Placental cytokine and chemokine profiles reflect pregnancy outcomes in women exposed to Plasmodium falciparum infection
Pregnancy-associated malaria (PAM) can lead to severe complications for both mother and baby. Certain placental cytokine/chemokine profiles have been shown to reflect poor pregnancy outcomes, including maternal anemia and low birth weight. In intervillous plasma samples from 400 Beninese women livin...
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Veröffentlicht in: | Infection and immunity 2014-09, Vol.82 (9), p.3783-3789 |
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creator | Chêne, Arnaud Briand, Valérie Ibitokou, Samad Dechavanne, Sébastien Massougbodji, Achille Deloron, Philippe Luty, Adrian J F Gamain, Benoît Fievet, Nadine |
description | Pregnancy-associated malaria (PAM) can lead to severe complications for both mother and baby. Certain placental cytokine/chemokine profiles have been shown to reflect poor pregnancy outcomes, including maternal anemia and low birth weight. In intervillous plasma samples from 400 Beninese women living in an area where Plasmodium falciparum is endemic, we quantified 16 cytokines/chemokines. We assessed their profiles in groups with PAM, with maternal anemia, with preterm births, or with a low birth weight for gestational age. Repeated ultrasound measurements ensured that prematurity and low birth weight were highly accurate. Preliminary analyses revealed trends for lower cytokine/chemokine concentrations in placental plasma associated both with babies with low birth weight for gestational age and with P. falciparum infection during pregnancy, while, as a function of the latter, the concentration of gamma interferon (IFN-γ)-inducible protein 10 (IP-10) was higher. Multivariate analyses showed that (i) higher placental plasma interleukin-10 (IL-10) levels were associated with P. falciparum infections and (ii) independently of P. falciparum infections, lower concentrations of both IFN-γ and IL-5 were associated with low birth weight for gestational age. Our data further strengthen the idea that IL-10 and IP-10 could be useful diagnostic markers of P. falciparum infection during pregnancy. The concentrations of cytokines/chemokines in placental plasma may represent previously unrecognized markers of poor fetal growth. |
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Certain placental cytokine/chemokine profiles have been shown to reflect poor pregnancy outcomes, including maternal anemia and low birth weight. In intervillous plasma samples from 400 Beninese women living in an area where Plasmodium falciparum is endemic, we quantified 16 cytokines/chemokines. We assessed their profiles in groups with PAM, with maternal anemia, with preterm births, or with a low birth weight for gestational age. Repeated ultrasound measurements ensured that prematurity and low birth weight were highly accurate. Preliminary analyses revealed trends for lower cytokine/chemokine concentrations in placental plasma associated both with babies with low birth weight for gestational age and with P. falciparum infection during pregnancy, while, as a function of the latter, the concentration of gamma interferon (IFN-γ)-inducible protein 10 (IP-10) was higher. Multivariate analyses showed that (i) higher placental plasma interleukin-10 (IL-10) levels were associated with P. falciparum infections and (ii) independently of P. falciparum infections, lower concentrations of both IFN-γ and IL-5 were associated with low birth weight for gestational age. Our data further strengthen the idea that IL-10 and IP-10 could be useful diagnostic markers of P. falciparum infection during pregnancy. The concentrations of cytokines/chemokines in placental plasma may represent previously unrecognized markers of poor fetal growth.