1984
DOI: 10.1016/0090-1229(84)90001-1
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Lack of IgG in a healthy adult: A rare case of dysgammaglobulinemia with undetectable serum IgG, IgA2, and IgE

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Cited by 16 publications
(6 citation statements)
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“…This deficiency might be a new type of immunological disorder which manifests itself mainly during pregnancy and childbirth [6], since the mothers themselves did not suffer from an increased rate of infections. A recent report has indicated that even a total deficiency of IgG antibodies can be compensated by an increased production of IgM and the IgG-deficient individual can thereby avoid recur rent infections [ 12], corroborating this theory.…”
supporting
confidence: 59%
“…This deficiency might be a new type of immunological disorder which manifests itself mainly during pregnancy and childbirth [6], since the mothers themselves did not suffer from an increased rate of infections. A recent report has indicated that even a total deficiency of IgG antibodies can be compensated by an increased production of IgM and the IgG-deficient individual can thereby avoid recur rent infections [ 12], corroborating this theory.…”
supporting
confidence: 59%
“…In some cases, it also may occur as a consequence of abnormal T‐cell control or altered B‐cell function (6). Diminished T‐lymphocyte function directed to specific subclass induction or excessive T‐cell suppression may result in subclass deficiency (7).…”
Section: Discussionmentioning
confidence: 99%
“…Severe asthma may become associated with an increased susceptibility to infections if immunoglobulin or IgG subclass levels are suppressed as a result of various diseases or treatment‐associated conditions. Considering that many healthy individuals present with IgG subclass deficiencies (7,31), a direct relationship of these immunodeficiencies to infections should be considered with special care, especially with respect to the need for gamma globulin treatment. Some studies show an improvement of clinical conditions in patients with established immunodeficiencies upon treatment with gamma globulin (36).…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, T cells from SIgAD patients will support IgA production in vitro by B cells from normal subjects. In a few selected cases the defect is restricted to one of the two IgA subclasses and this is most often, although not invariably [ 26], due to deletions of the corresponding heavy chain constant region gene [ 27].…”
Section: Molecular Basismentioning
confidence: 99%