Voshol, P. J., van Eden, C. G., Havekes, L. M., Kalsbeek, A., Heijningen, C. L. V., Sluiter, A. A., Mettenleiter, T. C., Romijn, J. A., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215736 · Cited by 331 · see citing works

Choline Transport for Phospholipid Synthesis

Michel, V., Yuan, Z.-F., Ramsubir, S., & Bakovic, M. (2006) · Experimental biology and medicine · doi:10.1177/153537020623100503 · Cited by 330 · see citing works

Modulation of TNF Release by Choline Requires α7 Subunit Nicotinic Acetylcholine Receptor-Mediated Signaling

Parrish, W. R., Rosas‐Ballina, M., Gallowitsch‐Puerta, M., Ochani, M., Ochani, K., Yang, L., Hudson, L., Lin, X., Patel, N. B., Johnson, S. M., et al. (2008) · Molecular Medicine · doi:10.2119/2008-00079.parrish · Cited by 328 · see citing works

Role of vagus nerve signaling in CNI-1493-mediated suppression of acute inflammation

Borovikova, L. V., Ivanova, S., Nardi, D., Zhang, M., Yang, H., Ombrellino, M., & Tracey, K. J. (2000) · Autonomic Neuroscience · doi:10.1016/s1566-0702(00)00233-2 · Cited by 322 · see citing works

Efferent Vagal Fibre Stimulation Blunts Nuclear Factor-κB Activation and Protects Against Hypovolemic Hemorrhagic Shock

Guarini, S., Altavilla, D., Cainazzo, M.-M., Giuliani, D., Bigiani, A., Marini, H., Squadrito, G., Minutoli, L., Bertolini, A., Marini, R., et al. (2003) · Circulation · doi:10.1161/01.cir.0000050627.90734.ed · Cited by 315 · cited 1× · see citing works

Anti-inflammatory effect of vagus nerve stimulation in a rat model of inflammatory bowel disease

Meregnani, J., Clarençon, D., Vivier, M., Peinnequin, A., Mouret, C., Sinniger, V., Picq, C., Job, A., Canini, F., Jacquier-Sarlin, M., et al. (2011) · Autonomic Neuroscience · doi:10.1016/j.autneu.2010.10.007 · Cited by 310 · see citing works

Regional neural activation defines a gateway for autoreactive T cells to cross the blood-brain barrier

Arima, Y., Harada, M., Kamimura, D., Park, J.-H., Kawano, F., Yull, F. E., Kawamoto, T., Iwakura, Y., Betz, U. A. K., Márquez, G., et al. (2012) · Cell · doi:10.1016/j.cell.2012.01.022 · Cited by 307 · see citing works

Transcutaneous vagus nerve stimulation reduces serum high mobility group box 1 levels and improves survival in murine sepsis *

Huston, J. M., Gallowitsch‐Puerta, M., Ochani, M., Ochani, K., Yuan, R., Rosas‐Ballina, M., Ashok, M., Goldstein, R. S., Chavan, S. S., Pavlov, V. A., et al. (2007) · Critical Care Medicine · doi:10.1097/01.ccm.0000288102.15975.ba · Cited by 306 · see citing works

Nutritional stimulation of cholecystokinin receptors inhibits inflammation via the vagus nerve

Luyer, M. D., Greve, J. W. M., Hadfoune, M., Jacobs, J. A., Dejong, C. H., & Buurman, W. A. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20042397 · Cited by 295 · see citing works

Neuronal GPCR Controls Innate Immunity by Regulating Noncanonical Unfolded Protein Response Genes

Sun, J., Singh, V., Kajino‐Sakamoto, R., & Aballay, A. (2011) · Science · doi:10.1126/science.1203411 · Cited by 288 · see citing works

Autonomic dysfunction predicts mortality in patients with multiple organ dysfunction syndrome of different age groups*

Schmidt, H., Müller‐Werdan, U., Hoffmann, T., Francis, D. P., Piepoli, M. F., Rauchhaus, M., Prondzinsky, R., Loppnow, H., Buerke, M., Hoyer, D., et al. (2005) · Critical Care Medicine · doi:10.1097/01.ccm.0000178181.91250.99 · Cited by 275 · see citing works

