Common variable immunodeficiency: Recent findings in cellular abnormalities;Inmunodeficiencia común variable: Hallazgos recientes sobre anormalidades celulares

Acta Bioquimica Clinica Latinoamericana

Volumn 38, Issue 4, 2004, Pages 489-494

  Serra, Horacio Marcelo ^a   Barcelona, Pablo Federico ^a   Collino, César Juan Gerardo ^a   Vettorazzi, Lorena ^b  

^a UNIVERSIDAD NACIONAL DE CÓRDOBA   (Argentina)

^b HOSPITAL PRIVADO   (Argentina)

Author keywords

Acquired immunity; Common variable immunodeficiency; Infection

Indexed keywords

IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; POLYSACCHARIDE;

ANTIGEN SPECIFICITY; B LYMPHOCYTE; CELL DAMAGE; CELL HETEROGENEITY; COMMON VARIABLE IMMUNODEFICIENCY; CORRELATION ANALYSIS; DIAGNOSTIC TEST; FOLLOW UP; HUMAN; HUMORAL IMMUNITY; HYPOGAMMAGLOBULINEMIA; IMMUNE RESPONSE; PATHOGENESIS; RESPIRATORY SYSTEM; REVIEW; T LYMPHOCYTE;

BACTERIA (MICROORGANISMS);

EID: 18844416364     PISSN: 03252957     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (45)

