Common variable immune deficiency and autoimmunity

Autoimmunity Reviews

Volumn 5, Issue 7, 2006, Pages 465-470

  Brandt, Daniel ^a   Gershwin, M Eric ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Autoimmunity; Class switched memory B cells; Common variable immunodeficiency; Cytopenia; Granulomatous disease

Indexed keywords

CD20 ANTIBODY; CORTICOSTEROID; DANAZOL; ETANERCEPT; HYBRID PROTEIN; IMMUNOGLOBULIN; IMMUNOGLOBULIN G1; IMMUNOSUPPRESSIVE AGENT; INFLIXIMAB; RITUXIMAB; STEROID; TUMOR NECROSIS FACTOR ALPHA ANTIBODY; TUMOR NECROSIS FACTOR ALPHA RECEPTOR IMMUNOGLOBULIN G 1 FUSION PROTEIN; UNCLASSIFIED DRUG;

ANTIBODY PRODUCTION; AUTOIMMUNE DISEASE; AUTOIMMUNITY; COMMON VARIABLE IMMUNODEFICIENCY; CYTOPENIA; DRUG EFFECT; DRUG MEGADOSE; DRUG RESPONSE; ENTERITIS; GASTROINTESTINAL PAIN; GASTROINTESTINAL SYMPTOM; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GRAFT VERSUS HOST REACTION; GRANULOMA; HUMAN; HYPOGAMMAGLOBULINEMIA; IMMUNE DYSREGULATION; IMMUNOSUPPRESSIVE TREATMENT; INFLAMMATORY DISEASE; LYMPHOCYTOPENIA; NEUTROPENIA; NONHUMAN; REVIEW; SARCOIDOSIS; SPLENECTOMY;

ANIMALS; AUTOIMMUNITY; COMMON VARIABLE IMMUNODEFICIENCY; HUMANS;

EID: 33747273724     PISSN: 15689972     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.autrev.2006.03.010     Document Type: Review

References (37)

