Common variable immunodeficiency: a review

被引:67
作者
Di Renzo, M [1 ]
Pasqui, AL [1 ]
Auteri, A [1 ]
机构
[1] Univ Siena, Dept Clin Med & Immunol Sci, Div Internal Med, I-53100 Siena, Italy
关键词
common variable immunodeficiency; clinical symptoms; etiology; treatment; diagnosis;
D O I
10.1007/s10238-004-0027-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Common variable immunodeficiency (CVID) is the commonest symptomatic primary antibody deficiency syndrome. The predominant manifestation is hypogammaglobulinemia. CVID is characterized by recurrent bacterial infections, especially of the upper and lower respiratory airways, and is also associated with an increased incidence of autoimmune and neoplastic disorders. Most patients are diagnosed as adults and delay in the recognition of the disease is common. Several T and B cell defects have been described, although the underlying cause is still unknown.
引用
收藏
页码:211 / 217
页数:7
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共 70 条
  • [1] Absence of memory B cells in patients with common variable immunodeficiency
    Agematsu, K
    Futatani, T
    Hokibara, S
    Kobayashi, N
    Takamoto, M
    Tsukada, S
    Suzuki, H
    Koyasu, S
    Miyawaki, T
    Sugane, K
    Komiyama, A
    Ochs, HD
    [J]. CLINICAL IMMUNOLOGY, 2002, 103 (01) : 34 - 42
  • [2] Common-variable immunodeficiency-related lymphomas associate with mutations and rearrangements of BCL-6:: Pathogenetic and histogenetic implications
    Ariatti, C
    Vivenza, D
    Capello, D
    Migliazza, A
    Parvis, G
    Fassone, L
    Buonaiuto, D
    Savinelli, F
    Rossi, D
    Saglio, G
    Gaidano, G
    [J]. HUMAN PATHOLOGY, 2000, 31 (07) : 871 - 873
  • [3] Persistent activation of the tumor necrosis factor system in a subgroup of patients with common variable immunodeficiency-possible immunologic and clinical consequences
    Aukrust, P
    Lien, E
    Kristoffersen, AK
    Muller, F
    Haug, CJ
    Espevik, T
    Froland, SS
    [J]. BLOOD, 1996, 87 (02) : 674 - 681
  • [4] Elevated plasma levels of reduced homocysteine in common variable immunodeficiency - a marker of enhanced oxidative stress
    Aukrust, P
    Berge, RK
    Muller, F
    Ueland, PM
    Svardal, AM
    Froland, SS
    [J]. EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1997, 27 (09) : 723 - 730
  • [5] Primary immunodeficiency disorders: Antibody deficiency
    Ballow, M
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 109 (04) : 581 - 591
  • [6] Long-term outcome of chronic hepatitis C virus infection in primary hypogammaglobulinaemia
    Bjoro, K
    Skaug, K
    Haaland, T
    Froland, SS
    [J]. QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 1999, 92 (08) : 433 - 441
  • [7] Mycoplasma felis septic arthritis in a patient with hypogammaglobulinemia
    Bonilla, HF
    Chenoweth, CE
    Tully, JG
    Blythe, LK
    Robertson, JA
    Ognenovski, VM
    Kauffman, CA
    [J]. CLINICAL INFECTIOUS DISEASES, 1997, 24 (02) : 222 - 225
  • [8] Up-regulation of IL-12 in monocytes: A fundamental defect in common variable immunodeficiency
    Cambronero, R
    Sewell, WAC
    North, ME
    Webster, ADB
    Farrant, J
    [J]. JOURNAL OF IMMUNOLOGY, 2000, 164 (01) : 488 - 494
  • [9] Common variable immunodeficiency: Clinical and immunological features of 248 patients
    Cunningham-Rundles, C
    Bodian, C
    [J]. CLINICAL IMMUNOLOGY, 1999, 92 (01) : 34 - 48
  • [10] Hematologic complications of primary immune deficiencies
    Cunningham-Rundles, C
    [J]. BLOOD REVIEWS, 2002, 16 (01) : 61 - 64