1. Ballow M. Primary immunodeficiency disorders: Antidody deficiency. J Allergy Clin Immunol 2001; 109: 581-91.
2. Cunningham-Rundles C, Bodian C. Common variable immunodeficiency: clinical and immunological features of 248 patients. Clin Immunol 1999; 92: 34-48.
3. Fasano M, Sullivan K, Sarpong S, Wood R, Lones S, Johns C, et al. Sarcoidiosis and common variable immunodeficiency. Report of 8 cases and review of the literature. Medicine 1996; 75: 251-61.
4. Report of a WHO Scientific Group. Primary Immunodeficiency Disease. Clinical and Experimental Immunology 1997; 109:1-28.
5. López Martín A, Hallal H, Barón JM, Vera F, Jiménez M, Conesa F. Alteraciones gastrointestinales en una paciente con inmunodeficiencia común variable. Gastroenterol Hepatol 2002; 25: 156-8.
6. Spicket, G. Current perspectives on common variable immunodeficiency (CVID). Clinical and Experimental Allergy 2001; 31: 536-42.
7. Aarli J. Immunoglobulins in epilepsy. Springer Semin Immunopathol 1985; 8: 5-28.
8. Zenone T, Souquet P, Cunningham-Rundles C, Bernard J. Hodgkin's disease associates with IgA and IgG subclass deficiency. J Intern Med 1996; 240 :99-102.
9. Hammarström L, Vorechovsky I, Webster D. Selective IgA deficiency (SigAD) and common variable immunodeficiency (CVID). Clin Exp Immunol 2000; 120: 225-31.
10. Vetrie D, Vorechovsky I, Sideras P, Holland J, Davies A, Flinter F, et al. The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases. Nature 1993; 361: 226-33.
11. Yel L, Minegishi Y, Coustan-Smith E, Buckley R, Trubel H, Pachman L, et al. Mutations in the mu heavy-chain gene in patients with agammaglobulinemia. N Engl J Med 1996; 335: 1523-5.
12. Notarangelo LD, Peitsch MC. CD40Ibase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome. Immunol Today 1996; 17: 511-6.
13. Serra HM, Baena-Cagnani CE, Mariant AL, Martin A, Garip EA, Pesoa SA. A new CD154 mutation. Allergy 2001; 56: 1230-1.
14. Llobet MP, Bertran JM, Español T. Inmunodeficiencia común variable en la edad pediátrica. Allergol et Immunopathol 2002; 30: 42-6.
15. Kinlen LJ, Webster AD, Bird AG, Haile R, Peto J, Soothill JF, et al. Propspective study of cancer in patients with hypogammaglobulinaemia. Lancet 1985; 1: 263-6.
16. Cunningham-Rundles C, Siegal FP, Cunningham-Rundles S, Lieberman P. Incidence of cancer in 98 patients with common varied immunodeficiency. J Clin Immunol 1987; 7: 294-6.
17. Mellemkjer L, Hammarström L, Andersen V, Yuen J, Heilmann C, Barington T, et al. Cancer risk among patients with IgA deficiency or common variable immunodeficiency and their relatives: a combined Danish and Swedish study. Clin Exp Immunol 2002; 130: 495-500.
18. Menso E, Romagnoli P, Criscuolo M, Barcelona P, Collino C, Serra H. Expresión de moléculas de adhesión leucocitarias en un paciente con IDCV. Alergia México 2004; 51: 13-22.
19. Rozynska KE, Spickett GP, Millrain M, Edwards A, Bryant A, Webster AD, et al. Accessory and T cell defects in acquired and inherited hypogammaglobulinaemia. Clin Exp Immunol 1989; 78: 1-6.
20. Pastorelli G, Roncarolo MG, Touraine JL, Peronne G, Tobo PA, de Vries JE. Peripheral blood lymphocytes of patients with common variable immunodeficiency (CVI) priduced reduced levels of interleukin-4, interleukin-2 and interferon-gamma, but proliferate normally uponactivation by mitogens. Clin Exp Immunol 1989; 78: 334-40.
21. Sneller MC, Strober W. Abnormalities of lymphokine gene expression in patients with common variable immunodeficiency. J Immunol 1990; 144: 3762-9.
22. Rump JA, Jahreis A, Shlesier M, Drager R, Melchers I, Peter HH. Possible role of IL-2 deficiency for hipogammaglobulinnaemia in patients with common variable immunodeficiency. Clin Exp Immunol 1992; 89: 204-10.
23. Fischer MB, Wolf HM, Hauber I, Eggenbauer H, Thon V, Sasgary M, et al. Activation via the antigen receptor is impaired in T cells, but not in B cells from patients with common variable immunodeficiency. Eur J Immunol 1996; 26: 231-7.
24. Thon V, Wolf HM, Sasgary M, Litzman J, Samstag A, Hauber I, et al. Defective integration of activating signals derived from the T cell receptor (TCR) and co-stimulatory molecules in both CD4+ and CD8+ T lymphocytes of common variable immunodeficiency (CVID) patients. Clin Exp Immunol 1997; 110: 174-81.
25. Majolini MB, D'Elios MM, Boncristiano M, Galieni P, Del Prete G, Telford JL, et al. Uncoupling of T-cell antigen receptor and downstream protein tyrosine kinases in common variable immunodeficiency. Clin Immunol Immunopathol 1997; 84: 98-102.
26. Boncristiano M, Majolini MB, D'Elios MM, Pacini S, Valensin S, Ulivieri C, et al. Defective recruitment and activation of ZAP-70 in common variable immunodeficiency patients with T cell defects. Eur J Immunol 2000; 30: 2632-8.
27. Fischer MB, Hauber I, Wolf HM, Vogel E, Mannhalter JW, Eibl MM. Impaired TCR signal traduction, but normal antigen presentation, in a patient with common variable immunodeficiency. Br J Haematol 1994; 88: 520-6.
28. Farrant J, Spickett G, Matamoros N, Copas D, Hernandez M, North M, et al. Study of B and T cell phenotypes in blood from patients with common variable immunodeficiency. Immunodeficiency 1994; 5: 159-69.
29. Spickett GP, Matamoros N, Farrant J. Lymphocyte phenotype in common variable immunodeficiency. Dis Markers 1992; 10: 67-80.
30. Farrington M, Grosmaire LS, Nonoyama S, Fischer SH, Hollenbaugh D, Ledbetter JA, et al. CD40 ligand expression is defective in a subset of patients with common variable immunodeficiency. Proc Natl Acad Sci USA 1994; 91: 1099-103.
31. Zhang JG, Morgan L, Spickett GP. L-selectin in patients with common variable immunodeficiency (CVID): a comparative study with normal individual. Clin Exp Immunol 1996; 104: 275-9.
32. Pozzi N, Gaetaniello L, Martire B, De Mattia D, Balestrieri B, Cosentini E, et al. Defective surface expression of atractin on T cells in patients with common variable immunodeficiency (CVID). Clin Exp Immunol 2001; 123: 99-104.
33. Spickett GP, Farrant J, North EN, Zhang J, Morgan L, Webster BD. Common variable immunodeficiency: how many diseases? Immunology Today 1997; 8: 325-8.
34. Bryant A, Calver NC, Toubi E, Webster AD, Farrant J. Classification of patients with common variable immunodeficiency by B cell secretion of IgM and IgG in response to anti-IgM and interleukin-2. Clin Immunol Immunopathol 1990; 56: 239-48.
35. Kruetzmann S, Rosado MM, Weber H, Germing U, Tournilhac O, Peter HH, et al. Human Immunoglobulin M memory B cells controlling Streptococcus pneumoniae infections are generated in the spleen. J Exp Med 2003; 197: 939-45.
36. Shinozaki K, Yasui K, Agematsu K. Direct B/B- cell interactions in immunoglobulin synthesis. Clin Exp Immunol 2001; 124: 386-91.
37. Jacquot S, Macon-Lemaitre L, Paris E, Kobata T, Tanaka Y, Morimoto C, et al. B cell co-receptors regulating T cell-dependent antibody production in common variable immunonodeficiency: CD27 pathway defects identify subsets of severely immuno-compromised patients. Int Immunol 2001; 13: 871-6.
38. -) in a subgroup of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease. Blood 2002; 99: 1544-51.
39. Groth C, Drager R, Warnatz K, Wolff-Vorbeck G, Schmidt S, Eibel H, et al. Impaired up-regulation of CD70 and CD86 in naive (CD27-) B cell from patients with common variable immunodeficiency. Clin Exp Immunol 2002; 129: 133-9.
40. Brouet JC, Chedeville A, Fermand JP, Royer B. Study of the B cell memory compartiment in common variable immunodeficiency. Eur J Immunol 2000; 30: 2516-20.
41. Endres R, Alimzhanov MB, Plitz T, Futterer A, Kosco-Vilbois MH, Nedospasov SA, et al. Mature folicular dendritic cell networks depend on expression of lymphotoxin β receptor by radioresistant stromal cells and of lymphotoxin and tumor necrosis factor by B cells. J Exp Med 1999; 189: 159-68.
42. Han S, Hathcock K, Zheng B, Kepler TB, Hodes R, Kelsoe G. Cellular interaction in germinal centers: role of CD40 ligand and B7-2 in established germinal centers. J Immunol 1995; 155: 556-67.
43. Ansel KM, Ngo VN, Hyman PL, Luther SA, Forster R, Sedgwick JD, et al. A chemokine-driven positive feedback loop organizas lymphoid follicles. Nature 2000; 406: 309-14.
44. Korthauer U, Graf D, Mages HW, Briere F, Padayachee M, Malcolm S, et al. Defective expression of T-cell CD40 ligand causes X-linked Immunodeficiency with hyper-IgM. Nature 1993; 361: 539-41.
45. DiSanto JP, Bonnefoy JY, Gauchat JF, Fischer A, de Saint BG. CD40 ligand mutations in x-linked Immunodeficiency with hyper-IgM. Nature 1993; 361: 541-3.