The transcriptome of the fetal inflammatory response syndrome.
The transcriptome of the fetal inflammatory response syndrome.
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DOI:
10.1111/j.1600-0897.2009.00791.x
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发表时间:
2010-01
期刊:
影响因子:
--
通讯作者:
Draghici S
中科院分区:
文献类型:
--
作者:
Madsen-Bouterse SA;Romero R;Tarca AL;Kusanovic JP;Espinoza J;Kim CJ;Kim JS;Edwin SS;Gomez R;Draghici S
The fetal inflammatory response syndrome (FIRS) is considered the counterpart of the systemic inflammatory response syndrome (SIRS), but similarities in their regulatory mechanisms are unclear. This study characterizes the fetal mRNA transcriptome of peripheral leukocytes to identify key biological processes and pathways involved in FIRS. Umbilical cord blood from preterm neonates with FIRS (funisitis, plasma IL-6>11 pg/ml; n=10) and neonates with no evidence of inflammation (n=10) was collected at birth. Microarray analysis of leukocyte RNA revealed differential expression of 541 unique genes, changes confirmed by qRT-PCR for 41 or of 44 genes tested. Similar to SIRS and sepsis, ontological and pathway analyses yielded significant enrichment of biological processes including antigen processing and presentation, immune response, and processes critical to cellular metabolism. Results are comparable with microarray studies of endotoxin challenge models and pediatric sepsis, identifying 25 genes across all studies. This study is the first to profile genome-wide expression in FIRS, which demonstrates a substantial degree of similarity with SIRS despite differences in fetal and adult immune systems.
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影响因子:
3.6
作者:
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通讯作者:
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DOI:
10.1902/annals.2001.6.1.153
发表时间:
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期刊:
Annals of periodontology
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