Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2009-12-30
pubmed:abstractText
A small fraction of dietary protein survives enzymatic degradation and is absorbed in potentially antigenic form. This can trigger inflammatory responses in patients with celiac disease or food allergies, but typically induces systemic immunological tolerance (oral tolerance). At present it is not clear how dietary antigens are absorbed. Most food staples, including those with common antigens such as peanuts, eggs, and milk, contain long-chain triglycerides (LCT), which stimulate mesenteric lymph flux and postprandial transport of chylomicrons through mesenteric lymph nodes (MLN) and blood. Most dietary antigens, like ovalbumin (OVA), are emulsifiers, predicting affinity for chylomicrons. We hypothesized that chylomicron formation promotes intestinal absorption and systemic dissemination of dietary antigens.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-10391890, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-10766026, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-10779755, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-11181758, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-11276208, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-11340090, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-12069393, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-12538700, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-14633944, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-15170335, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-15891388, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-15995182, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-16208376, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-16310792, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-16386709, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-16533884, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-16894241, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-17332893, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-17484880, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-17560003, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-17569825, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-17620362, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-17673546, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-17951529, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-18815435, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-19158321, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-2380981, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-4335139, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-536559, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-7749826, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-7889419, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-8176234, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-8436400, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-8450032, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-8756486, http://linkedlifedata.com/resource/pubmed/commentcorrection/20041190-9918423
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1932-6203
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
e8442
pubmed:dateRevised
2011-10-24
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
Chylomicrons promote intestinal absorption and systemic dissemination of dietary antigen (ovalbumin) in mice.
pubmed:affiliation
Department of Internal Medicine, University of Kentucky, Lexington, Kentucky, United States of America.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural