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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1990-7-27
pubmed:abstractText
To elucidate the abnormality of T cell differentiation in nude mice grafted with rat fetal thymus that develop multiple-organ-localized autoimmune diseases, we examined sequential appearance of T cell subsets and expression of TCR genes in BALB/c nude mice after grafting with fetal F344 rat thymus. We observed progressive expression of TCR gamma/delta-alpha/beta genes in the lymph node (LN) cells from 8 to 12 wk after grafting. An appreciable number of CD4+ T cells but few CD8+ T cells were detected in the LN at 8 wk after grafting. CD8+ T cells increased slowly in number by 12 wk after grafting but remained at a low level in comparison with those in nude mice 12 wk after grafting with BALB/c thymus. In correlation with an increase in the number of T cells expressing TCR alpha/beta genes, alloreactivity as assessed by MLR was increased to a normal level. However, CTL activity against alloantigens remained at a low level in the LN cells at 12 wk. At this stage, organ-specific autoimmune diseases and a high level of anti-DNA autoantibodies were detected. In these mice host-reactive T cells such as V beta 3- or V beta 11-bearing T cells were virtually eliminated in the peripheral mature T cell pool, whereas T cells maturing in the fetal rat thymus significantly proliferated in response to donor-rat stimulator cells. These results suggest that the development of the autoimmune diseases may be ascribed to an impaired maturation of CD8+ T cells but not to failure in clonal elimination of host-reactive T cells in nude mice grafted with rat thymus.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
145
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
28-35
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:2141617-Animals, pubmed-meshheading:2141617-Antibodies, Antinuclear, pubmed-meshheading:2141617-Antigens, Differentiation, T-Lymphocyte, pubmed-meshheading:2141617-Autoimmune Diseases, pubmed-meshheading:2141617-Blotting, Northern, pubmed-meshheading:2141617-Cell Differentiation, pubmed-meshheading:2141617-Flow Cytometry, pubmed-meshheading:2141617-Gene Expression, pubmed-meshheading:2141617-Immunity, Cellular, pubmed-meshheading:2141617-Lymph Nodes, pubmed-meshheading:2141617-Lymphocyte Culture Test, Mixed, pubmed-meshheading:2141617-Mice, pubmed-meshheading:2141617-Mice, Nude, pubmed-meshheading:2141617-RNA, Messenger, pubmed-meshheading:2141617-Rats, pubmed-meshheading:2141617-Receptors, Antigen, T-Cell, pubmed-meshheading:2141617-T-Lymphocytes, pubmed-meshheading:2141617-T-Lymphocytes, Cytotoxic, pubmed-meshheading:2141617-Thymus Gland
pubmed:year
1990
pubmed:articleTitle
Sequential appearance of host-derived T cell subsets during differentiation in nude mice grafted with rat fetal thymus.
pubmed:affiliation
Department of Immunology, School of Medicine, Kyushu University, Fukuoka, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't