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Inhibition of Interleukin-10 During Pregnancy Results in Neonatal Growth Retardation
PROBLEM: Interleukin 10 is considered to be important in the survival of the fetus in murine pregnancies that are known to be at risk for fetal wastage. The function of IL‐10 in a normal pregnancy is not known. METHODS: In this report, we attempted to neutralize Interleukin 10 by administering anti...
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Published in: | American journal of reproductive immunology (1989) 1997-03, Vol.37 (3), p.232-235 |
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container_title | American journal of reproductive immunology (1989) |
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creator | RIJHSINGHANI, ASHA G. THOMPSON, KRISTIN TYGRETTE, LORRAINE BHATIA, SUDERSHAN K. |
description | PROBLEM: Interleukin 10 is considered to be important in the survival of the fetus in murine pregnancies that are known to be at risk for fetal wastage. The function of IL‐10 in a normal pregnancy is not known.
METHODS: In this report, we attempted to neutralize Interleukin 10 by administering anti IL‐10 monoclonal antibodies (mAb) to pregnant mice that have a low background risk for fetal resorptions. The first group of mice was sacrificed on gestation day 18 to study the fetal effects of anti IL‐10 administration. The second group of mice was allowed to deliver to study the effects on the neonatal outcome.
RESULTS: Administration of anti IL‐10 mAb did not affect the duration of gestation or the fetal outcome. Neonates exposed to anti IL‐10 mAb in utero showed signs of transient growth deficiency starting at 4 weeks of age that spontaneously corrected by 6 weeks of age.
CONCLUSIONS: Administration of anti IL‐10 mAb does not alter the duration of gestation or the fetal outcome in normal murine pregnancies; however, it appears to be associated with transient neonatal growth problems. |
doi_str_mv | 10.1111/j.1600-0897.1997.tb00220.x |
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METHODS: In this report, we attempted to neutralize Interleukin 10 by administering anti IL‐10 monoclonal antibodies (mAb) to pregnant mice that have a low background risk for fetal resorptions. The first group of mice was sacrificed on gestation day 18 to study the fetal effects of anti IL‐10 administration. The second group of mice was allowed to deliver to study the effects on the neonatal outcome.
RESULTS: Administration of anti IL‐10 mAb did not affect the duration of gestation or the fetal outcome. Neonates exposed to anti IL‐10 mAb in utero showed signs of transient growth deficiency starting at 4 weeks of age that spontaneously corrected by 6 weeks of age.
CONCLUSIONS: Administration of anti IL‐10 mAb does not alter the duration of gestation or the fetal outcome in normal murine pregnancies; however, it appears to be associated with transient neonatal growth problems.</description><identifier>ISSN: 1046-7408</identifier><identifier>ISSN: 8755-8920</identifier><identifier>EISSN: 1600-0897</identifier><identifier>DOI: 10.1111/j.1600-0897.1997.tb00220.x</identifier><identifier>PMID: 9127644</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Age ; Animals ; Animals, Newborn ; Antibodies, Monoclonal - pharmacology ; Biological and medical sciences ; Birth Weight - drug effects ; Cell Differentiation - immunology ; Female ; Fetal Growth Retardation - etiology ; Fetal Growth Retardation - immunology ; Fetuses ; Fundamental and applied biological sciences. Psychology ; Gestation ; Growth rate ; Interleukin 10 ; Interleukin-10 - antagonists & inhibitors ; Interleukin-10 - immunology ; Male ; Mice ; Mice, Inbred BALB C ; Monoclonal antibodies ; Mother. Fetoplacental unit. Mammary gland. Milk ; neonatal growth ; Neonates ; Pregnancy ; Pregnancy Outcome ; Pregnancy. Parturition. Lactation ; Risk factors ; Survival ; T-Lymphocytes - cytology ; T-Lymphocytes - immunology ; Thymus Gland - immunology ; Vertebrates: reproduction</subject><ispartof>American journal of reproductive immunology (1989), 1997-03, Vol.37 (3), p.232-235</ispartof><rights>1997 Munksgaard</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4990-5e7cfb4ecdf5fa408f065f333b9a3031f42e1196348b73c2aecba453b43b22a23</citedby><cites>FETCH-LOGICAL-c4990-5e7cfb4ecdf5fa408f065f333b9a3031f42e1196348b73c2aecba453b43b22a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2644189$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9127644$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RIJHSINGHANI, ASHA G.</creatorcontrib><creatorcontrib>THOMPSON, KRISTIN</creatorcontrib><creatorcontrib>TYGRETTE, LORRAINE</creatorcontrib><creatorcontrib>BHATIA, SUDERSHAN K.</creatorcontrib><title>Inhibition of Interleukin-10 During Pregnancy Results in Neonatal Growth Retardation</title><title>American journal of reproductive immunology (1989)</title><addtitle>Am J Reprod Immunol</addtitle><description>PROBLEM: Interleukin 10 is considered to be important in the survival of the fetus in murine pregnancies that are known to be at risk for fetal wastage. The function of IL‐10 in a normal pregnancy is not known.
