Source:http://linkedlifedata.com/resource/pubmed/id/21486386
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2011-6-7
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pubmed:abstractText |
Cytomegalovirus (CMV) infection is a common complication after organ transplantation. Previous studies have demonstrated that activating killer-cell immunoglobulin-like receptors (KIR) may reduce the rate of CMV infection. KIR genes can be divided into haplotype A (containing a fixed set of inhibitory receptors) and haplotype B (carrying additional activating KIR genes). The KIR locus is divided into a centromeric and a telomeric portion, both of which may carry A or B haplotype motifs. We studied a cohort of 339 kidney transplant recipients to elucidate which KIR genes protect from CMV infection. CMV infection occurred in 139 patients (41%). Possession of telomeric (hazard ratio 0.64, 95% confidence interval 0.44-0.94, p = 0.02) but not centromeric (HR 0.86, 95% CI 0.60-1.23, p = 0.41) B motifs was associated with statistically significant protection from CMV infection. Due to linkage disequilibrium, we were not able to identify a single protective gene within the telomeric B complex (which may contain the KIR2DS1, KIR3DS1, KIR2DL5A and KIR2DS5 genes). The presence of known or putative ligands to activating KIR did not significantly modify the influence of telomeric B group genes. We confirm that B haplotypes protect from CMV infection after kidney transplantation and show that this arises from telomeric B haplotype genes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1600-6143
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pubmed:author | |
pubmed:copyrightInfo |
©2011 The Authors Journal compilation©2011 The American Society of Transplantation and the American Society of Transplant Surgeons.
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pubmed:issnType |
Electronic
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1302-7
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pubmed:meshHeading |
pubmed-meshheading:21486386-Adolescent,
pubmed-meshheading:21486386-Adult,
pubmed-meshheading:21486386-Aged,
pubmed-meshheading:21486386-Aged, 80 and over,
pubmed-meshheading:21486386-Centromere,
pubmed-meshheading:21486386-Child,
pubmed-meshheading:21486386-Child, Preschool,
pubmed-meshheading:21486386-Cohort Studies,
pubmed-meshheading:21486386-Cytomegalovirus Infections,
pubmed-meshheading:21486386-Female,
pubmed-meshheading:21486386-Humans,
pubmed-meshheading:21486386-Kidney Transplantation,
pubmed-meshheading:21486386-Male,
pubmed-meshheading:21486386-Middle Aged,
pubmed-meshheading:21486386-Receptors, KIR,
pubmed-meshheading:21486386-Telomere,
pubmed-meshheading:21486386-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
Telomeric rather than centromeric activating KIR genes protect from cytomegalovirus infection after kidney transplantation.
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pubmed:affiliation |
Immunotherapy Laboratory, Department of Biomedicine, University Hospital, Basel, Switzerland. sternm@uhbs.ch
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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