Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2009-7-17
pubmed:abstractText
Induction of peripheral tolerance by oral administration of low-dose beta-tubulin antigen may be an effective, antigen-specific method to suppress experimental autoimmune hearing loss. Five groups of mice were fed with phosphate-buffered saline (PBS), ovalbumin (OVA), 20, 30 or 200 microg of beta-tubulin, respectively. All mice were then immunized by beta-tubulin. Hearing thresholds were measured before and after immunization. Inner ear histology and cytokine profile were examined. Mice fed with 20 or 30 microg of beta-tubulin showed less hearing loss and less inner ear damage compared to the groups treated with PBS, OVA or 200 microg of beta-tubulin. Interferon-gamma (IFN-gamma) was decreased while interleukin-4 (IL-4), IL-5, IL-13 and TGF-beta were increased in both sera and in cell culture supernatants of the mice fed with 20 or 30 microg of beta-tubulin. However, no cytokine profile change was found in the group treated with 200 microg of tubulin. These results suggest that a low dose of beta-tubulin is active orally in an antigen-specific fashion and capable of inhibiting the autoimmune reactions in the inner ear by suppressing Th1 (IFN-gamma) and increasing Th2 and Th3 (IL-4, IL-5, IL-13 and TGF-beta) cytokines. Oral antigen tolerance may be used to treat autoimmune inner ear disease.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-10097125, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-10229871, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-10399007, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-11176215, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-11372925, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-11465824, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-11678165, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-11722636, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-11809732, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-12117539, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-12352677, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-12594253, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-12624500, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-1370356, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-15277028, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-16424176, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-1717550, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-1946445, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-3463976, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-3791692, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-7112122, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-7520605, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-7541826, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-7603570, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-7777346, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-8022835, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-8458379, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-8558017, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-8805632, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-9104744, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-9184699, http://linkedlifedata.com/resource/pubmed/commentcorrection/19365153-9834060
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1423-0275
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
71
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
135-41
pubmed:dateRevised
2010-9-27
pubmed:meshHeading
pubmed-meshheading:19365153-Administration, Oral, pubmed-meshheading:19365153-Animals, pubmed-meshheading:19365153-Autoimmune Diseases, pubmed-meshheading:19365153-Cells, Cultured, pubmed-meshheading:19365153-Cytokines, pubmed-meshheading:19365153-Disease Models, Animal, pubmed-meshheading:19365153-Dose-Response Relationship, Drug, pubmed-meshheading:19365153-Ear, Inner, pubmed-meshheading:19365153-Evoked Potentials, Auditory, Brain Stem, pubmed-meshheading:19365153-Female, pubmed-meshheading:19365153-Hearing Loss, pubmed-meshheading:19365153-Immune Tolerance, pubmed-meshheading:19365153-Immunization, pubmed-meshheading:19365153-Labyrinth Diseases, pubmed-meshheading:19365153-Lymphocytes, pubmed-meshheading:19365153-Mice, pubmed-meshheading:19365153-Mice, Inbred C57BL, pubmed-meshheading:19365153-Spleen, pubmed-meshheading:19365153-Tubulin
pubmed:year
2009
pubmed:articleTitle
Induction of tolerance by oral administration of beta-tubulin in an animal model of autoimmune inner ear disease.
pubmed:affiliation
Department of Medicine, Neuroscience Institute, University of Tennessee Health Science Center, Memphis, TN, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural