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Background: Common variable immunodeficiency (CVID) and IgG deficiency are 2 of the more prevalent primary humoral immune defects. The former is defined by consensus with criteria for quantitative and qualitative antibody defects, whereas the latter is used to describe patients with reduced IgG, who commonly have recurrent sinopulmonary infections but do not fulfill CVID criteria. However, these patients are often given this diagnosis.
Objective: To compare immunologic findings and clinical manifestations of 2 large cohorts of patients with CVID or IgG deficiency to better delineate differences between these syndromes.
Methods: We extracted clinical and laboratory data from electronic medical records of patients at our institution who had received International Classification of Disease codes for either CVID, or IgG deficiency. We gathered immunoglobulin levels, lymphocyte subpopulation counts, and serological vaccine responses. In some patients, we performed flow cytometry to determine percentages of memory and switched-memory B cells. We compiled and statistically compared clinical data related to infectious manifestations, bronchiectasis, autoimmune diseases, infiltrative inflammatory processes, and lymphoid malignancies.
Results: In contrast to IgG-deficient patients, we found that patients with CVID had lower IgG levels, greater unresponsiveness to most vaccines, lower percentages of memory and isotype switched-memory B cells, and lower CD4 T-cell counts. Clinically, patients with CVID presented similar rates of sinusitis and pneumonias, but a significantly higher prevalence of bronchiectasis and especially noninfectious complications.
Conclusions: CVID and IgG deficiency do not share the same disease spectrum, the former being associated with immunodysregulative manifestations and markers of a more severe immune defect. These data may allow clinicians to distinguish these conditions and the management differences that these patients pose.
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http://dx.doi.org/10.1016/j.jaip.2018.12.004 | DOI Listing |
Oman Med J
March 2025
Freelance Public Health Senior Consultant, Muscat, Oman.
Objectives: Selective immunoglobulin A deficiency (SIgAD) is characterized by an isolated deficiency of serum IgA while immunoglobulin G (IgG) and immunoglobulin M (IgM) levels remain normal. Symptoms range from asymptomatic to recurrent infections. We aimed to determine the prevalence of IgAD and SIgAD among Omani patients undergoing screening for celiac disease.
View Article and Find Full Text PDFArthritis Rheumatol
July 2025
Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Objective: Interleukin-17-producing CD4 Th17 cells contribute to the pathogenesis of autoimmune diseases, including crescentic glomerulonephritis. Although ADAM9 has been reported to contribute to organ inflammation, the mechanism remains poorly understood. The goal of the current study was to investigate how ADAM9 alters T cell metabolism to promote the generation of Th17 cell differentiation.
View Article and Find Full Text PDFJ Ethnopharmacol
August 2025
Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210032, PR China; Jiangsu Province Hospital of Chinese Medicine, Nanjing, 210032, PR China; Nanjing University of Chinese Medicine, Nanjing, 210032, PR China. Electronic address:
Ethnopharmacological Relevance: Sjögren's syndrome (SS) is an autoimmune disorder primarily characterized by the involvement of exocrine glands. Currently, effective interventions need to be explored to preserve glandular function. Maidong Dishao Decoction (MDDST), which has been widely used in the treatment of Sjögren's syndrome for over 20 years, functions to nourish yin and promote fluid production, as well as to regulate lung qi to distribute body fluids-particularly benefiting patients with yin and fluid deficiency.
View Article and Find Full Text PDFClin Biochem
August 2025
Department of Central Diagnostic Laboratory, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands. Electronic address:
Background And Aims: Patients with primary antibody deficiencies receiving immunoglobulin replacement therapy require frequent monitoring of immunoglobulin G (IgG) levels. Capillary IgG measurements from dried blood spots (DBS) or microtubes offer several advantages over samples obtained by venipuncture, including facilitating remote self-sampling. However, the validity of this alternative method is still unknown.
View Article and Find Full Text PDFJ Am Soc Nephrol
August 2025
Graduate Institute of Aerospace and Undersea Medicine, National Defense Medical University, Taipei, Taiwan.
Background: IgA nephropathy is the most common form of glomerulonephritis and a leading cause of kidney failure. Ample evidence confirms the deposition of IgA and IgG, as well as the infiltration of mononuclear leukocytes in kidney biopsy specimens from IgA nephropathy patients. Previously, we established an experimental IgA nephropathy model in B cell-deficient mice, implicating interactions between Fcγ receptors (FcγRs) in the pathogenesis of IgA nephropathy.
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