Endotoxin-induced Chorioamnionitis Modulates Innate Immunity of Monocytes in Preterm Sheep
The preterm fetus is immune naive and has immature innate immune function. Although the preterm fetus is frequently exposed to chorioamnionitis, the effects of exposure of the fetal lung to inflammation on innate immune responses are unknown. Using the fetal sheep model of chorioamnionitis, cord blo...
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creator | Kramer, Boris W Ikegami, Machiko Moss, Timothy J. M Nitsos, Ilias Newnham, John P Jobe, Alan H |
description | The preterm fetus is immune naive and has immature innate immune function. Although the preterm fetus is frequently exposed to chorioamnionitis, the effects of exposure of the fetal lung to inflammation on innate immune responses are unknown. Using the fetal sheep model of chorioamnionitis, cord blood monocytes were isolated from preterm lambs 1 to 14 days after intra-amniotic endotoxin injection, cultured for approximately 16 hours, and challenged with endotoxin in vitro. Compared with monocytes from adult sheep, the preterm monocytes produced less H(2)O(2) and interleukin-6, and toll-like receptor 4 expression was decreased. Three days after intra-amniotic endotoxin exposure, preterm monocyte responses to in vitro endotoxin challenge demonstrated decreased H(2)O(2) and interleukin-6 production and decreased CD14 and major histocompatibility complex class II expression. Preterm monocyte responses 7 to 14 days after endotoxin tended to exceed those of adults and preterm control animals indicating augmented function. In contrast, a second intra-amniotic endotoxin injection 7 days after the initial endotoxin exposure suppressed monocyte function at 14 days. The fetal monocytes demonstrated patterns of responses consistent with endotoxin tolerance (immune paralysis) as well as maturation of function. Modulation of fetal innate immune responses by exposure to inflammation may alter subsequent immune adaptation after birth. |
doi_str_mv | 10.1164/rccm.200406-745OC |
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M ; Nitsos, Ilias ; Newnham, John P ; Jobe, Alan H</creator><creatorcontrib>Kramer, Boris W ; Ikegami, Machiko ; Moss, Timothy J. M ; Nitsos, Ilias ; Newnham, John P ; Jobe, Alan H</creatorcontrib><description>The preterm fetus is immune naive and has immature innate immune function. Although the preterm fetus is frequently exposed to chorioamnionitis, the effects of exposure of the fetal lung to inflammation on innate immune responses are unknown. Using the fetal sheep model of chorioamnionitis, cord blood monocytes were isolated from preterm lambs 1 to 14 days after intra-amniotic endotoxin injection, cultured for approximately 16 hours, and challenged with endotoxin in vitro. Compared with monocytes from adult sheep, the preterm monocytes produced less H(2)O(2) and interleukin-6, and toll-like receptor 4 expression was decreased. Three days after intra-amniotic endotoxin exposure, preterm monocyte responses to in vitro endotoxin challenge demonstrated decreased H(2)O(2) and interleukin-6 production and decreased CD14 and major histocompatibility complex class II expression. Preterm monocyte responses 7 to 14 days after endotoxin tended to exceed those of adults and preterm control animals indicating augmented function. In contrast, a second intra-amniotic endotoxin injection 7 days after the initial endotoxin exposure suppressed monocyte function at 14 days. The fetal monocytes demonstrated patterns of responses consistent with endotoxin tolerance (immune paralysis) as well as maturation of function. Modulation of fetal innate immune responses by exposure to inflammation may alter subsequent immune adaptation after birth.</description><identifier>ISSN: 1073-449X</identifier><identifier>ISSN: 0003-0805</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/rccm.200406-745OC</identifier><identifier>PMID: 15466254</identifier><language>eng</language><publisher>New York, NY: Am Thoracic Soc</publisher><subject>Amnion ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Antibodies ; Biological and medical sciences ; Blood coagulation. Blood cells ; Cells, Cultured ; Chorioamnionitis - chemically induced ; Chorioamnionitis - immunology ; Cytokines ; Drug toxicity and drugs side effects treatment ; E coli ; Endotoxins - administration & dosage ; Escherichia coli ; Female ; Fetal Blood - cytology ; Fetus - immunology ; Fetuses ; Fundamental and applied biological sciences. Psychology ; Histocompatibility Antigens Class II - analysis ; Hydrogen peroxide ; Hydrogen Peroxide - metabolism ; Immune Tolerance ; Immunity, Innate ; Inflammation ; Injections ; Intensive care medicine ; Interleukin-6 - biosynthesis ; Lipopolysaccharide Receptors - metabolism ; Medical sciences ; Membrane Glycoproteins - analysis ; Molecular and cellular biology ; Monocytes - immunology ; Nosocomial infections ; Phagocytosis ; Pharmacology. Drug