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Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions

British Journal of Haematology · 2009 · Vol. 145(6) · pp. 709–727
Helen ChapelCharlotte Cunningham‐Rundles

Abstract

The common variable immunodeficiency disorders are a mixed group of heterogeneous conditions linked by lack of immunoglobulin production and primary antibody failure. This variability results in difficulty in making coherent sense of either immunopathogenesis or the role of various genetic abnormalities reported in the literature. The recent attempt to collate the varied complications in these conditions and to define particular clinical phenotypes has improved our understanding of these diseases. Once refined and confirmed by other studies, these definitions will facilitate improved accuracy of prognosis and better management of clinical complication. They may also provide a method of analysing outcomes as related to new immunopathological and genetic findings.

Immunodeficiency and Autoimmune DisordersPlatelet Disorders and TreatmentsBlood disorders and treatmentsCommon variable immunodeficiencyMedicineComplicationIntensive care medicinePrimary immunodeficiencyImmunologyAntibodyInternal medicineImmune system

MeSH terms

HumansImmunoglobulin GPolymorphism, GeneticSurvival RateImmunoglobulins, IntravenousCommon Variable ImmunodeficiencyAge of Onset

Funding

  • National Institutes of Health
  • National Institute of Allergy and Infectious Diseases
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Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions · Scinovex