Open AccessHeterogeneity of humoral immune abnormalities in children with Nijmegen breakage syndrome: an 8‐year follow‐up study in a single centre
Author(s) -
GREGOREK H.,
CHRZANOWSKA K. H.,
MICHAL´KIEWICZ J.,
SYCZEWSKA M.,
MADALIN´SKI K.
Publication year - 2002
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1046/j.1365-2249.2002.01971.x
Subject(s) - nijmegen breakage syndrome , immunology , immune system , medicine , biology , genetics , dna , dna damage , ataxia telangiectasia
Summary During an 8‐year period of observation, defects of immune responses were characterized and monitored in 40 of 50 Polish children with Nijmegen breakage syndrome referred to the Children's Memorial Health Institute in Warsaw. The following parameters were determined at diagnosis: (1) concentrations of serum IgM, IgG, IgA; (2) concentrations of IgG subclasses; and (3) lymphocyte subpopulations. In addition, naturally acquired specific antibodies against Streptococcus pneumoniae were determined in 20 patients with a history of recurrent respiratory infections. During follow‐up, total serum immunoglobulins and IgG subclasses were monitored systematically in 17 patients who did not receive immunomodulatory therapy. Moreover, anti‐HBs antibody response was measured after vaccination of 20 children against HBV. We found that the immune deficiency in NBS is profound, highly variable, with a tendency to progress over time. Systematic monitoring of the humoral response, despite good clinical condition, is essential for early medical intervention.