Prevention of Lymphocyte Apoptosis—A Potential Treatment of Sepsis?
Sepsis is the leading cause of death in surgical intensive care units and is a major cause of morbidity and mortality in neonatal and medical intensive care units. The Centers for Disease Control and Prevention estimates that, in the United States alone, ∼500,000 people develop sepsis and 175,000 pe...
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Veröffentlicht in: | Clinical infectious diseases 2005-11, Vol.41 (Supplement-7), p.S465-S469 |
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description | Sepsis is the leading cause of death in surgical intensive care units and is a major cause of morbidity and mortality in neonatal and medical intensive care units. The Centers for Disease Control and Prevention estimates that, in the United States alone, ∼500,000 people develop sepsis and 175,000 people die each year. Sepsis is a growing problem; its incidence has tripled from 1972 to 1992. Recently, apoptosis has been identified as an important mechanism of cell death in animal models of sepsis and endotoxemia. During sepsis, there is extensive apoptotic death of lymphocytes and gastrointestinal epithelial cells. The extensive apoptotic death of lymphocytes is likely an important cause of the profound immunosuppression that is a hallmark of patients with sepsis. The apoptosis of gastrointestinal epithelial cells may compromise the integrity of the bowel wall, resulting in translocation of bacteria or endotoxins into the systemic circulation. The potential importance of apoptosis in the pathophysiology of sepsis is illustrated by results from animal models that demonstrate that blocking lymphocyte apoptosis improves survival in sepsis. A variety of strategies to inhibit apoptosis may ultimately provide an effective therapy for this highly lethal disorder. |
doi_str_mv | 10.1086/431998 |
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The Centers for Disease Control and Prevention estimates that, in the United States alone, ∼500,000 people develop sepsis and 175,000 people die each year. Sepsis is a growing problem; its incidence has tripled from 1972 to 1992. Recently, apoptosis has been identified as an important mechanism of cell death in animal models of sepsis and endotoxemia. During sepsis, there is extensive apoptotic death of lymphocytes and gastrointestinal epithelial cells. The extensive apoptotic death of lymphocytes is likely an important cause of the profound immunosuppression that is a hallmark of patients with sepsis. The apoptosis of gastrointestinal epithelial cells may compromise the integrity of the bowel wall, resulting in translocation of bacteria or endotoxins into the systemic circulation. The potential importance of apoptosis in the pathophysiology of sepsis is illustrated by results from animal models that demonstrate that blocking lymphocyte apoptosis improves survival in sepsis. A variety of strategies to inhibit apoptosis may ultimately provide an effective therapy for this highly lethal disorder.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1086/431998</identifier><identifier>PMID: 16237649</identifier><identifier>CODEN: CIDIEL</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>Animal models ; Animals ; Apoptosis ; B lymphocytes ; Bacterial diseases ; Bacterial sepsis ; Biological and medical sciences ; Caspase 8 - metabolism ; Caspase 9 - metabolism ; Caspase Inhibitors ; Cell death ; Death ; Endotoxemia - therapy ; Enzyme Inhibitors - therapeutic use ; Epithelial cells ; Human bacterial diseases ; Humans ; Immune system ; Infections ; Infectious diseases ; Ligands ; Lymphocyte receptors ; Lymphocytes ; Lymphocytes - immunology ; Lymphocytes - physiology ; Medical sciences ; Medical treatment ; Mitochondrial Membranes - metabolism ; Preventive medicine ; Receptors, Death Domain - metabolism ; Sepsis ; Sepsis - drug therapy ; Sepsis - epidemiology ; Sepsis - physiopathology ; Signal Transduction ; T lymphocytes ; United States - epidemiology</subject><ispartof>Clinical infectious diseases, 2005-11, Vol.41 (Supplement-7), p.S465-S469</ispartof><rights>Copyright 2005 The Infectious Diseases Society of America</rights><rights>2006 INIST-CNRS</rights><rights>Copyright University of Chicago, acting through its Press Nov 15, 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c522t-59458187d2a05d40fd38d724f2e2a2c4592c1c1b464fd8ff81775a98f5e7f7763</citedby><cites>FETCH-LOGICAL-c522t-59458187d2a05d40fd38d724f2e2a2c4592c1c1b464fd8ff81775a98f5e7f7763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4463590$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4463590$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,803,23930,23931,25140,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17331040$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16237649$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hotchkiss, Richard S.</creatorcontrib><creatorcontrib>Coopersmith, Craig M.</creatorcontrib><creatorcontrib>Karl, Irene E.</creatorcontrib><title>Prevention of Lymphocyte Apoptosis—A Potential Treatment of Sepsis?</title><title>Clinical infectious diseases</title><addtitle>Clinical Infectious Diseases</addtitle><description>Sepsis is the leading cause of death in surgical intensive care units and is a major cause of morbidity and mortality in neonatal and medical intensive care units. The Centers for Disease Control and Prevention estimates that, in the United States alone, ∼500,000 people develop sepsis and 175,000 people die each year. Sepsis is a growing problem; its incidence has tripled from 1972 to 1992. Recently, apoptosis has been identified as an important mechanism of cell death in animal models of sepsis and endotoxemia. During sepsis, there is extensive apoptotic death of lymphocytes and gastrointestinal epithelial cells. The extensive apoptotic death of lymphocytes is likely an important cause of the profound immunosuppression that is a hallmark of patients with sepsis. The apoptosis of gastrointestinal epithelial cells may compromise the integrity of the bowel wall, resulting in translocation of bacteria or endotoxins into the systemic circulation. The potential importance of apoptosis in the pathophysiology of sepsis is illustrated by results from animal models that demonstrate that blocking lymphocyte apoptosis improves survival in sepsis. A variety of strategies to inhibit apoptosis may ultimately provide an effective therapy for this highly lethal disorder.</description><subject>Animal models</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>B lymphocytes</subject><subject>Bacterial diseases</subject><subject>Bacterial sepsis</subject><subject>Biological and medical sciences</subject><subject>Caspase 8 - metabolism</subject><subject>Caspase 9 - metabolism</subject><subject>Caspase Inhibitors</subject><subject>Cell death</subject><subject>Death</subject><subject>Endotoxemia - therapy</subject><subject>Enzyme Inhibitors - therapeutic use</subject><subject>Epithelial cells</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Immune system</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Ligands</subject><subject>Lymphocyte receptors</subject><subject>Lymphocytes</subject><subject>Lymphocytes - immunology</subject><subject>Lymphocytes - physiology</subject><subject>Medical sciences</subject><subject>Medical treatment</subject><subject>Mitochondrial Membranes - metabolism</subject><subject>Preventive medicine</subject><subject>Receptors, Death Domain - metabolism</subject><subject>Sepsis</subject><subject>Sepsis - drug therapy</subject><subject>Sepsis - epidemiology</subject><subject>Sepsis - physiopathology</subject><subject>Signal Transduction</subject><subject>T lymphocytes</subject><subject>United States - epidemiology</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0N1qFDEUB_AgFret-gQig6B3U5NMPq_Kuqz9YNGiFaQ3IZtJcNaZyZhki3vnQ_QJ-yTNuEsXvPEqCf8f55wcAF4ieIKgYO9JhaQUT8AhohUvGZXoab5DKkoiKjEBRzGuIERIQPoMTBDDFWdEHoL5VbC3tk-N7wvvisWmG354s0m2mA5-SD428f7P3bS48mlUui2ug9Wpy4_Rf7VDFqfPwYHTbbQvducx-PZxfj07Lxefzy5m00VpKMappJJQgQSvsYa0JtDVlag5Jg5brLEhVGKDDFoSRlwtnBOIc6qlcNRyxzmrjsG7bd0h-F9rG5Pqmmhs2-re-nVUTHCIcov_wrwsisRf-OYfuPLr0OdPKDwiyXi1r2aCjzFYp4bQdDpsFIJqXL_arj_D17tq62Vn6z3b7TuDtzugo9GtC7o3Tdy73AxBArN7tXWrmHx4zAlhFZVjXG7jJib7-zHW4afK83Kqzr_fKHrz5dMl-yDzcA9YD6MB</recordid><startdate>20051115</startdate><enddate>20051115</enddate><creator>Hotchkiss, Richard S.</creator><creator>Coopersmith, Craig M.</creator><creator>Karl, Irene E.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T2</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7T5</scope><scope>7X8</scope></search><sort><creationdate>20051115</creationdate><title>Prevention of Lymphocyte Apoptosis—A Potential Treatment of Sepsis?