1. Cunningham-Rundles C., and Bodian C. Common variable immunodeficiency: clinical and immunological features of 248 patients. Clin Immunol 92 (1999) 34-48
2. Conley M.E., Park C.L., and Douglas S.D. Childhood common variable immunodeficiency with autoimmune disease. J Pediatr 108 (1986) 915-922
3. Wang J., and Cunningham-Rundles C. Treatment and outcome of autoimmune hematologic disease in common variable immunodeficiency (CVID). J Autoimmun 25 (2005) 57-62
4. Gershwin M.E., Blaese R.M., Steinberg A.D., Wistar Jr. R., and Strober W. Antibodies to nucleic acids in congenital immune deficiency states. J Pediatr 89 (1976) 377-381
5. Michel M., Chanet V., Galicier L., Ruivard M., Levy Y., Hermine O., et al. Autoimmune thrombocytopenic purpura and common variable immunodeficiency: analysis of 21 cases and review of the literature. Medicine (Baltimore) 83 (2004) 254-263
6. Cunningham-Rundles C. Hematologic complications of primary immune deficiencies. Blood Rev 16 (2002) 61-64
7. Hermaszewski R.A., and Webster A.D. Primary hypogammaglobulinaemia: a survey of clinical manifestations and complications. Q J Med 86 (1993) 31-42
8. Hausser C., Virelizier J.L., Buriot D., and Griscelli C. Common variable hypogammaglobulinemia in children. Clinical and immunologic observations in 30 patients. Am J Dis Child 137 (1983) 833-837
9. Tsokos G.C., Smith P.L., and Balow J.E. Development of hypogammaglobulinemia in a patient with systemic lupus erythematosus. Am J Med 81 (1986) 1081-1084
10. Fasano M.B., Sullivan K.E., Sarpong S.B., Wood R.A., Jones S.M., Johns C.J., et al. Sarcoidosis and common variable immunodeficiency. Report of 8 cases and review of the literature. Medicine (Baltimore) 75 (1996) 251-261
11. Mechanic L.J., Dikman S., and Cunningham-Rundles C. Granulomatous disease in common variable immunodeficiency. Ann Intern Med 127 (1997) 613-617
12. Hermans P.E., Diaz-Buxo J.A., and Stobo J.D. Idiopathic late-onset immunoglobulin deficiency. Clinical observations in 50 patients. Am J Med 61 (1976) 221-237
13. Andres E., Limbach F.X., Kurtz J.E., Kurtz-Illig V., Schaeverbeke T., Pflumio F., et al. Primary humoral immunodeficiency (late-onset common variable immunodeficiency) with antinuclear antibodies and selective immunoglobulin deficiency. Am J Med 111 (2001) 489-491
14. Baum C.G., Chiorazzi N., Frankel S., and Shepherd G.M. Conversion of systemic lupus erythematosus to common variable hypogammaglobulinemia. Am J Med 87 (1989) 449-456
15. Pordeus V., Litwin A., Levy Y., and Zandman-Goddard G. Hypogammaglobulinemia 31 years after the diagnosis of systemic lupus erythematosus. Isr Med Assoc J 6 (2004) 784
16. Stein A., Winkelstein A., and Agarwal A. Concurrent systemic lupus erythematosus and common variable hypogammaglobulinemia. Arthritis Rheum 28 (1985) 462-465
17. Sussman G.L., Rivera V.J., and Kohler P.F. Transition from systemic lupus erythematosus to common variable hypogammaglobulinemia. Ann Intern Med 99 (1983) 32-35
18. Swaak A.J., and van den Brink H.G. Common variable immunodeficiency in a patient with systemic lupus erythematosus. Lupus 5 (1996) 242-246
19. Agematsu K., Futatani T., Hokibara S., Kobayashi N., Takamoto M., Tsukada S., et al. Absence of memory B cells in patients with common variable immunodeficiency. Clin Immunol 103 (2002) 34-42
20. Aukrust P., Lien E., Kristoffersen A.K., Muller F., Haug C.J., Espevik T., et al. Persistent activation of the tumor necrosis factor system in a subgroup of patients with common variable immunodeficiency-possible immunologic and clinical consequences. Blood 87 (1996) 674-681
21. Kokron C.M., Errante P.R., Barros M.T., Baracho G.V., Camargo M.M., Kalil J., et al. Clinical and laboratory aspects of common variable immunodeficiency. An Acad Bras Cienc 76 (2004) 707-726
22. Sneller M.C., Strober W., Eisenstein E., Jaffe J.S., and Cunningham-Rundles C. NIH conference. New insights into common variable immunodeficiency. Ann Intern Med 118 (1993) 720-730
23. Spickett G.P., and Farrant J. The role of lymphokines in common variable hypogammaglobulinemia. Immunol Today 10 (1989) 192-194
24. Warnatz K., Wehr C., Drager R., Schmidt S., Eibel H., Schlesier M., et al. Expansion of CD19(hi)CD21(lo/neg) B cells in common variable immunodeficiency (CVID) patients with autoimmune cytopenia. Immunobiology 206 (2002) 502-513
25. Ko J., Radigan L., and Cunningham-Rundles C. Immune competence and switched memory B cells in common variable immunodeficiency. Clin Immunol 116 (2005) 37-41
26. Piqueras B., Lavenu-Bombled C., Galicier L., Bergeron-van der Cruyssen F., Mouthon L., Chevret S., et al. Common variable immunodeficiency patient classification based on impaired B cell memory differentiation correlates with clinical aspects. J Clin Immunol 23 (2003) 385-400
27. Kralovicova J., Hammarstrom L., Plebani A., Webster A.D., and Vorechovsky I. Fine-scale mapping at IGAD1 and genome-wide genetic linkage analysis implicate HLA-DQ/DR as a major susceptibility locus in selective IgA deficiency and common variable immunodeficiency. J Immunol 170 (2003) 2765-2775
28. Salzer U., Maul-Pavicic A., Cunningham-Rundles C., Urschel S., Belohradsky B.H., Litzman J., et al. ICOS deficiency in patients with common variable immunodeficiency. Clin Immunol 113 (2004) 234-240
29. Mullighan C.G., Fanning G.C., Chapel H.M., and Welsh K.I. TNF and lymphotoxin-alpha polymorphisms associated with common variable immunodeficiency: role in the pathogenesis of granulomatous disease. J Immunol 159 (1997) 6236-6241
30. Mullighan C.G., Marshall S.E., and Welsh K.I. Mannose binding lectin polymorphisms are associated with early age of disease onset and autoimmunity in common variable immunodeficiency. Scand J Immunol 51 (2000) 111-122
31. Carbone J., Escudero A., Mayayo M., Ballesteros M., Perez-Corral A., Sanchez-Ramon S., et al. Partial response to anti-CD20 monoclonal antibody treatment of severe immune thrombocytopenic purpura in a patient with common variable immunodeficiency. Ann N Y Acad Sci 1051 (2005) 666-671
32. Longhurst H.J., O'Grady C., Evans G., De Lord C., Hughes A., Cavenagh J., et al. Anti-D immunoglobulin treatment for thrombocytopenia associated with primary antibody deficiency. J Clin Pathol 55 (2002) 64-66
33. Saulsbury F.T., and Bringelsen K.A. Danazol therapy for chronic immune-mediated thrombocytopenic purpura in a patient with common variable immunodeficiency. Am J Pediatr Hematol Oncol 13 (1991) 326-329
34. Bonnet F., Morlat P., Viallard J.F., Pedeboscq S., DeWitte S., and Beylot J. Pulmonary granuloma, polyarthritis and antiphospholipids in common variable immunodeficiency: resolution after IVIG and the role of immunoglobulin A. Clin Exp Rheumatol 23 (2005) 428-429
35. Giannouli S., Anagnostou D., Soliotis F., and Voulgarelis M. Autoimmune manifestations in common variable immunodeficiency. Clin Rheumatol 23 (2004) 449-452
36. Smith K.J., and Skelton H. Common variable immunodeficiency treated with a recombinant human IgG, tumour necrosis factor-alpha receptor fusion protein. Br J Dermatol 144 (2001) 597-600
37. Liblau R.S., and Bach J.F. Selective IgA deficiency and autoimmunity. Int Arch Allergy Immunol 99 (1992) 16-27