Source:http://linkedlifedata.com/resource/pubmed/id/11007765
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2000-11-3
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pubmed:abstractText |
Brown-Norway (BN) rats are highly susceptible to drug-induced immune dysregulations and when injected with mercuric chloride (HgCl(2)) or sodium aurothiopropanolsulfonate (ATPS), they develop a syndrome characterized by a polyclonal B cell activation depending upon CD4(+) T(h)2 cells that recognize self-MHC class II molecules. Since peripheral tolerance of T(h)2 cells might be crucial in the prevention of immunological manifestations such as allergy, establishing conditions for inducing tolerance to HgCl(2)- or ATPS-mediated immune manifestations appeared to be of large interest. We report here that BN rats neonatally injected with HgCl(2): (i) do not develop the mercury disease, (ii) remain resistant to HgCl(2)-induced autoimmunity at 8 weeks of age and later, provided they are regularly exposed to HgCl(2), (iii) are still susceptible to ATPS-induced immune manifestations, and (iv) exhibit spleen cells that adoptively transfer tolerance to HgCl(2)-induced autoimmunity in naive, slightly irradiated, syngeneic recipients. These findings demonstrate that dominant specific tolerance can be neonatally induced using a chemical otherwise responsible for T(h)2-mediated autoimmunity.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Dimercaprol,
http://linkedlifedata.com/resource/pubmed/chemical/Mercuric Chloride,
http://linkedlifedata.com/resource/pubmed/chemical/Organogold Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Organometallic Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Propanols,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfhydryl Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/aurotioprol
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0953-8178
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1467-77
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:11007765-Adoptive Transfer,
pubmed-meshheading:11007765-Animals,
pubmed-meshheading:11007765-Animals, Newborn,
pubmed-meshheading:11007765-Autoimmunity,
pubmed-meshheading:11007765-CD8-Positive T-Lymphocytes,
pubmed-meshheading:11007765-Dimercaprol,
pubmed-meshheading:11007765-Immune Tolerance,
pubmed-meshheading:11007765-Mercuric Chloride,
pubmed-meshheading:11007765-Organogold Compounds,
pubmed-meshheading:11007765-Organometallic Compounds,
pubmed-meshheading:11007765-Propanols,
pubmed-meshheading:11007765-Rats,
pubmed-meshheading:11007765-Rats, Inbred BN,
pubmed-meshheading:11007765-Sulfhydryl Compounds,
pubmed-meshheading:11007765-Th2 Cells
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pubmed:year |
2000
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pubmed:articleTitle |
Neonatal induction of tolerance to T(h)2-mediated autoimmunity in rats.
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pubmed:affiliation |
INSERM U430 Hôpital Broussais, Pavillon Leriche, 96 rue Didot, 75674 Paris Cedex 14, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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