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

被引:266
作者
Chapel, Helen [1 ,2 ]
Cunningham-Rundles, Charlotte [3 ]
机构
[1] Univ Oxford, Nuffield Dept Med, Dept Clin Immunol, Oxford, England
[2] Oxford Radcliffe Hosp, Oxford, England
[3] Mt Sinai Med Ctr, Dept Med, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
common variable immune deficiency disorders; antibody failure; clinical phenotypes; genetic findings; management of patients; PRIMARY ANTIBODY DEFICIENCIES; NODULAR REGENERATIVE HYPERPLASIA; CHRONIC LYMPHOCYTIC-LEUKEMIA; SELECTIVE IGA DEFICIENCY; HEPATITIS-C VIRUS; OF-THE-LITERATURE; MEMORY B-CELLS; PRIMARY HYPOGAMMAGLOBULINEMIA; INTRAVENOUS IMMUNOGLOBULIN; GRANULOMATOUS-DISEASE;
D O I
10.1111/j.1365-2141.2009.07669.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:709 / 727
页数:19
相关论文
共 125 条
[1]  
Aghamohammadi A, 2008, J INVEST ALLERG CLIN, V18, P266
[2]   Chronic urticaria and angioedema as the first presentations of common variable immunodeficiency [J].
Altschul, A ;
Cunningham-Rundles, C .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 110 (04) :664-665
[3]  
Antony FC, 2002, BRIT J DERMATOL, V147, P182
[4]   Vitamin D deficiency in the absence of enteropathy in three cases with common variable immunodeficiency [J].
Ardeniz, Omur ;
Avci, Cigir Biray ;
Sin, Aytul ;
Ozgen, Gokhan ;
Gunsar, Fulya ;
Mete, Nihal ;
Gulbahar, Okan ;
Kokuludag, Ali .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2008, 147 (01) :74-83
[5]   Common-variable immunodeficiency-related lymphomas associate with mutations and rearrangements of BCL-6:: Pathogenetic and histogenetic implications [J].
Ariatti, C ;
Vivenza, D ;
Capello, D ;
Migliazza, A ;
Parvis, G ;
Fassone, L ;
Buonaiuto, D ;
Savinelli, F ;
Rossi, D ;
Saglio, G ;
Gaidano, G .
HUMAN PATHOLOGY, 2000, 31 (07) :871-873
[6]   Granulomatous disease: Distinguishing primary antibody disease from sarcoidosis [J].
Arnold, D. F. ;
Wiggins, J. ;
Cunningham-Rundles, C. ;
Misbah, S. A. ;
Chapel, H. M. .
CLINICAL IMMUNOLOGY, 2008, 128 (01) :18-22
[7]   Vitamin E deficiency induced neurological disease in common variable immunodeficiency: two cases and a review of the literature of vitamin E deficiency [J].
Aslam, A ;
Misbah, SA ;
Talbot, K ;
Chapel, H .
CLINICAL IMMUNOLOGY, 2004, 112 (01) :24-29
[8]   Persistent activation of the tumor necrosis factor system in a subgroup of patients with common variable immunodeficiency-possible immunologic and clinical consequences [J].
Aukrust, P ;
Lien, E ;
Kristoffersen, AK ;
Muller, F ;
Haug, CJ ;
Espevik, T ;
Froland, SS .
BLOOD, 1996, 87 (02) :674-681
[9]  
Aukrust P, 2000, EUR J CLIN INVEST, V30, P252, DOI 10.1046/j.1365-2362.2000.00619.x
[10]   Granulomatous-lymphocytic lung disease shortens survival in common variable immunodeficiency [J].
Bates, CA ;
Ellison, MC ;
Lynch, DA ;
Cool, CD ;
Brown, KK ;
Routes, JM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2004, 114 (02) :415-421