Literature DB >> 1988761

Common variable immunodeficiency: the disorder and treatment.

M W Yocum1, J M Kelso.   

Abstract

A case of common variable immunodeficiency, a relatively rare disorder, is presented. This case was complicated by the presence of an anti-IgA antibody in the patient's serum and a history of a possible anaphylactic reaction to a prior intravenous infusion of gamma-globulin. Common variable immunodeficiency is actually a heterogeneous group of demonstrable immunoglobulin deficiencies that have in common low levels of most immunoglobulin isotypes, the inability to form antibodies to antigen, an absence of gross defects in cell-mediated immunity, and the presence of recurrent bacterial infections. The history of immunoglobulin deficiency and its treatment is reviewed. Although the primary therapy for common variable immunodeficiency is gamma-globulin replacement, ancillary measures such as early treatment of infections with antibiotics are also important. Intravenous gamma-globulin replacement therapy is preferred to intramuscular replacement therapy in these patients because intramuscular doses must be limited in volume to minimize local pain and take 2 to 14 days to achieve maximal blood levels, during which time in situ degradation of up to 50% of the administered dose can occur. Five intravenous gamma-globulin preparations are currently available in the United States. The potential adverse effects of intravenous gamma-globulin infusion and the precautions currently taken to ensure safety during administration of this product are discussed.

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Year:  1991        PMID: 1988761     DOI: 10.1016/s0025-6196(12)61176-8

Source DB:  PubMed          Journal:  Mayo Clin Proc        ISSN: 0025-6196            Impact factor:   7.616


  5 in total

1.  Identification of a subset of common variable immunodeficiency patients with impaired B-cell protein tyrosine phosphorylation.

Authors:  R Schwartz; Y B Porat; Z Handzel; Z Sthoeger; B Z Garty; R Confino-Cohen; J Levy; I Zan-Bar
Journal:  Clin Diagn Lab Immunol       Date:  1999-11

2.  IgG anti-IgA subclasses in common variable immunodeficiency and association with severe adverse reactions to intravenous immunoglobulin therapy.

Authors:  R de Albuquerque Campos; M N Sato; A J da Silva Duarte
Journal:  J Clin Immunol       Date:  2000-01       Impact factor: 8.317

3.  Association of secondary amyloidosis with common variable immune deficiency and tuberculosis.

Authors:  Aykut Ferhat Celik; Mehmet Riza Altiparmak; Gülsüm Emel Pamuk; Omer Nuri Pamuk; Fehmi Tabak
Journal:  Yonsei Med J       Date:  2005-12-31       Impact factor: 2.759

4.  Reduced interleukin-2 (IL-2) production in common variable immunodeficiency is due to a primary abnormality of CD4+ T cell differentiation.

Authors:  E M Eisenstein; J S Jaffe; W Strober
Journal:  J Clin Immunol       Date:  1993-07       Impact factor: 8.317

5.  Secondary renal amyloidosis in a patient of pulmonary tuberculosis and common variable immunodeficiency.

Authors:  Manish R Balwani; Vivek B Kute; Pankaj R Shah; Pawan Wakhare; Hargovind L Trivedi
Journal:  J Nephropharmacol       Date:  2015-06-21
  5 in total

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