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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
Main Authors: RIJHSINGHANI, ASHA G., THOMPSON, KRISTIN, TYGRETTE, LORRAINE, BHATIA, SUDERSHAN K.
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container_title American journal of reproductive immunology (1989)
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creator RIJHSINGHANI, ASHA G.
THOMPSON, KRISTIN
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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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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. 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Psychology ; Gestation ; Growth rate ; Interleukin 10 ; Interleukin-10 - antagonists &amp; 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. 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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 &amp; 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. 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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. 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identifier ISSN: 1046-7408
ispartof American journal of reproductive immunology (1989), 1997-03, Vol.37 (3), p.232-235
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1600-0897
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source Wiley-Blackwell Read & Publish Collection
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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