METHODS: In this report, we attempted to neutralize Interleukin 10 by administering anti IL‐10 monoclonal antibodies (mAb) to pregnant mice that have a low background risk for fetal resorptions. The first group of mice was sacrificed on gestation day 18 to study the fetal effects of anti IL‐10 administration. The second group of mice was allowed to deliver to study the effects on the neonatal outcome.
RESULTS: Administration of anti IL‐10 mAb did not affect the duration of gestation or the fetal outcome. Neonates exposed to anti IL‐10 mAb in utero showed signs of transient growth deficiency starting at 4 weeks of age that spontaneously corrected by 6 weeks of age.
CONCLUSIONS: Administration of anti IL‐10 mAb does not alter the duration of gestation or the fetal outcome in normal murine pregnancies; however, it appears to be associated with transient neonatal growth problems.</description><subject>Age</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Antibodies, Monoclonal - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Birth Weight - drug effects</subject><subject>Cell Differentiation - immunology</subject><subject>Female</subject><subject>Fetal Growth Retardation - etiology</subject><subject>Fetal Growth Retardation - immunology</subject><subject>Fetuses</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gestation</subject><subject>Growth rate</subject><subject>Interleukin 10</subject><subject>Interleukin-10 - antagonists & inhibitors</subject><subject>Interleukin-10 - immunology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Monoclonal antibodies</subject><subject>Mother. Fetoplacental unit. Mammary gland. Milk</subject><subject>neonatal growth</subject><subject>Neonates</subject><subject>Pregnancy</subject><subject>Pregnancy Outcome</subject><subject>Pregnancy. Parturition. Lactation</subject><subject>Risk factors</subject><subject>Survival</subject><subject>T-Lymphocytes - cytology</subject><subject>T-Lymphocytes - immunology</subject><subject>Thymus Gland - immunology</subject><subject>Vertebrates: reproduction</subject><issn>1046-7408</issn><issn>8755-8920</issn><issn>1600-0897</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqVkV1LHDEUhoO0qF39CYVBir2abb5msumFIH5sV0VFlF6GJJto1tmMJhnc_fdm2GEvC81Fcsj7nDeHNwAcIThGef1ajFENYQknnI0Rz1tSEGIMx6sdsL-VvuQa0rpkFE72wLcYFxDme8J2wS5HmNWU7oPHmX9xyiXX-qK1xcwnExrTvTpfIlicd8H55-I-mGcvvV4XDyZ2TYqF88Wtab1Msimmof1IL1lKMsxl73QAvlrZRHM4nCPwdHnxePanvLmbzs5Ob0pNOYdlZZi2iho9t5WVeUoL68oSQhSXBBJkKTYI8ZrQiWJEY2m0krQiihKFscRkBH5ufN9C-96ZmMTSRW2aRnrTdlHwHFaNOaWZPP4nmUPjjJNJBn9vQB3aGIOx4i24pQxrgaDowxeLHoaiT1j04YshfLHKzd-HVzq1NPNt65B21n8MuoxaNjbkTF3cYjgzKH_QCJxssA_XmPV_DCBOr2a5yAblxsDFZFZbAxleRc0Iq8Tf26moyBW95PRanJNPh92vdw</recordid><startdate>199703</startdate><enddate>199703</enddate><creator>RIJHSINGHANI, ASHA G.</creator><creator>THOMPSON, KRISTIN</creator><creator>TYGRETTE, LORRAINE</creator><creator>BHATIA, SUDERSHAN K.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</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>7T5</scope><scope>H94</scope></search><sort><creationdate>199703</creationdate><title>Inhibition of Interleukin-10 During Pregnancy Results in Neonatal Growth Retardation</title><author>RIJHSINGHANI, ASHA G. ; THOMPSON, KRISTIN ; TYGRETTE, LORRAINE ; BHATIA, SUDERSHAN K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4990-5e7cfb4ecdf5fa408f065f333b9a3031f42e1196348b73c2aecba453b43b22a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Age</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Antibodies, Monoclonal - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Birth Weight - drug effects</topic><topic>Cell Differentiation - immunology</topic><topic>Female</topic><topic>Fetal Growth Retardation - etiology</topic><topic>Fetal Growth Retardation - immunology</topic><topic>Fetuses</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gestation</topic><topic>Growth rate</topic><topic>Interleukin 10</topic><topic>Interleukin-10 - antagonists & inhibitors</topic><topic>Interleukin-10 - immunology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Monoclonal antibodies</topic><topic>Mother. Fetoplacental unit. Mammary gland. Milk</topic><topic>neonatal growth</topic><topic>Neonates</topic><topic>Pregnancy</topic><topic>Pregnancy Outcome</topic><topic>Pregnancy. Parturition. Lactation</topic><topic>Risk factors</topic><topic>Survival</topic><topic>T-Lymphocytes - cytology</topic><topic>T-Lymphocytes - immunology</topic><topic>Thymus Gland - immunology</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RIJHSINGHANI, ASHA G.</creatorcontrib><creatorcontrib>THOMPSON, KRISTIN</creatorcontrib><creatorcontrib>TYGRETTE, LORRAINE</creatorcontrib><creatorcontrib>BHATIA, SUDERSHAN K.</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>American journal of reproductive immunology (1989)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RIJHSINGHANI, ASHA G.</au><au>THOMPSON, KRISTIN</au><au>TYGRETTE, LORRAINE</au><au>BHATIA, SUDERSHAN K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of Interleukin-10 During Pregnancy Results in Neonatal Growth Retardation</atitle><jtitle>American journal of reproductive immunology (1989)</jtitle><addtitle>Am J Reprod Immunol</addtitle><date>1997-03</date><risdate>1997</risdate><volume>37</volume><issue>3</issue><spage>232</spage><epage>235</epage><pages>232-235</pages><issn>1046-7408</issn><issn>8755-8920</issn><eissn>1600-0897</eissn><abstract>PROBLEM: Interleukin 10 is considered to be important in the survival of the fetus in murine pregnancies that are known to be at risk for fetal wastage. The function of IL‐10 in a normal pregnancy is not known.
METHODS: In this report, we attempted to neutralize Interleukin 10 by administering anti IL‐10 monoclonal antibodies (mAb) to pregnant mice that have a low background risk for fetal resorptions. The first group of mice was sacrificed on gestation day 18 to study the fetal effects of anti IL‐10 administration. The second group of mice was allowed to deliver to study the effects on the neonatal outcome.
RESULTS: Administration of anti IL‐10 mAb did not affect the duration of gestation or the fetal outcome. Neonates exposed to anti IL‐10 mAb in utero showed signs of transient growth deficiency starting at 4 weeks of age that spontaneously corrected by 6 weeks of age.
CONCLUSIONS: Administration of anti IL‐10 mAb does not alter the duration of gestation or the fetal outcome in normal murine pregnancies; however, it appears to be associated with transient neonatal growth problems.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>9127644</pmid><doi>10.1111/j.1600-0897.1997.tb00220.x</doi><tpages>4</tpages></addata></record> |
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subjects | Age Animals Animals, Newborn Antibodies, Monoclonal - pharmacology Biological and medical sciences Birth Weight - drug effects Cell Differentiation - immunology Female Fetal Growth Retardation - etiology Fetal Growth Retardation - immunology Fetuses Fundamental and applied biological sciences. Psychology Gestation Growth rate Interleukin 10 Interleukin-10 - antagonists & inhibitors Interleukin-10 - immunology Male Mice Mice, Inbred BALB C Monoclonal antibodies Mother. Fetoplacental unit. Mammary gland. Milk neonatal growth Neonates Pregnancy Pregnancy Outcome Pregnancy. Parturition. Lactation Risk factors Survival T-Lymphocytes - cytology T-Lymphocytes - immunology Thymus Gland - immunology Vertebrates: reproduction |
title | Inhibition of Interleukin-10 During Pregnancy Results in Neonatal Growth Retardation |
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