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http://purl.uniprot.org/citations/22249367http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22249367http://www.w3.org/2000/01/rdf-schema#comment"

Background

Sialoadhesin (CD169) facilitates T-cell priming when overexpressed on inflammatory monocytes. Monocyte-derived macrophages prime acute cellular rejection after intestine transplantation (ITx).The purpose of this study was to evaluate whether CD169-expressing activated monocytes associate with or predict ITx rejection.

Methods

After informed consent (ClinicalTrials.gov NCT No. 01163578), activated CD169+CD14+monocytes were measured by flow cytometry in five normal healthy adult volunteers (group A), and 56 children with ITx sampled cross-sectionally (group B, 26), longitudinally (group C, 18), or during infection/inflammation without rejection (group D: acute enteritis, 9; Helicobacter pylori, 1; Streptococcal pharyngitis 1; and posttransplant lymphoma, 1). Activated monocytes were tested for correlations with donor-specific alloreactivity in simultaneous mixed lymphocyte co-cultures.

Results

Median age was 3 years (range 0.5-21 yr), and distribution of ITx-alone:combined liver-ITx was 25:31. Higher frequencies (%) of activated monocytes were seen during rejection in group B and infection/inflammation without rejection in group D (58 ± 28 and 73 ± 26), compared with nonrejectors or normal controls (10.6 ± 7.9 or 10.7 ± 6.5, P=0.001). In longitudinal monitoring, rejectors also showed higher activated monocyte frequencies (%) before ITx (64 ± 26 vs. 13.4 ± 8.6, P=0.0007) and during acute cellular rejection (55 ± 28 vs. 22.4 ± 15, P=0.006) when compared with nonrejectors. Activated monocytes correlated significantly with allospecific CD154+T-cytotoxic memory cells (Spearman r=0.688, P=7.1E-05) and CD154+B cells (r=0.518, P=0.005) in ITx recipients without inflammation/infection but not in group D.

Conclusions

Monocytes overexpress sialoadhesin nonspecifically during ITx rejection and systemic or enteritic inflammatory states. When combined with allospecific T and B cells, this information may differentiate between rejection and other enteritides."xsd:string
http://purl.uniprot.org/citations/22249367http://purl.org/dc/terms/identifier"doi:10.1097/tp.0b013e3182449189"xsd:string
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/author"Sun Q."xsd:string
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/author"Ashokkumar C."xsd:string
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/author"Ningappa M."xsd:string
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/author"Sindhi R."xsd:string
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/author"Mazariegos G."xsd:string
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/author"Gabriellan A."xsd:string
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/date"2012"xsd:gYear
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/name"Transplantation"xsd:string
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/pages"561-564"xsd:string
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/title"Increased monocyte expression of sialoadhesin during acute cellular rejection and other enteritides after intestine transplantation in children."xsd:string
http://purl.uniprot.org/citations/22249367http://purl.uniprot.org/core/volume"93"xsd:string
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http://purl.uniprot.org/citations/22249367http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/22249367
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