HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Common variable immunodeficiency. Old questions are getting clearer.

Abstract
Common variable immunodeficiency (CVID) is a heterogeneous entity characterized by an impaired ability to produce antibodies. The failure is localized in partially mature B lymphocytes, though T lymphocyte abnormalities are occasionally present. This deficiency affects antibody synthesis and class switch from IgD and IgM, to IgG and IgA. CVID is related to selective IgA deficiency, and both abnormalities may coincide in one same family, and evolve from one to another in the same patient. The symptoms generally manifest in adults, but can occur at any age, even in infancy. Recurrent bacterial infections or pneumonias are frequent, and may be complicated by gastrointestinal problems, granulomas, autoimmune disorders or malignancies. A defect in memory B cells seems to condition the clinical severity. Recently, several mutations in genes encoding for molecules (CD19, TACI, ICOS) involved in B cell survival and isotype switch have been identified in patients with CVID. Nevertheless, genetic abnormalities have been found in less than 25 % of cases with CVID; the underlying mechanism thus remains unknown in the majority of CVID patients, and research in this field must continue.
AuthorsA Blanco-Quirós, P Solís-Sánchez, J A Garrote-Adrados, E Arranz-Sanz
JournalAllergologia et immunopathologia (Allergol Immunopathol (Madr)) 2006 Nov-Dec Vol. 34 Issue 6 Pg. 263-75 ISSN: 0301-0546 [Print] Singapore
PMID17173844 (Publication Type: Journal Article, Review)
Chemical References
  • B-Cell Activating Factor
  • Immunoglobulin G
  • Immunoglobulins
  • TNFRSF13B protein, human
  • TNFSF13B protein, human
  • Tnfsf13 protein, mouse
  • Tnfsf13b protein, mouse
  • Transmembrane Activator and CAML Interactor Protein
  • Tumor Necrosis Factor Ligand Superfamily Member 13
  • CD40 Ligand
  • Cimetidine
Topics
  • Adult
  • Aged
  • Animals
  • Antibody Formation
  • B-Cell Activating Factor (deficiency, immunology, physiology)
  • B-Lymphocytes (pathology)
  • CD40 Ligand (analysis)
  • Cell Differentiation
  • Child
  • Chronic Disease
  • Cimetidine (therapeutic use)
  • Common Variable Immunodeficiency (diagnosis, drug therapy, epidemiology, etiology, genetics, immunology)
  • Disease Models, Animal
  • Granuloma (etiology)
  • Humans
  • Immunoglobulin Class Switching
  • Immunoglobulin G (therapeutic use)
  • Immunoglobulins (biosynthesis)
  • Incidence
  • Infections (complications)
  • Lung Diseases (etiology)
  • Mice
  • Mice, Knockout
  • Middle Aged
  • Transmembrane Activator and CAML Interactor Protein (deficiency, immunology)
  • Tumor Necrosis Factor Ligand Superfamily Member 13 (deficiency, immunology, physiology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: