Source:http://linkedlifedata.com/resource/pubmed/id/10820292
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2000-6-21
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pubmed:abstractText |
The development of chronic graft-versus-host disease (GVHD), which is induced by the transfer of DBA/2 spleen cells into (C57BL/6 x DBA/2)F1 (BDF1) mice, is closely related to diminished donor anti-host CTL activity and host B cell hyperactivation. Therefore, an approach which activates donor CD8+ T cells or suppresses donor CD4+ T cell-host B cell interaction may have clinical utility in the treatment of chronic GVHD. We have previously demonstrated that IL-18 induces the development of naive CD8+ T cells into type I effector cells in DBA/2 anti-BDF1 MLC. In this paper we examined the effect of IL-18 administration on the development of chronic GVHD in mice. The treatment was started before or after the onset of clinical evidence of the disease. Regardless of the treatment schedule, IL-18 significantly decreased immunological parameters indicative of chronic GVHD, such as elevated serum IgG antinuclear Abs, IgG1, and IgE levels, and host B cell numbers and their activation. Importantly, IL-18-treated mice did not show the same acute GVHD-like symptoms reported for IL-12 treatment, because there was no weight loss, death, or severe immunodeficiency as indicated by a decrease in IL-2 and IFN-gamma production by Con A-stimulated spleen cells. In contrast, IL-18 treatment partially but significantly restored the production of these cytokines. Data further suggested that these IL-18-mediated therapeutic effects may be due to the induction of donor CD8+ CTL, the decrease in donor CD4+ T cell numbers, and a down-regulation of host B cell MHC class II expression. Thus, our results suggest that IL-18 has beneficial effects in the prevention and treatment of chronic GVHD.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
164
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6067-74
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:10820292-Acute Disease,
pubmed-meshheading:10820292-Animals,
pubmed-meshheading:10820292-B-Lymphocytes,
pubmed-meshheading:10820292-CD4-CD8 Ratio,
pubmed-meshheading:10820292-CD4-Positive T-Lymphocytes,
pubmed-meshheading:10820292-CD8-Positive T-Lymphocytes,
pubmed-meshheading:10820292-Chronic Disease,
pubmed-meshheading:10820292-Drug Administration Schedule,
pubmed-meshheading:10820292-Female,
pubmed-meshheading:10820292-Graft vs Host Disease,
pubmed-meshheading:10820292-Injections, Intraperitoneal,
pubmed-meshheading:10820292-Interleukin-18,
pubmed-meshheading:10820292-Lymphopenia,
pubmed-meshheading:10820292-Mice,
pubmed-meshheading:10820292-Mice, Inbred DBA,
pubmed-meshheading:10820292-T-Lymphocytes, Cytotoxic
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pubmed:year |
2000
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pubmed:articleTitle |
IL-18 prevents the development of chronic graft-versus-host disease in mice.
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pubmed:affiliation |
Fujisaki Institute, Hayashibara Biochemical Laboratories, Inc., Okayama, Japan. kohnok@hayashibara.co.jp
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pubmed:publicationType |
Journal Article
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