Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1995-5-5
|
pubmed:abstractText |
Offspring of mother mice treated immediately after delivery with deaggregated human gamma-globulins (dHGG) are unable to produce HGG-specific antibodies when challenged with immunogenic forms of HGG (HGG/CFA) in adulthood. Despite a defective antibody response, animals rendered tolerant to HGG as neonates retain tolerogen-specific T cells able to proliferate and secrete lymphokines. The pattern of IL-2 and IL-4 secretion by T cells isolated from tolerant animals could not be distinguished from the corresponding cells in control mice, suggesting that neonatal exposure to dHGG did not affect T cell reactivity or Th1/Th2 in vivo balance. Moreover, immunization of tolerant animals with haptenated HGG confirmed the presence of tolerogen-specific helper T cells in vivo. Functional T cell depletion by anti-CD3 mAbs during lactation failed to modify induction of B cell tolerance, suggesting that T cells are neither affected nor required to induce the selective tolerance status observed in this model. Based on the finding that antigen-presenting cell functions in secondary organs (spleen, peritoneal cavity) are a late acquisition during ontogeny and reach adult-like levels at weaning, we propose that most soluble proteins elude T cell recognition during lactation due to defective antigen presentation.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/gamma-Globulins,
http://linkedlifedata.com/resource/pubmed/chemical/p-Azobenzenearsonate
|
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0008-8749
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
162
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
89-96
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:7535668-Animals,
pubmed-meshheading:7535668-Animals, Newborn,
pubmed-meshheading:7535668-Antibody Specificity,
pubmed-meshheading:7535668-Antigens,
pubmed-meshheading:7535668-B-Lymphocytes,
pubmed-meshheading:7535668-Cells, Cultured,
pubmed-meshheading:7535668-Female,
pubmed-meshheading:7535668-Humans,
pubmed-meshheading:7535668-Immune Tolerance,
pubmed-meshheading:7535668-Interleukin-2,
pubmed-meshheading:7535668-Interleukin-4,
pubmed-meshheading:7535668-Lactation,
pubmed-meshheading:7535668-Lymphocyte Activation,
pubmed-meshheading:7535668-Mice,
pubmed-meshheading:7535668-Mice, Inbred A,
pubmed-meshheading:7535668-T-Lymphocytes, Helper-Inducer,
pubmed-meshheading:7535668-gamma-Globulins,
pubmed-meshheading:7535668-p-Azobenzenearsonate
|
pubmed:year |
1995
|
pubmed:articleTitle |
Lack of T cell tolerance in mice exposed to a protein antigen through lactation.
|
pubmed:affiliation |
Laboratoire de Physiologie Animale, Université Libre de Bruxelles, Rhode-Saint-Genèse, Belgium.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|