treatments ; Platelet ; Pregnancy ; Receptors, Cell Surface - analysis ; Sheep ; Signal transduction ; Toll-Like Receptors ; Toxicity: blood</subject><ispartof>American journal of respiratory and critical care medicine, 2005-01, Vol.171 (1), p.73-77</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright American Thoracic Society Jan 1, 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-3748ae9436062acfd6b82053865904e6624ad7b5fac8a6cabade7b7c4a2d8a463</citedby><cites>FETCH-LOGICAL-c420t-3748ae9436062acfd6b82053865904e6624ad7b5fac8a6cabade7b7c4a2d8a463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,4011,4012,27900,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16437747$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15466254$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kramer, Boris W</creatorcontrib><creatorcontrib>Ikegami, Machiko</creatorcontrib><creatorcontrib>Moss, Timothy J. M</creatorcontrib><creatorcontrib>Nitsos, Ilias</creatorcontrib><creatorcontrib>Newnham, John P</creatorcontrib><creatorcontrib>Jobe, Alan H</creatorcontrib><title>Endotoxin-induced Chorioamnionitis Modulates Innate Immunity of Monocytes in Preterm Sheep</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><description>The preterm fetus is immune naive and has immature innate immune function. Although the preterm fetus is frequently exposed to chorioamnionitis, the effects of exposure of the fetal lung to inflammation on innate immune responses are unknown. Using the fetal sheep model of chorioamnionitis, cord blood monocytes were isolated from preterm lambs 1 to 14 days after intra-amniotic endotoxin injection, cultured for approximately 16 hours, and challenged with endotoxin in vitro. Compared with monocytes from adult sheep, the preterm monocytes produced less H(2)O(2) and interleukin-6, and toll-like receptor 4 expression was decreased. Three days after intra-amniotic endotoxin exposure, preterm monocyte responses to in vitro endotoxin challenge demonstrated decreased H(2)O(2) and interleukin-6 production and decreased CD14 and major histocompatibility complex class II expression. Preterm monocyte responses 7 to 14 days after endotoxin tended to exceed those of adults and preterm control animals indicating augmented function. In contrast, a second intra-amniotic endotoxin injection 7 days after the initial endotoxin exposure suppressed monocyte function at 14 days. The fetal monocytes demonstrated patterns of responses consistent with endotoxin tolerance (immune paralysis) as well as maturation of function. Modulation of fetal innate immune responses by exposure to inflammation may alter subsequent immune adaptation after birth.</description><subject>Amnion</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Biological and medical sciences</subject><subject>Blood coagulation. Blood cells</subject><subject>Cells, Cultured</subject><subject>Chorioamnionitis - chemically induced</subject><subject>Chorioamnionitis - immunology</subject><subject>Cytokines</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>E coli</subject><subject>Endotoxins - administration & dosage</subject><subject>Escherichia coli</subject><subject>Female</subject><subject>Fetal Blood - cytology</subject><subject>Fetus - immunology</subject><subject>Fetuses</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Histocompatibility Antigens Class II - analysis</subject><subject>Hydrogen peroxide</subject><subject>Hydrogen Peroxide - metabolism</subject><subject>Immune Tolerance</subject><subject>Immunity, Innate</subject><subject>Inflammation</subject><subject>Injections</subject><subject>Intensive care medicine</subject><subject>Interleukin-6 - biosynthesis</subject><subject>Lipopolysaccharide Receptors - metabolism</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins - analysis</subject><subject>Molecular and cellular biology</subject><subject>Monocytes - immunology</subject><subject>Nosocomial infections</subject><subject>Phagocytosis</subject><subject>Pharmacology. Drug treatments</subject><subject>Platelet</subject><subject>Pregnancy</subject><subject>Receptors, Cell Surface - analysis</subject><subject>Sheep</subject><subject>Signal transduction</subject><subject>Toll-Like Receptors</subject><subject>Toxicity: blood</subject><issn>1073-449X</issn><issn>0003-0805</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkNFqFDEUhoNYbK0-gDcyCIo3U5PJmWTmUpaqC5UWqiDehDNJxs0ySdZkBt23N-suFHp1Av93_hw-Ql4xesWYgA9Ja3_VUApU1BLa29UTcsFa3tbQS_q0vKnkNUD_45w8z3lLKWs6Rp-Rc9aCEE0LF-TndTBxjn9dqF0wi7amWm1ichF9cDG42eXqazTLhLPN1TqEMqu190uJ9lUcSxii3h9CF6q7ZGebfHW_sXb3gpyNOGX78jQvyfdP199WX-qb28_r1cebWkND55pL6ND2wAUVDerRiKFraMs70fYUbLkT0MihHVF3KDQOaKwcpAZsTIcg-CV5d-zdpfh7sXlW3mVtpwmDjUtWTHacCkkL-OYRuI1LCuU2xfpeNLLveIHYEdIp5pzsqHbJeUx7xag6WFcH6-poXf23XnZen4qXwVvzsHHSXIC3JwCzxmlMGLTLD5wALiXIwr0_chv3a_PHJauyx2kqtUzh9vAxk0wxJTn_BxzWmiw</recordid><startdate>20050101</startdate><enddate>20050101</enddate><creator>Kramer, Boris W</creator><creator>Ikegami, Machiko</creator><creator>Moss, Timothy J. 