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Escherichia coliO157 Fails to Induce a Long‐Lasting Lipopolysaccharide‐Specific, Measurable Humoral Immune Response in Children with Hemolytic‐Uremic Syndrome
Author(s) -
Kerstin U. Ludwig,
Martin Bitzan,
Christoph Bobrowski,
Dirk E. MüllerWiefel
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/341781
Subject(s) - immunology , antibody , escherichia coli , immune system , humoral immunity , immunoassay , lipopolysaccharide , antigen , immunoglobulin m , microbiology and biotechnology , immunoglobulin a , biology , immunity , immunoglobulin g , medicine , biochemistry , gene
Escherichia coli O157 lipopolysaccharide (LPS)-specific antibodies were measured in sequential serum samples from 131 children with serologically defined E. coli O157-associated hemolytic-uremic syndrome (HUS), using an enzyme immunoassay. On the basis of evaluation of 66 children with culture-proven E. coli O157 infection and serum samples from 132 age-matched control subjects, the assay showed a sensitivity of 95%, 88%, and 74% and a specificity of 99%, 99%, and 98% for IgM, IgA, and IgG, respectively. Anti-O157 LPS antibodies decreased below the cut-off levels in >50% of the children at 11 (IgM), 5 (IgA), and 11 weeks (IgG) after onset of diarrhea and 10, 4, and 10 weeks, respectively, after the onset of HUS. Children with enteropathic HUS fail to develop a long-lasting humoral immune response to the O157 antigen. Incomplete immunity to E. coli O157 may signal a risk for recurrent infections and has implications for serodiagnostic studies.

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