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The inflammatory response in sepsis
Open accessAbstract
The pathophysiology of sepsis and its accompanying systemic inflammatory response syndrome (SIRS) and the events that lead to multiorgan failure and death are poorly understood. It is known that, in septic humans and rodents, the development of SIRS is associated with a loss of the redox balance, but SIRS can also develop in non-infectious states. In addition, a hyperinflammatory state develops, together with impaired innate immune functions of phagocytes, immunosuppression, and complement activation, collectively leading to septic shock and lethality. Here we discuss recent insights into the signaling pathways in immune and phagocytic cells that underlie sepsis and SIRS and consider how these might be targeted for therapeutic interventions to reverse or attenuate pathways that lead to lethality during sepsis.
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Cites
Free radicals and antioxidants in normal physiological functions and human disease
Valko, M., Leibfritz, D., Moncol, J., Cronin, M. T. D., Mazur, M., & Telser, J. (2007) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2006.07.001 · Cited by 14,269
The epidemiology of sepsis in the United States from 1979 through 2000
Martin, G. S., Mannino, D. M., Eaton, S., & Moss, M. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa022139 · Cited by 5,841
Immunodesign of experimental sepsis by cecal ligation and puncture
Rittirsch, D., Huber-Lang, M. S., Flierl, M. A., & Ward, P. A. (2009) · Nature Protocols · doi:10.1038/nprot.2008.214 · Cited by 2,209
Self-citationImmunosuppression in Patients Who Die of Sepsis and Multiple Organ Failure
Boomer, J. S., To, K., Chang, K. C., Takasu, O., Osborne, D. F., Walton, A. H., Bricker, T. L., Jarman, S. D., Kreisel, D., Krupnick, A. S., et al. (2011) · JAMA · doi:10.1001/jama.2011.1829 · Cited by 1,781
The acute respiratory distress syndrome
Matthay, M. A., Ware, L. B., & Zimmerman, G. A. (2012) · Journal of Clinical Investigation · doi:10.1172/jci60331 · Cited by 1,706
Cecal ligation and puncture: the gold standard model for polymicrobial sepsis?
Dejager, L., Pinheiro, I., Dejonckheere, E., & Libert, C. (2011) · Trends in Microbiology · doi:10.1016/j.tim.2011.01.001 · Cited by 784
Animal models of sepsis and sepsis-induced kidney injury
Doi, K., Leelahavanichkul, A., Yuen, P. S. T., & Star, R. A. (2009) · Journal of Clinical Investigation · doi:10.1172/jci39421 · Cited by 580
The sepsis seesaw: tilting toward immunosuppression
Hotchkiss, R. S., Coopersmith, C. M., McDunn, J. E., & Ferguson, T. A. (2009) · Nature Medicine · doi:10.1038/nm0509-496 · Cited by 574
Antidiabetic actions of a non-agonist PPARγ ligand blocking Cdk5-mediated phosphorylation
Choi, J. H., Banks, A. S., Kamenecka, T. M., Busby, S. A., Chalmers, M. J., Kumar, N., Kuruvilla, D. S., Shin, Y., He, Y., Bruning, J. B., et al. (2011) · Nature · doi:10.1038/nature10383 · Cited by 536
Endogenous ligands of TLR2 and TLR4: agonists or assistants?
Erridge, C. (2010) · Journal of Leukocyte Biology · doi:10.1189/jlb.1209775 · Cited by 518
Nrf2: friend or foe for chemoprevention?
Kensler, T. W., & Wakabayashi, N. (2010) · Carcinogenesis · doi:10.1093/carcin/bgp231 · Cited by 484
Phagocyte-derived catecholamines enhance acute inflammatory injury
Flierl, M. A., Rittirsch, D., Nadeau, B. A., Chen, A. J., Sarma, J. V., Zetoune, F. S., McGuire, S. R., List, R. P., Day, D. E., Hoesel, L. M., et al. (2007) · Nature · doi:10.1038/nature06185 · Cited by 475
Self-citationHydroxyl Radical and Its Scavengers in Health and Disease
Lipinski, B. (2011) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2011/809696 · Cited by 456
INTESTINAL CROSSTALK: A NEW PARADIGM FOR UNDERSTANDING THE GUT AS THE "MOTOR" OF CRITICAL ILLNESS
Clark, J. A., & Coopersmith, C. M. (2007) · Shock · doi:10.1097/shk.0b013e31805569df · Cited by 444
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
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
IL-7 Promotes T Cell Viability, Trafficking, and Functionality and Improves Survival in Sepsis
Unsinger, J., McGlynn, M., Kasten, K. R., Hoekzema, A. S., Watanabe, E., Muenzer, J. T., McDonough, J. S., Tschoep, J., Ferguson, T. A., McDunn, J. E., et al. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903151 · Cited by 312
Animal models of sepsis: Why does preclinical efficacy fail to translate to the clinical setting?