Stimulation of nicotinic acetylcholine receptors attenuates collagen‐induced arthritis in mice

van Maanen, M. A., Lebre, M. C., van der Poll, T., LaRosa, G. J., Elbaum, D., Vervoordeldonk, M. J., & Tak, P. P. (2008) · Arthritis & Rheumatism · doi:10.1002/art.24177 · Cited by 274 · see citing works

The afferent discharges from sensors for interleukin 1β in the hepatoportal system in the anesthetized rat

Niijima, A. (1996) · Journal of the Autonomic Nervous System · doi:10.1016/s0165-1838(96)00098-7 · Cited by 261 · see citing works

Expression of non-neuronal acetylcholine in lymphocytes and its contribution to the regulation of immune function

Kawashima, K. (2004) · Frontiers in bioscience · doi:10.2741/1390 · Cited by 260 · see citing works

α7-Cholinergic Receptor Mediates Vagal Induction of Splenic Norepinephrine

Vida, G., Peña, G., Deitch, E. A., & Ulloa, L. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1003722 · Cited by 257 · see citing works

Implications of immune-to-brain communication for sickness and pain

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Genomic Organization and Partial Duplication of the Human α7 Neuronal Nicotinic Acetylcholine Receptor Gene (CHRNA7)

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The presence of histamine and acetylcholine in the spleen of the ox and the horse

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Safety, Pharmacokinetics, and Effects on Cognitive Function of Multiple Doses of GTS-21 in Healthy, Male Volunteers

KITAGAWA, H., TAKENOUCHI, T., Azuma, R., Wesnes, K. A., Kramer, W. G., Clody, D. E., & Burnett, A. L. (2002) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300028 · Cited by 238 · see citing works

Expression and function of genes encoding cholinergic components in murine immune cells

Kawashima, K., Yoshikawa, K., Fujii, Y. X., Moriwaki, Y., & Misawa, H. (2007) · Life Sciences · doi:10.1016/j.lfs.2007.02.036 · Cited by 236 · see citing works

Cholinergic antiinflammatory pathway inhibition of tumor necrosis factor during ischemia reperfusion

Bernik, T. R., Friedman, S. G., Ochani, M., DiRaimo, R., Susarla, S., Czura, C. J., & Tracey, K. J. (2002) · Journal of Vascular Surgery · doi:10.1067/mva.2002.129643 · Cited by 228 · see citing works

Activation of the Cholinergic Anti-Inflammatory Pathway Ameliorates Postoperative Ileus in Mice

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Novel pathway for LPS-induced afferent vagus nerve activation: Possible role of nodose ganglion

Hosoi, T., Okuma, Y., Matsuda, T., & Nomura, Y. (2005) · Autonomic Neuroscience · doi:10.1016/j.autneu.2004.11.012 · Cited by 223 · see citing works

The α7 nicotinic acetylcholine receptor in neuronal plasticity

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Inflammation, endothelial dysfunction, and the risk of high blood pressure: epidemiologic and biological evidence

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Cholinergic Anti-Inflammatory Pathway Activity and High Mobility Group Box-1 (HMGB1) Serum Levels in Patients with Rheumatoid Arthritis

Goldstein, R. S., Bruchfeld, A. N., Yang, L., Qureshi, A. R., Gallowitsch‐Puerta, M., Patel, N. B., Huston, B. J., Chavan, S. S., Rosas‐Ballina, M., Gregersen, P. K., et al. (2007) · Molecular Medicine · doi:10.2119/2006-00108.goldstein · Cited by 187 · see citing works

Characterization of vagal innervation to the rat celiac, suprarenal and mesenteric ganglia

Berthoud, H., & Powley, T. L. (1993) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(93)90046-w · Cited by 173 · see citing works

β2‐Adrenoreceptors of regulatory lymphocytes are essential for vagal neuromodulation of the innate immune system

Vida, G., Peña, G., Kanashiro, A., Thompson-Bonilla, M. D. R., Palange, D., Deitch, E. A., & Ulloa, L. (2011) · The FASEB Journal · doi:10.1096/fj.11-191007 · Cited by 167 · see citing works

α7 Nicotinic Acetylcholine Receptor (α7nAChR) Expression in Bone Marrow-Derived Non-T Cells Is Required for the Inflammatory Reflex

