Source:http://linkedlifedata.com/resource/pubmed/id/11699204
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2001-11-8
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pubmed:abstractText |
B-cell chronic lymphocytic leukemia (B-CLL) is characterized by a malignant CD5+ B-cell clone. The leukemic clone commonly expresses IgM antibodies exhibiting reactivity toward a wide range of self-antigens. However, B-CLL associated autoimmunity is typically restricted to self-antigens expressed by blood cells, and mediated by IgG autoantibodies of polyclonal origin. In the present study, we addressed the question whether self-reactive antibody repertoires of plasma IgM and IgG are disturbed by monoclonal immunoglobulins of B-CLL patients, and whether antibody repertoires of patients exhibiting B-CLL associated target-restricted autoimmune disease (AID) differ from those of B-CLL patients without AID. We investigated antibody repertoires at a global level, using a technique of quantitative immunoblotting that allows for the quantitative screening of antibody reactivities in complex antibody mixtures toward a large panel of antigens derived from homologous tissue extracts, followed by multiparametric statistical analysis of the data. We demonstrate that self-reactive antibody repertoires of plasma IgM and IgG are broadly altered in patients with B-CLL, that alterations in self-reactive antibody repertoires are not restricted to B-CLL patients exhibiting AID, and that target-restricted autoimmunity in B-CLL patients is associated with altered antibody repertoires not restricted to the target organ. We conclude that monoclonal alterations of immunoglobulin production in B-CLL are associated with broad defects of self-reactive antibody repertoires. Our observations suggest that the application of therapeutic IVIg preparations might influence B-CLL by restoring normal self-reactive antibody repertoires in plasma.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1042-8194
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
163-76
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:11699204-Adult,
pubmed-meshheading:11699204-Aged,
pubmed-meshheading:11699204-Aged, 80 and over,
pubmed-meshheading:11699204-Autoantibodies,
pubmed-meshheading:11699204-Autoantigens,
pubmed-meshheading:11699204-Autoimmune Diseases,
pubmed-meshheading:11699204-Autoimmunity,
pubmed-meshheading:11699204-Case-Control Studies,
pubmed-meshheading:11699204-Female,
pubmed-meshheading:11699204-Humans,
pubmed-meshheading:11699204-Immunoblotting,
pubmed-meshheading:11699204-Immunoglobulin G,
pubmed-meshheading:11699204-Immunoglobulin M,
pubmed-meshheading:11699204-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:11699204-Male,
pubmed-meshheading:11699204-Middle Aged
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pubmed:year |
2001
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pubmed:articleTitle |
Broad alterations of self-reactive antibody-repertoires of plasma IgM and IgG in B-cell chronic lymphocytic leukemia (B-CLL) and B-CLL related target-restricted autoimmunity.
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pubmed:affiliation |
INSERM U430, Université Pierre et Marie Curie, Hôpital Broussais, Paris, France. stahld@uni-muenster.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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