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Blood cells</topic><topic>Cells, Cultured</topic><topic>Chorioamnionitis - chemically induced</topic><topic>Chorioamnionitis - immunology</topic><topic>Cytokines</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>E coli</topic><topic>Endotoxins - administration & dosage</topic><topic>Escherichia coli</topic><topic>Female</topic><topic>Fetal Blood - cytology</topic><topic>Fetus - immunology</topic><topic>Fetuses</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Histocompatibility Antigens Class II - analysis</topic><topic>Hydrogen peroxide</topic><topic>Hydrogen Peroxide - metabolism</topic><topic>Immune Tolerance</topic><topic>Immunity, Innate</topic><topic>Inflammation</topic><topic>Injections</topic><topic>Intensive care medicine</topic><topic>Interleukin-6 - biosynthesis</topic><topic>Lipopolysaccharide Receptors - metabolism</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins - analysis</topic><topic>Molecular and cellular biology</topic><topic>Monocytes - immunology</topic><topic>Nosocomial infections</topic><topic>Phagocytosis</topic><topic>Pharmacology. Drug treatments</topic><topic>Platelet</topic><topic>Pregnancy</topic><topic>Receptors, Cell Surface - analysis</topic><topic>Sheep</topic><topic>Signal transduction</topic><topic>Toll-Like Receptors</topic><topic>Toxicity: blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kramer, Boris W</creatorcontrib><creatorcontrib>Ikegami, Machiko</creatorcontrib><creatorcontrib>Moss, Timothy J. 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M</au><au>Nitsos, Ilias</au><au>Newnham, John P</au><au>Jobe, Alan H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endotoxin-induced Chorioamnionitis Modulates Innate Immunity of Monocytes in Preterm Sheep</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>2005-01-01</date><risdate>2005</risdate><volume>171</volume><issue>1</issue><spage>73</spage><epage>77</epage><pages>73-77</pages><issn>1073-449X</issn><issn>0003-0805</issn><eissn>1535-4970</eissn><abstract>The preterm fetus is immune naive and has immature innate immune function. Although the preterm fetus is frequently exposed to chorioamnionitis, the effects of exposure of the fetal lung to inflammation on innate immune responses are unknown. Using the fetal sheep model of chorioamnionitis, cord blood monocytes were isolated from preterm lambs 1 to 14 days after intra-amniotic endotoxin injection, cultured for approximately 16 hours, and challenged with endotoxin in vitro. Compared with monocytes from adult sheep, the preterm monocytes produced less H(2)O(2) and interleukin-6, and toll-like receptor 4 expression was decreased. Three days after intra-amniotic endotoxin exposure, preterm monocyte responses to in vitro endotoxin challenge demonstrated decreased H(2)O(2) and interleukin-6 production and decreased CD14 and major histocompatibility complex class II expression. Preterm monocyte responses 7 to 14 days after endotoxin tended to exceed those of adults and preterm control animals indicating augmented function. In contrast, a second intra-amniotic endotoxin injection 7 days after the initial endotoxin exposure suppressed monocyte function at 14 days. The fetal monocytes demonstrated patterns of responses consistent with endotoxin tolerance (immune paralysis) as well as maturation of function. Modulation of fetal innate immune responses by exposure to inflammation may alter subsequent immune adaptation after birth.</abstract><cop>New York, NY</cop><pub>Am Thoracic Soc</pub><pmid>15466254</pmid><doi>10.1164/rccm.200406-745OC</doi><tpages>5</tpages></addata></record> |
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subjects | Amnion Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Antibodies Biological and medical sciences Blood coagulation. Blood cells Cells, Cultured Chorioamnionitis - chemically induced Chorioamnionitis - immunology Cytokines Drug toxicity and drugs side effects treatment E coli Endotoxins - administration & dosage Escherichia coli Female Fetal Blood - cytology Fetus - immunology Fetuses Fundamental and applied biological sciences. Psychology Histocompatibility Antigens Class II - analysis Hydrogen peroxide Hydrogen Peroxide - metabolism Immune Tolerance Immunity, Innate Inflammation Injections Intensive care medicine Interleukin-6 - biosynthesis Lipopolysaccharide Receptors - metabolism Medical sciences Membrane Glycoproteins - analysis Molecular and cellular biology Monocytes - immunology Nosocomial infections Phagocytosis Pharmacology. Drug treatments Platelet Pregnancy Receptors, Cell Surface - analysis Sheep Signal transduction Toll-Like Receptors Toxicity: blood |
title | Endotoxin-induced Chorioamnionitis Modulates Innate Immunity of Monocytes in Preterm Sheep |
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