Failure of heavy chain glycosylation of IgG in some patients with common, variable agammaglobulinemia
- PMID: 1083397
- PMCID: PMC436792
- DOI: 10.1172/JCI108407
Failure of heavy chain glycosylation of IgG in some patients with common, variable agammaglobulinemia
Abstract
Four patients with common, variable agammaglobulinemia were preveiously reported to have normal numbers of circulating B lymphocytes which synthesized normal amounts of IgG in tissue culture but failed to secrete the newly synthesized IgG. The B lymphocytes of these patients fail to incorporate [3H]mannose and/or [3H]glucosamine into newly synthesized IgG, whereas such incorporation appears to occur just before IgG secretion in cultures of normal B lymphocytes.
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