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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
1996-11-27
pubmed:abstractText
Four pancreatic islet-specific CD4+ helper T (Th) 1 (Th1) clones and two Th1 clones transduced with an SRalpha promoter-linked murine IL-10 (mIL-10) cDNA of 2.0-6.0 x 10(6) cells were adoptively transferred to nonobese diabetic (NOD) mice at age 8 d. Cyclophosphamide (CY) was administered at age 37 d (plus CY), and the incidence of diabetes and the histological grade of insulitis were examined at age 47 d. After the adoptive transfer of IL-10-transduced Th1 cells, polymerase chain reaction (PCR) and reverse-transcription (RT)-PCR detected the neo gene and the retrovirus vector-mediated IL-10 mRNA in situ in recipient islets, respectively. RT-PCR detected the decrease of IFN-gamma mRNA relative to IL-10 mRNA in IL-10-transduced Th1 clones in vitro and also in recipient islets. All four wild type Th1 clones plus CY induced the insulitis grade of 2.75 and diabetes in 66% of recipient NOD mice. IL-10-transduced two Th1 clones plus CY induced periinsulitis with the grade of 1.43 and diabetes in 8.0%. The 1:1 mixture of wild type Th1 cells and IL-10-transduced Th1 cells plus CY induced periinsulitis with the grade of 1.85 and diabetes in 20%. The suppression of diabetes through decreasing IFN-gamma mRNA by the tissue-specific delivery of IL-10 to pancreatic islets with IL-10-transduced Th1 cells affords us the starting basis to develop the gene therapy for autoimmune diabetes.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-1422257, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-1628770, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-1899431, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-1902501, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-1909135, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2188676, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2194165, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2205920, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2307481, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2405400, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2449974, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2510155, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2523712, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2533502, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2661286, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2827008, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-2965652, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-3046964, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-3121415, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-3134263, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-3275717, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-3309126, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-3413107, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-3472348, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-3525284, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-3901813, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-6530055, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-7696210, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-7761837, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8064245, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8073945, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8100367, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8104408, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8132775, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8145050, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8181185, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8215637, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8315397, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8432410, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8476563, http://linkedlifedata.com/resource/pubmed/commentcorrection/8878437-8551245
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0021-9738
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
98
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1851-9
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1996
pubmed:articleTitle
Prevention of adoptively transferred diabetes in nonobese diabetic mice with IL-10-transduced islet-specific Th1 lymphocytes. A gene therapy model for autoimmune diabetes.
pubmed:affiliation
Otsuka Department of Clinical and Molecular Nutrition, School of Medicine, The University of Tokushima, Japan.
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