Dyson, A., & Singer, M. (2009) · Critical Care Medicine · doi:10.1097/ccm.0b013e3181922bd3 · Cited by 273
The Search for Effective Therapy for Sepsis: Back to the Drawing Board?
Angus, D. C. (2011) · JAMA · doi:10.1001/jama.2011.1853 · Cited by 264
The C5a Receptor (C5aR) C5L2 Is a Modulator of C5aR-mediated Signal Transduction
Bamberg, C. E., Mackay, C. R., Lee, H., Zahra, D., Jackson, J., Lim, Y. S., Whitfeld, P. L., Craig, S., Corsini, E., Lu, B., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.092106 · Cited by 249
Activation of Nrf2 in Endothelial Cells Protects Arteries From Exhibiting a Proinflammatory State
Zakkar, M., Van der Heiden, K., Luong, L. A., Chaudhury, H., Cuhlmann, S., Hamdulay, S. S., Krams, R., Edirisinghe, I., Rahman, I., Carlsen, H., et al. (2009) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.109.193375 · Cited by 247
PPAR and Oxidative Stress: Con() Catenating NRF2 and FOXO
Polvani, S., Tarocchi, M., & Galli, A. (2012) · PPAR Research · doi:10.1155/2012/641087 · Cited by 245
Inoue, S., Unsinger, J., Davis, C. G., Muenzer, J. T., Ferguson, T. A., Chang, K., Osborne, D. F., Clark, A. T., Coopersmith, C. M., McDunn, J. E., et al. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0902307 · Cited by 229
Enhancing Nrf2 Pathway by Disruption of Keap1 in Myeloid Leukocytes Protects against Sepsis
Kong, X., Thimmulappa, R., Craciun, F., Harvey, C., Singh, A., Kombairaju, P., Reddy, S. P., Remick, D., & Biswal, S. (2011) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201102-0271oc · Cited by 222
Hodgin, K., & Moss, M. (2008) · Current Pharmaceutical Design · doi:10.2174/138161208784980590 · Cited by 215
DNA Damage and Repair: Relevance to Mechanisms of Neurodegeneration
Martin, L. J. (2008) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31816ff780 · Cited by 207
Antioxidant supplementation in sepsis and systemic inflammatory response syndrome
Berger, M. M., & Chioléro, R. L. (2007) · Critical Care Medicine · doi:10.1097/01.ccm.0000279189.81529.c4 · Cited by 206
EVALUATION OF ENDOTOXIN MODELS FOR THE STUDY OF SEPSIS
Remick, D. G., & Ward, P. A. (2005) · Shock · doi:10.1097/01.shk.0000191384.34066.85 · Cited by 202
Self-citationMacGarvey, N. C., Suliman, H. B., Bartz, R. R., Fu, P., Withers, C. M., Welty-Wolf, K. E., & Piantadosi, C. A. (2012) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201106-1152oc · Cited by 184
Acute Respiratory Distress Syndrome: Pathophysiology and Therapeutic Options
Pierrakos (2012) · Journal of Clinical Medicine Research · doi:10.4021/jocmr761w · Cited by 175
Sepsis Induces Early Alterations in Innate Immunity That Impact Mortality to Secondary Infection
Delano, M. J., Thayer, T., Gabrilovich, S., Kelly-Scumpia, K. M., Winfield, R. D., Scumpia, P. O., Cuenca, A. G., Warner, E., Wallet, S. M., Wallet, M. A., et al. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1002104 · Cited by 165
The Harmful Role of C5a on Innate Immunity in Sepsis
Ward, P. A. (2010) · Journal of Innate Immunity · doi:10.1159/000317194 · Cited by 159
Self-citationBench-to-bedside review: Sepsis - from the redox point of view
Andrades, M., Morina, A., Spasić, S., & Spasojević, I. (2011) · Critical Care · doi:10.1186/cc10334 · Cited by 158
Role of Endothelial Chemokines and Their Receptors during Inflammation
Speyer, C. L., & Ward, P. A. (2011) · Journal of Investigative Surgery · doi:10.3109/08941939.2010.521232 · Cited by 145
Self-citationStojanovich, L., Milovanovich, B., Luka, S. R. D., Popovich-Kuzmanovich, D., Bisenić, V., Djukanovich, B., Randjelovich, T., & Krotin, M. (2007) · Lupus · doi:10.1177/0961203306076223 · Cited by 143
Coopersmith, C. M., Wunsch, H., Fink, M. P., Linde‐Zwirble, W. T., Olsen, K. M., Sommers, M. S., Anand, K. J. S., Tchorz, K. M., Angus, D. C., & Deutschman, C. S. (2012) · Critical Care Medicine · doi:10.1097/ccm.0b013e31823c8d03 · Cited by 142
The Lingering Consequences of Sepsis: A Hidden Public Health Disaster?
Angus, D. C. (2010) · JAMA · doi:10.1001/jama.2010.1546 · Cited by 136
Cavassani, K. A., Carson, W. F., Serezani, A. P. M., Wen, H., Schaller, M. A., Ishii, M., Lindell, D. M., Dou, Y., Lukacs, N. W., Keshamouni, V. G., et al. (2010) · Blood · doi:10.1182/blood-2009-09-241083 · Cited by 133
Novel Insights for Systemic Inflammation in Sepsis and Hemorrhage
Cai, B., Deitch, E. A., & Ulloa, L. (2010) · Mediators of Inflammation · doi:10.1155/2010/642462 · Cited by 123
Mathews, M. T., & Berk, B. C. (2008) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.107.156406 · Cited by 120
Cannabinoids: A New Group of Agonists of PPARs
Sun, Y., & Bennett, A. (2007) · PPAR Research · doi:10.1155/2007/23513 · Cited by 115
In vivo profile of the human leukocyte microRNA response to endotoxemia
Schmidt, W. M., Spiel, A. O., Jilma, B., Wolzt, M., & Müller, M. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.12.190 · Cited by 113
CD11c+ Dendritic Cells Are Required for Survival in Murine Polymicrobial Sepsis
Scumpia, P. O., McAuliffe, P. F., O’Malley, K. A., Ungaro, R. F., Uchida, T., Matsumoto, T., Remick, D. G., Clare-Salzler, M. J., Moldawer, L. L., & Efron, P. A. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.5.3282 · Cited by 101
Anti‐inflammatory effects of β 2 adrenergic receptor agonists in experimental acute lung injury
Bosmann, M., Grailer, J. J., Zhu, K., Matthay, M. A., Sarma, J. V., Zetoune, F. S., & Ward, P. A. (2012) · The FASEB Journal · doi:10.1096/fj.11-201640 · Cited by 94
Self-citationMoore, S., & Mackenzie, A. B. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900394 · Cited by 87
Role of oxidative stress in experimental sepsis and multisystem organ dysfunction
Crimi, E., Sica, V., Slutsky, A. S., Zhang, H., Williams‐Ignarro, S., Ignarro, L. J., & Claudio Napoli, A. (2006) · Free Radical Research · doi:10.1080/10715760600669612 · Cited by 83
Standage, S. W., Caldwell, C. C., Zingarelli, B., & Wong, H. R. (2011) · Shock · doi:10.1097/shk.0b013e31823f1a00 · Cited by 82
Activation of Nrf2-Regulated Glutathione Pathway Genes by Ischemic Preconditioning
Bell, K. F. S., Fowler, J. H., Al-Mubarak, B. R., Horsburgh, K. J., & Hardingham, G. E. (2011) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2011/689524 · Cited by 82
Zanotti-Cavazzoni, S. L., & Goldfarb, R. D. (2009) · Critical Care Clinics · doi:10.1016/j.ccc.2009.08.005 · Cited by 81
Ward, P. A. (2011) · JAMA · doi:10.1001/jama.2011.1831 · Cited by 76
Self-citationNeutrophil-derived ROS contribute to oxidative DNA damage induction by quartz particles
van Berlo, D., Wessels, A., Boots, A. W., Wilhelmi, V., Scherbart, A. M., Gerloff, K., van Schooten, F., Albrecht, C., & Schins, R. P. F. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.08.031 · Cited by 64
Oxidative stress as a novel target in pediatric sepsis management