</title><author>Hotchkiss, Richard S. ; Coopersmith, Craig M. ; Karl, Irene E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c522t-59458187d2a05d40fd38d724f2e2a2c4592c1c1b464fd8ff81775a98f5e7f7763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>B lymphocytes</topic><topic>Bacterial diseases</topic><topic>Bacterial sepsis</topic><topic>Biological and medical sciences</topic><topic>Caspase 8 - metabolism</topic><topic>Caspase 9 - metabolism</topic><topic>Caspase Inhibitors</topic><topic>Cell death</topic><topic>Death</topic><topic>Endotoxemia - therapy</topic><topic>Enzyme Inhibitors - therapeutic use</topic><topic>Epithelial cells</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Immune system</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Ligands</topic><topic>Lymphocyte receptors</topic><topic>Lymphocytes</topic><topic>Lymphocytes - immunology</topic><topic>Lymphocytes - physiology</topic><topic>Medical sciences</topic><topic>Medical treatment</topic><topic>Mitochondrial Membranes - metabolism</topic><topic>Preventive medicine</topic><topic>Receptors, Death Domain - metabolism</topic><topic>Sepsis</topic><topic>Sepsis - drug therapy</topic><topic>Sepsis - epidemiology</topic><topic>Sepsis - physiopathology</topic><topic>Signal Transduction</topic><topic>T lymphocytes</topic><topic>United States - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hotchkiss, Richard S.</creatorcontrib><creatorcontrib>Coopersmith, Craig M.</creatorcontrib><creatorcontrib>Karl, Irene E.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Immunology Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hotchkiss, Richard S.</au><au>Coopersmith, Craig M.</au><au>Karl, Irene E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevention of Lymphocyte Apoptosis—A Potential Treatment of Sepsis?</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clinical Infectious Diseases</addtitle><date>2005-11-15</date><risdate>2005</risdate><volume>41</volume><issue>Supplement-7</issue><spage>S465</spage><epage>S469</epage><pages>S465-S469</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>Sepsis is the leading cause of death in surgical intensive care units and is a major cause of morbidity and mortality in neonatal and medical intensive care units. The Centers for Disease Control and Prevention estimates that, in the United States alone, ∼500,000 people develop sepsis and 175,000 people die each year. Sepsis is a growing problem; its incidence has tripled from 1972 to 1992. Recently, apoptosis has been identified as an important mechanism of cell death in animal models of sepsis and endotoxemia. During sepsis, there is extensive apoptotic death of lymphocytes and gastrointestinal epithelial cells. The extensive apoptotic death of lymphocytes is likely an important cause of the profound immunosuppression that is a hallmark of patients with sepsis. The apoptosis of gastrointestinal epithelial cells may compromise the integrity of the bowel wall, resulting in translocation of bacteria or endotoxins into the systemic circulation. The potential importance of apoptosis in the pathophysiology of sepsis is illustrated by results from animal models that demonstrate that blocking lymphocyte apoptosis improves survival in sepsis. A variety of strategies to inhibit apoptosis may ultimately provide an effective therapy for this highly lethal disorder.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>16237649</pmid><doi>10.1086/431998</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animal models Animals Apoptosis B lymphocytes Bacterial diseases Bacterial sepsis Biological and medical sciences Caspase 8 - metabolism Caspase 9 - metabolism Caspase Inhibitors Cell death Death Endotoxemia - therapy Enzyme Inhibitors - therapeutic use Epithelial cells Human bacterial diseases Humans Immune system Infections Infectious diseases Ligands Lymphocyte receptors Lymphocytes Lymphocytes - immunology Lymphocytes - physiology Medical sciences Medical treatment Mitochondrial Membranes - metabolism Preventive medicine Receptors, Death Domain - metabolism Sepsis Sepsis - drug therapy Sepsis - epidemiology Sepsis - physiopathology Signal Transduction T lymphocytes United States - epidemiology |
title | Prevention of Lymphocyte Apoptosis—A Potential Treatment of Sepsis? |
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