Olofsson, P. S., Katz, D. A., Rosas‐Ballina, M., Levine, Y. A., Ochani, M., Valdés‐Ferrer, S. I., Pavlov, V. A., Tracey, K. J., & Chavan, S. S. (2011) · Molecular Medicine · doi:10.2119/molmed.2011.00405 · Cited by 163 · see citing works

Enteric neural crest-derived cells: Origin, identification, migration, and differentiation

Young, H. M., & Newgreen, D. F. (2001) · The Anatomical Record · doi:10.1002/1097-0185(20010101)262:1 · Cited by 163 · see citing works

Antinociceptive effects of tumor necrosis factor α neutralization in a rat model of antigen‐induced arthritis: Evidence of a neuronal target

Boettger, M. K., Hensellek, S., Richter, F., Gajda, M. R., Stöckigt, R., von Banchet, G. S., Bräuer, R., & Schaible, H. (2008) · Arthritis & Rheumatism · doi:10.1002/art.23608 · Cited by 160 · see citing works

Pharmacologic cholinesterase inhibition improves survival in experimental sepsis*

Hofer, S., Eisenbach, C., Lukić, I. K., Schneider, L., Bode, K. A., Brueckmann, M., Mautner, S., Wente, M. N., Encke, J., Werner, J. M., et al. (2008) · Critical Care Medicine · doi:10.1097/01.ccm.0b013e31816208b3 · Cited by 156 · see citing works

Cholinergic agonists attenuate renal ischemia–reperfusion injury in rats

Yeboah, M. M., Xue, X., Duan, B., Ochani, M., Tracey, K. J., Susin, M., & Metz, C. N. (2008) · Kidney International · doi:10.1038/ki.2008.94 · Cited by 150 · see citing works

Interleukin-1 induces c-Fos immunoreactivity in primary afferent neurons of the vagus nerve

Goehler, L. E., Gaykema, R. P. A., Hammack, S. E., Maier, S. F., & Watkins, L. R. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00685-4 · Cited by 146 · see citing works

The effects of interleukin-1β on the activity of adrenal, splenic and renal sympathetic nerves in the rat

Niijima, A., Hori, T., Aou, S., & Oomura, Y. (1991) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(91)90042-2 · Cited by 141 · see citing works

Immunochemical and immunocytochemical characterization of cholinergic markers in human peripheral blood lymphocytes

Tayebati, S. K., El-Assouad, D., Rícci, A., & Amenta, F. (2002) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(02)00325-9 · Cited by 131 · see citing works

Cholinergic Neural Signals to the Spleen Down-Regulate Leukocyte Trafficking via CD11b

Huston, J. M., Rosas‐Ballina, M., Xue, X., Dowling, O., Ochani, K., Ochani, M., Yeboah, M. M., Chatterjee, P. K., Tracey, K. J., & Metz, C. N. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802684 · Cited by 129 · see citing works

Gene expression of mouse choline acetyltransferase. Alternative splicing and identification of a highly active promoter region.

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Function of Partially Duplicated Human α7 Nicotinic Receptor Subunit CHRFAM7A Gene

de Lucas‐Cerrillo, A. M., Maldifassi, M. C., Arnalich, F., Renart, J., Atienza, G., Serantes, R., Cruces, J., Sánchez‐Pacheco, A., Andrés‐Mateos, E., & Montiel, C. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.180067 · Cited by 123 · see citing works

The chimeric gene CHRFAM7A, a partial duplication of the CHRNA7 gene, is a dominant negative regulator of α7*nAChR function

Araud, T., Graw, S. L., Berger, R., Lee, M., Neveu, E., Bertrand, D., & Leonard, S. S. (2011) · Biochemical Pharmacology · doi:10.1016/j.bcp.2011.06.018 · Cited by 122 · see citing works

Stimulated Production of Proinflammatory Cytokines Covaries Inversely With Heart Rate Variability

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Acetylcholinesterase Inhibition Attenuates the Development of Hypertension and Inflammation in Spontaneously Hypertensive Rats

Lataro, R. M., Silva, C. A. A., Tefé‐Silva, C., Prado, C. M., & Salgado, H. C. (2015) · American Journal of Hypertension · doi:10.1093/ajh/hpv017 · Cited by 71 · see citing works

Sleep disruption induces activation of inflammation and heightens risk for infectious disease: Role of impairments in thermoregulation and elevated ambient temperature

Irwin, M. R. (2022) · Temperature · doi:10.1080/23328940.2022.2109932 · Cited by 76 · see citing works

Neuroimmune Modulation Through Vagus Nerve Stimulation Reduces Inflammatory Activity in Crohn’s Disease Patients: A Prospective Open-label Study

D’Haens, G., Eberhardson, M., Čabrijan, Ž., Danese, S., van den Berg, R., Löwenberg, M., Fiorino, G., Schuurman, P. R., Lind, G., Almqvist, P. M., et al. (2023) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjad151 · Cited by 68 · see citing works

An Effective Method for Acute Vagus Nerve Stimulation in Experimental Inflammation

Caravaca, A. S., Gallina, A. L., Tarnawski, L., Tracey, K. J., Pavlov, V. A., Levine, Y. A., & Olofsson, P. S. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00877 · Cited by 68 · see citing works

Causes and Consequences of Degeneration of the Dorsal Motor Nucleus of the Vagus Nerve in Parkinson's Disease

Greene, J. G. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2014.5859 · Cited by 66 · see citing works

A Neuroinflammatory Model for Acute Fatigue During Exercise

Vargas, N. T., & Marino, F. E. (2014) · Sports Medicine · doi:10.1007/s40279-014-0232-4 · Cited by 65 · see citing works

Microbiome to Brain: Unravelling the Multidirectional Axes of Communication

Aidy, S. E., Stilling, R. M., Dinan, T. G., & Cryan, J. F. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-20215-0_15 · Cited by 64 · see citing works

Nicotine Attenuates Osteoarthritis Pain and Matrix Metalloproteinase-9 Expression via the α7 Nicotinic Acetylcholine Receptor

Teng, P., Liu, Y., Dai, Y., Zhang, H., Liu, W., & Hu, J. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1801513 · Cited by 63 · see citing works

Towards a Better Understanding of the Complexities of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and Long COVID

Tate, W. P., Walker, M., Peppercorn, K., Blair, A., & Edgar, C. D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065124 · Cited by 60 · see citing works

Nicotinic ACh receptors in the hippocampal circuit; functional expression and role in synaptic plasticity

Yakel, J. L. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.273896 · Cited by 60 · see citing works

Fetal cholinergic anti-inflammatory pathway and necrotizing enterocolitis: the brain-gut connection begins in utero

Garzoni, L., Faure, C. C., & Frasch, M. G. (2013) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2013.00057 · Cited by 58 · see citing works

A novel flexible cuff-like microelectrode for dual purpose, acute and chronic electrical interfacing with the mouse cervical vagus nerve

Caravaca, A. S., Tsaava, T., Goldman, L., Silverman, H., Riggott, G., Chavan, S. S., Bouton, C., Tracey, K. J., Desimone, R., Boyden, E. S., et al. (2017) · Journal of Neural Engineering · doi:10.1088/1741-2552/aa7a42 · Cited by 57 · see citing works

Neural Control of Inflammation

Steinberg, B. E., Sundman, E., Terrando, N., Eriksson, L. I., & Olofsson, P. S. (2016) · Anesthesiology · doi:10.1097/aln.0000000000001083 · Cited by 57 · see citing works

Reflex principles of immunological homeostasis

Andersson, U., & Tracey, K. J. (2012) · Annual Review of Immunology · doi:10.1146/annurev-immunol-020711-075015 · Cited by 414 · see citing works

Advances in Inflammatory Reflex

Tian, Y. (2009) · Xiandai shengwu yixue jinzhan

From CNI-1493 to the immunological homunculus: physiology of the inflammatory reflex

Oke, S. L., & Tracey, K. J. (2007) · Journal of Leukocyte Biology · doi:10.1189/jlb.0607363 · Cited by 67 · see citing works

Acetylcholine-Synthesizing T Cells Relay Neural Signals in a Vagus Nerve Circuit

Rosas-Ballina, M., Olofsson, P. S., Ochani, M., Valdés-Ferrer, S. I., Levine, Y. A., Reardon, C., Tusche, M. W., Pavlov, V. A., Andersson, U., Chavan, S., et al. (2011) · Science · doi:10.1126/science.1209985 · Cited by 1,551 · see citing works

Nerves and immunity: reflexes in immunological homeostasis (84.2)

Tracey, K. J. (2014) · The FASEB Journal · doi:10.1096/fasebj.28.1_supplement.84.2