INT3512
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
IgA secretory piece and HBs antigen were not found in the glomeruli and early complement components C1q and C4 were absent. | |||||||||||||||
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Levels of serum IgG, IgA, and IgM fell significantly during treatment with SP, but none of the other changes reached statistical significance. | |||||||||||||||
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The pathogenic mechanisms underlying HSP are poorly understood, and whilst they may include gut infection, other mucosal mechanisms such as drugs or hypersensitivity have been postulated to lead to abnormalities in IgA synthesis [12]. | |||||||||||||||
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IgM was not significantly changed after glucocorticoid treatment in the patients with AIP, while IgG, IgG4 and IgA decreased. | |||||||||||||||
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Patients exposed to asbestos, and particularly those with asbestosis, have an increased incidence of ANA and other autoantibodies, and raised levels of IgG and IgA. | |||||||||||||||
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IgA ACAs were present in high titers in all groups and had little discriminant value in predicting thrombotic risk. | |||||||||||||||
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METHODS: We examined the immune condition of AIP patients before and after glucocorticoid treatment, focusing on serum levels of IgG, IgG4, IgM and IgA, and compared the results with those in other hepato-pancreatic diseases, such as autoimmune hepatitis, primary biliary cirrhosis, chronic pancreatitis and pancreatic carcinoma. | |||||||||||||||
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For phenotypic confirmation, mice were left unimmunized and verification of transferred IgMa -expressing B cells within the splenic FO B cell compartment of C57BL/6-Ighb recipient mice 1 d after transfer was validated by flow cytometry.
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For phenotypic confirmation, mice were left unimmunized and verification of transferred IgMa -expressing B cells within the splenic FO B cell compartment of C57BL/6-Ighb recipient mice 1 d after transfer was validated by flow cytometry.
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Selective immunoglobulin A deficiency (IgAD) is a primary immunodeficiency disease characterized by low levels (< 7 mg/dl) of serum immunoglobulin (Ig) A and normal serum levels of IgG and IgM. | |||||||||||||||
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