Bettina Von Dessauer, G., Bongain, J., Molina, V., Quilodrán, J., Castillo, R. L., & Rodrigo, R. (2010) · Journal of Critical Care · doi:10.1016/j.jcrc.2010.05.001 · Cited by 64
Bosmann, M., Haggadone, M. D., Hemmila, M. R., Zetoune, F. S., Sarma, J. V., & Ward, P. A. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1102914 · Cited by 56
Self-citationAnimal models of sepsis and its complications
Fink, M. P. (2008) · Kidney International · doi:10.1038/ki.2008.442 · Cited by 48
Silva, E., Passos, R. D. H., Ferri, M. B., & de Figueiredo, L. F. P. (2008) · Clinics · doi:10.1590/s1807-59322008000100019 · Cited by 43
The Cholinergic Anti-Inflammatory Pathway and the Gastrointestinal Tract
Bonaz, B. L. (2007) · Gastroenterology · doi:10.1053/j.gastro.2007.08.061 · Cited by 40
Activation of survival and apoptotic signaling pathways in lymphocytes exposed to palmitic acid
Takahashi, H., Cambiaghi, T. D., Luchessi, A. D., Hirabara, S. M., Vinolo, M. A. R., Newsholme, P., & Curi, R. (2011) · Journal of Cellular Physiology · doi:10.1002/jcp.22740 · Cited by 39
DIFFERENTIAL EXPRESSION OF TOLL-LIKE RECEPTOR GENES
Lissauer, M. E., Johnson, S. B., Bochicchio, G. V., Feild, C. J., Cross, A. S., Hasday, J. D., Whiteford, C. C., Nussbaumer, W. A., Towns, M., & Scalea, T. M. (2009) · Shock · doi:10.1097/shk.0b013e3181834991 · Cited by 39
Curcumin modulates leukocyte and platelet adhesion in murine sepsis.
Vachharajani, V., Wang, S., Mishra, N., El-Gazzar, M., Yoza, B. K., & McCall, C. E. (2010) · Microcirculation · doi:10.1111/j.1549-8719.2010.00039.x · Cited by 37
Barrera, G., Toaldo, C., Pizzimenti, S., Cerbone, A., Pettazzoni, P., Dianzani, M. U., & Ferretti, C. (2008) · PPAR Research · doi:10.1155/2008/524671 · Cited by 27
Novel Therapeutic Agents in Pediatric Sepsis: Peroxisome Proliferator Receptor γ (PPAR γ) Agonists
Kaplan, J. M., & Zingarelli, B. (2011) · The Open Inflammation Journal · doi:10.2174/1875041901104010120 · Cited by 11
Where have all the T cells gone?
Sereti, I. (2009) · Blood · doi:10.1182/blood-2009-04-217091 · Cited by 11
Khazaei, M., Salehi, E., & Rashidi, B. (2012) · International Journal of Peptides · doi:10.1155/2012/637212 · Cited by 11
Kamal, A. K. (2007) · Neurosciences · doi:10.17712/1658-3183.1489 · Cited by 10
Using Innate Immunity to Characterize the Host Response to Microbial Invasion in Severe Sepsis
Warner, E. A., & Moldawer, L. L. (2008) · Future Microbiology · doi:10.2217/17460913.3.2.177 · Cited by 6
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Metadata
- Authors
- Bosmann, M., & Ward, P. A.
- Venue
- Trends in Immunology
- Publisher
- Elsevier BV
- Published
- 2013-03
- Volume
- 34
- Issue
- 3
- Pages
- 129-136
- ISSN
- 1471-4906 (ISSN-L)
- OpenAlex
- W2080196545
- Cited by
- 558
- References
- 65
- FWCI
- 2.95
- Type
- journal article
- Language
- en
- Open access
- green
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