pubmed-article:8596934 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8596934 | lifeskim:mentions | umls-concept:C0021289 | lld:lifeskim |
pubmed-article:8596934 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:8596934 | lifeskim:mentions | umls-concept:C0020964 | lld:lifeskim |
pubmed-article:8596934 | lifeskim:mentions | umls-concept:C1423842 | lld:lifeskim |
pubmed-article:8596934 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
pubmed-article:8596934 | pubmed:issue | 5256 | lld:pubmed |
pubmed-article:8596934 | pubmed:dateCreated | 1996-4-17 | lld:pubmed |
pubmed-article:8596934 | pubmed:abstractText | The neonatal period has been thought of as a window in ontogeny, during which the developing immune system is particularly susceptible to tolerization. In the present study, the classic system for induction of neonatal tolerance to protein antigens was reexamined in mice. The presumably tolerogenic protocol was found to trigger a vigorous T helper cell type 2 (TH2) immune response. Thus, neonatal "tolerization" induces immune deviation, not tolerance in the immunological sense. Neonates are not immune privileged but generate TH2 or TH1 responses, depending on the mode of immunization. | lld:pubmed |
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pubmed-article:8596934 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8596934 | pubmed:language | eng | lld:pubmed |
pubmed-article:8596934 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8596934 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:8596934 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:8596934 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8596934 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8596934 | pubmed:month | Mar | lld:pubmed |
pubmed-article:8596934 | pubmed:issn | 0036-8075 | lld:pubmed |
pubmed-article:8596934 | pubmed:author | pubmed-author:TanG CGC | lld:pubmed |
pubmed-article:8596934 | pubmed:author | pubmed-author:ForsthuberTT | lld:pubmed |
pubmed-article:8596934 | pubmed:author | pubmed-author:LehmannP VPV | lld:pubmed |
pubmed-article:8596934 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8596934 | pubmed:day | 22 | lld:pubmed |
pubmed-article:8596934 | pubmed:volume | 271 | lld:pubmed |
pubmed-article:8596934 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8596934 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8596934 | pubmed:pagination | 1728-30 | lld:pubmed |
pubmed-article:8596934 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:8596934 | pubmed:year | 1996 | lld:pubmed |
pubmed-article:8596934 | pubmed:articleTitle | Induction of TH1 and TH2 immunity in neonatal mice. | lld:pubmed |
pubmed-article:8596934 | pubmed:affiliation | Department of Pathology, Case Western Reserve University, Cleveland, OH 44106-4943, USA. | lld:pubmed |
pubmed-article:8596934 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:8596934 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:8596934 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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