Source:http://linkedlifedata.com/resource/pubmed/id/17766682
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2007-11-16
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pubmed:abstractText |
Administration of high-dose intact human immunoglobulin (IH-Ig) has been applied to treat a variety of inflammatory and autoimmune diseases, and is expected to have beneficial effects on human fecundity. In the present study, we investigated whether Ig had anti-resorption effects using polyinosinic-polycytidylic acid sodium salt [poly (I:C)]-induced enhancement of fetal resorption in the mating of CBA/J x DBA/2J resorption-prone mouse model. Furthermore, we investigated the mechanism of the effect by examining the mRNA expression of interferon (IFN)-gamma, tumor necrosis factor (TNF)-alpha, IL-10, IL-4 and TGF-beta(1) in spleens and placentas from the resorption-prone model treated with IH-Ig, by reverse transcription (RT)-polymerase chain reaction (PCR). Administration of high-dose IH-Ig significantly reduced the fetal resorption rate from 55% to 10%. This anti-resorption effect, however, was not detected in mice administered with Fab fragments of human Ig. We then performed adoptive transfer experiments to examine whether cellular components could transfer the effect. A remarkable anti-resorption effect was seen in poly (I:C)-injected pregnant recipients transferred with spleen cells from IH-Ig-treated donor mice. The RT-PCR study showed that IH-Ig reduced the expression of IFN-gamma and TNF-alpha mRNA in placentas of poly (I:C)-injected pregnant mice. The present findings demonstrate that intact Ig, particularly its Fc portion, possesses anti-resorption activity. The effect might be attributed to the suppressed production of pro-inflammatory cytokines at the maternofetal interface.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Fluoresceins,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulins,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-10,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/carboxyfluoresceindiacetate
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1460-2407
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
807-14
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:17766682-Animals,
pubmed-meshheading:17766682-Female,
pubmed-meshheading:17766682-Fetal Resorption,
pubmed-meshheading:17766682-Flow Cytometry,
pubmed-meshheading:17766682-Fluoresceins,
pubmed-meshheading:17766682-Gene Expression,
pubmed-meshheading:17766682-Immunoglobulin G,
pubmed-meshheading:17766682-Immunoglobulins,
pubmed-meshheading:17766682-Interferon-gamma,
pubmed-meshheading:17766682-Interleukin-10,
pubmed-meshheading:17766682-Interleukin-4,
pubmed-meshheading:17766682-Male,
pubmed-meshheading:17766682-Mice,
pubmed-meshheading:17766682-Placenta,
pubmed-meshheading:17766682-Pregnancy,
pubmed-meshheading:17766682-RNA, Messenger,
pubmed-meshheading:17766682-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:17766682-Spleen,
pubmed-meshheading:17766682-Transforming Growth Factor beta,
pubmed-meshheading:17766682-Tumor Necrosis Factor-alpha
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pubmed:year |
2007
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pubmed:articleTitle |
Administration of high-dose intact immunoglobulin has an anti-resorption effect in a mouse model of reproductive failure.
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pubmed:affiliation |
Division of Immunobiology, Research Section of Pathophysiology, Institute for Genetic Medicine, Hokkaido University, Kita-15, Nishi-7, Kita-ku, Sapporo, Hokkaido, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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