pubmed-article:7492751 | rdf:type | pubmed:Citation | lld:pubmed |
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pubmed-article:7492751 | lifeskim:mentions | umls-concept:C0208973 | lld:lifeskim |
pubmed-article:7492751 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:7492751 | pubmed:dateCreated | 1996-1-11 | lld:pubmed |
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pubmed-article:7492751 | pubmed:abstractText | The VH4-21 (V4-34) gene segment, a member of the VH4 family, is expressed early in B-cell maturation and is utilized by approximately 6% of normal adult B lymphocytes. This prevalence indicates an importance of VH4-21 in the B-cell repertoire. The gene also encodes certain autoantibodies being mandatory for pathological IgM anti-red cell antibodies directed against the I/i antigen, and also capable of encoding anti-DNA antibodies. Recognition of I/i antigen or DNA appears to be via two distinct sites on VH, with I/i binding mediated by sequences in the framework region, and DNA binding correlating with the presence of positively charged amino acids in complementarity-determining region 3. However, these positively charged residues appear to suppress the ability of the framework region to interact with I/i, rendering a single sequence monospecific for I/i or DNA. The IgM anti-DNA antibodies also recognize bacterial lipid A, whereas the anti-I/i antibodies do not, indicating that CDR3 may be involved in binding the negatively charged lipid A. Structural similarities between the DNA backbone and lipid A provide a possible explanation for this cross-reactivity. This dual recognition of bacterial antigen and autoantigen provides a potential link between infection and autoimmunity. | lld:pubmed |
pubmed-article:7492751 | pubmed:language | eng | lld:pubmed |
pubmed-article:7492751 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7492751 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:7492751 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7492751 | pubmed:issn | 0956-960X | lld:pubmed |
pubmed-article:7492751 | pubmed:author | pubmed-author:StevensonF... | lld:pubmed |
pubmed-article:7492751 | pubmed:author | pubmed-author:IsenbergD ADA | lld:pubmed |
pubmed-article:7492751 | pubmed:author | pubmed-author:ChapmanC JCJ | lld:pubmed |
pubmed-article:7492751 | pubmed:author | pubmed-author:SpellerbergM... | lld:pubmed |
pubmed-article:7492751 | pubmed:author | pubmed-author:MockridgeC... | lld:pubmed |
pubmed-article:7492751 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7492751 | pubmed:volume | 6 | lld:pubmed |
pubmed-article:7492751 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7492751 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7492751 | pubmed:pagination | 52-6 | lld:pubmed |
pubmed-article:7492751 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:7492751 | pubmed:year | 1995 | lld:pubmed |
pubmed-article:7492751 | pubmed:articleTitle | Dual recognition of lipid A and DNA by human antibodies encoded by the VH4-21 gene: a possible link between infection and lupus. | lld:pubmed |
pubmed-article:7492751 | pubmed:affiliation | Tenovus Laboratory, Southampton University Hospitals, UK. | lld:pubmed |
pubmed-article:7492751 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7492751 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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