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/IAI.01922-14</identifier><identifier>PMID: 24958713</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Adult ; Chemokines - blood ; Cytokines - blood ; Female ; Fetal Blood - immunology ; Host Response and Inflammation ; Humans ; Interferon-gamma - blood ; Interferon-gamma - immunology ; Interleukin-10 - blood ; Interleukin-10 - immunology ; Interleukin-5 ; Malaria, Falciparum - blood ; Malaria, Falciparum - immunology ; Malaria, Falciparum - microbiology ; Placenta - immunology ; Placenta - microbiology ; Plasmodium falciparum ; Plasmodium falciparum - immunology ; Pregnancy ; Pregnancy Complications, Parasitic - blood ; Pregnancy Complications, Parasitic - immunology ; Pregnancy Complications, Parasitic - microbiology ; Pregnancy Outcome</subject><ispartof>Infection and immunity, 2014-09, Vol.82 (9), p.3783-3789</ispartof><rights>Copyright © 2014, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2014, American Society for Microbiology. All Rights Reserved. 2014 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-8ecf309b167f03352aff9f02c0fc3e35f305ae851a2ac5e8016dcaae75b1e51a3</citedby><cites>FETCH-LOGICAL-c483t-8ecf309b167f03352aff9f02c0fc3e35f305ae851a2ac5e8016dcaae75b1e51a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4187805/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4187805/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24958713$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chêne, Arnaud</creatorcontrib><creatorcontrib>Briand, Valérie</creatorcontrib><creatorcontrib>Ibitokou, Samad</creatorcontrib><creatorcontrib>Dechavanne, Sébastien</creatorcontrib><creatorcontrib>Massougbodji, Achille</creatorcontrib><creatorcontrib>Deloron, Philippe</creatorcontrib><creatorcontrib>Luty, Adrian J F</creatorcontrib><creatorcontrib>Gamain, Benoît</creatorcontrib><creatorcontrib>Fievet, Nadine</creatorcontrib><title>Placental cytokine and chemokine profiles reflect pregnancy outcomes in women exposed to Plasmodium falciparum infection</title><title>Infection and immunity</title><addtitle>Infect Immun</addtitle><description>Pregnancy-associated malaria (PAM) can lead to severe complications for both mother and baby. Certain placental cytokine/chemokine profiles have been shown to reflect poor pregnancy outcomes, including maternal anemia and low birth weight. In intervillous plasma samples from 400 Beninese women living in an area where Plasmodium falciparum is endemic, we quantified 16 cytokines/chemokines. We assessed their profiles in groups with PAM, with maternal anemia, with preterm births, or with a low birth weight for gestational age. Repeated ultrasound measurements ensured that prematurity and low birth weight were highly accurate. Preliminary analyses revealed trends for lower cytokine/chemokine concentrations in placental plasma associated both with babies with low birth weight for gestational age and with P. falciparum infection during pregnancy, while, as a function of the latter, the concentration of gamma interferon (IFN-γ)-inducible protein 10 (IP-10) was higher. Multivariate analyses showed that (i) higher placental plasma interleukin-10 (IL-10) levels were associated with P. falciparum infections and (ii) independently of P. falciparum infections, lower concentrations of both IFN-γ and IL-5 were associated with low birth weight for gestational age. Our data further strengthen the idea that IL-10 and IP-10 could be useful diagnostic markers of P. falciparum infection during pregnancy. The concentrations of cytokines/chemokines in placental plasma may represent previously unrecognized markers of poor fetal growth.</description><subject>Adult</subject><subject>Chemokines - blood</subject><subject>Cytokines - blood</subject><subject>Female</subject><subject>Fetal Blood - immunology</subject><subject>Host Response and Inflammation</subject><subject>Humans</subject><subject>Interferon-gamma - blood</subject><subject>Interferon-gamma - immunology</subject><subject>Interleukin-10 - blood</subject><subject>Interleukin-10 - immunology</subject><subject>Interleukin-5</subject><subject>Malaria, Falciparum - blood</subject><subject>Malaria, Falciparum - immunology</subject><subject>Malaria, Falciparum - microbiology</subject><subject>Placenta - immunology</subject><subject>Placenta - microbiology</subject><subject>Plasmodium falciparum</subject><subject>Plasmodium falciparum - immunology</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Parasitic - blood</subject><subject>Pregnancy Complications, Parasitic - immunology</subject><subject>Pregnancy Complications, Parasitic - microbiology</subject><subject>Pregnancy Outcome</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUU1P3DAQtaqismx76xn52EMD_kycC9IKFVhpJTjQs-V1xuA2sUOctOy_x8vCCm6cZua9p6eZeQh9p-SEUqZOl4vlCaE1YwUVn9CMkloVUjL2Gc1IxotaltUhOkrpTx6FEOoLOmSilqqifIYeb1pjIYymxXYzxr8-ADahwfYeut3UD9H5FhIewLVgxwzAXTDBbnCcRhu7TPmA_-cmYHjsY4IGjxFn49TFxk8ddqa1vjdDbn1w2cPH8BUdZDjBt5c6R78vft2eXxWr68vl-WJVWKH4WCiwjpN6TcvKEc4lM87VjjBLnOXAZSalASWpYcZKUISWjTUGKrmmkFE-R2c7335ad9Bsbx1Mq_vBd2bY6Gi8fs8Ef6_v4j8tqKoUkdngx4vBEB8mSKPufLLQtiZAnJKmsiyVkIrUH5BKzllObSv9uZPaIaaUX7vfiBK9zVXnXPVzrpqKLD9-e8Ve_BokfwIqLqHe</recordid><startdate>20140901</startdate><enddate>20140901</enddate><creator>Chêne, Arnaud</creator><creator>Briand, Valérie</creator><creator>Ibitokou, Samad</creator><creator>Dechavanne, Sébastien</creator><creator>Massougbodji, Achille</creator><creator>Deloron, Philippe</creator><creator>Luty, Adrian J F</creator><creator>Gamain, Benoît</creator><creator>Fievet, Nadine</creator><general>American Society for Microbiology</general><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>7X8</scope><scope>7T5</scope><scope>C1K</scope><scope>F1W</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>M7N</scope><scope>5PM</scope></search><sort><creationdate>20140901</creationdate><title>Placental cytokine and chemokine profiles reflect pregnancy outcomes in women exposed to Plasmodium falciparum infection</title><author>Chêne, Arnaud ; 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Certain placental cytokine/chemokine profiles have been shown to reflect poor pregnancy outcomes, including maternal anemia and low birth weight. In intervillous plasma samples from 400 Beninese women living in an area where Plasmodium falciparum is endemic, we quantified 16 cytokines/chemokines. We assessed their profiles in groups with PAM, with maternal anemia, with preterm births, or with a low birth weight for gestational age. Repeated ultrasound measurements ensured that prematurity and low birth weight were highly accurate. Preliminary analyses revealed trends for lower cytokine/chemokine concentrations in placental plasma associated both with babies with low birth weight for gestational age and with P. falciparum infection during pregnancy, while, as a function of the latter, the concentration of gamma interferon (IFN-γ)-inducible protein 10 (IP-10) was higher. Multivariate analyses showed that (i) higher placental plasma interleukin-10 (IL-10) levels were associated with P. falciparum infections and (ii) independently of P. falciparum infections, lower concentrations of both IFN-γ and IL-5 were associated with low birth weight for gestational age. Our data further strengthen the idea that IL-10 and IP-10 could be useful diagnostic markers of P. falciparum infection during pregnancy. The concentrations of cytokines/chemokines in placental plasma may represent previously unrecognized markers of poor fetal growth.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>24958713</pmid><doi>10.1128/IAI.01922-14</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Chemokines - blood Cytokines - blood Female Fetal Blood - immunology Host Response and Inflammation Humans Interferon-gamma - blood Interferon-gamma - immunology Interleukin-10 - blood Interleukin-10 - immunology Interleukin-5 Malaria, Falciparum - blood Malaria, Falciparum - immunology Malaria, Falciparum - microbiology Placenta - immunology Placenta - microbiology Plasmodium falciparum Plasmodium falciparum - immunology Pregnancy Pregnancy Complications, Parasitic - blood Pregnancy Complications, Parasitic - immunology Pregnancy Complications, Parasitic - microbiology Pregnancy Outcome |
title | Placental cytokine and chemokine profiles reflect pregnancy outcomes in women exposed to Plasmodium falciparum infection |
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