Common variable immunodeficiency and celiac disease;Déficit immunitaire commun variable et maladie cœliaque

Gastroenterologie Clinique et Biologique

Volumn 28, Issue 10 I, 2004, Pages 909-912

  Béchade, Dominique ^a   Desramé, Jérôme ^a   De Fuentés, Gilles ^a   Camparo, Philippe ^a   Raynaud, Jean Jacques ^a   Algayres, Jean Pierre ^a  

^a University of Paris Descartes   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CELIAC DISEASE; CHRONIC DISEASE; COMMON VARIABLE IMMUNODEFICIENCY; DIAGNOSTIC ERROR; DISEASE ASSOCIATION; GLUTEN FREE DIET; HUMAN; HUMAN TISSUE; INTESTINE VILLUS ATROPHY; MALABSORPTION; MALE; SENSITIVITY AND SPECIFICITY; SERODIAGNOSIS;

EID: 7044249047     PISSN: 03998320     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0399-8320(04)95157-3     Document Type: Article

References (19)

1. Sneller MC, Strober W, Eisenstein E, Jaffe JS, Cunningham-Rundles C. NIH Conference. New insights into common variable immunodeficiency. Ann Intern Med 1993;118:720-30.
2. Cunningham-Rundles C, Bodian C. Common variable immunodeficiency: clinical and immunological features of 248 patients. Clin Immunol 1999;92:34-48.
3. Bonhomme D, Hammarstrom L, Webster D, Chapel H, Hermine O, Le Deist F, et al. Impaired antibody affinity maturation process characterizes a subset of patients with common variable immunodeficiency. J Immunol 2000;165:4725-30.
4. Bloch-Michel C, Viallard JF, Blanco P, Liferman F, Neau D, Moreau JF, et al. Le déficit immunitaire commun variable de l'adulte: étude clinique, biologique et immunologique chez 17 malades. Rev Med Interne 2003;24:640-50.
5. Rosen FS, Cooper MD, Wedgwood RJ. The primary immunodeficiencies. N Engl J Med 1995;333:431-40.
6. Cunningham-Rundles C. Clinical and immunologic analyses of 103 patients with common variable immunodeficiency. J Clin Immunol 1989;9:22-33.
7. Bili H, Nizou C, Nizou JY, Coutant G, Schmoor P, Algayres JP, et al. Déficit immunitaire commun variable et atrophie villositaire totale régressive après régime sans gluten. Rev Med Interne 1997;18:724-6.
8. Sander CA, Medeiros LJ, Weiss LM, Yano T, Sneller MC, Jaffe ES. Lymphoproliferative lesions in patients with common variable immunodeficiency syndrome. Am J Surg Pathol 1992;16:1170-82.
9. Teahon K, Webster AD, Price AB, Weston J, Bjarnason I. Studies on the enteropathy associated with primary hypogammaglobulinaemia. Gut 1994;35:1244-9.
10. Farrell RJ, Kelly CP. Celiac sprue. N Engl J Med 2002;346:180-8.
11. Green PH, Jabri B. Coeliac disease. Lancet 2003;362:383-91.
12. Luzi G, Zullo A, Iebba F, Rinaldi V, Sanchez ML, Muscaritoli M, et al. Duodenal pathology and clinical-immunological implications in common variable immunodeficiency patients. Am J Gastroenterol 2003;98:118-21.
13. Webster AD, Slavin G, Shiner M, Platts-Mills TA, Asherson GL. Coeliac disease with severe hypogammaglobulinaemia. Gut 1981; 22:153-7.
14. Lopez Cruz MC, Martin Mateos MA, Giner Munoz MT, Plaza Martin AM, Sierra Martinez JI. Common variable immunodeficiency, insulin-dependent diabetes mellitus and celiac disease. Allergol Immunopathol (Madr) 2000;28:323-7.
15. Collin P, Maki M, Keyrilainen O, Hallstrom O, Reunala T, Pasternack A. Selective IgA deficiency and coeliac disease. Scand J Gastroenterol 1992;27:367-71.
16. Cataldo F, Marino V, Bottaro G, Greco P, Ventura A. Celiac disease and selective immunoglobulin A deficiency. J Pediatr 1997;131:306-8.
17. Cataldo F, Marino V, Ventura A, Bottaro G, Corazza GR. Prevalence and clinical features of selective immunoglobulin A deficiency in coeliac disease: an Italian multicentre study. Italian Society of Paediatric Gastroenterology and Hepatology (SIGEP) and "Club del Tenue" Working Groups on Coeliac Disease. Gut 1998;42:362-5.
18. Heneghan MA, Stevens FM, Cryan EM, Warner RH, McCarthy CF. Celiac sprue and immunodeficiency states: a 25-year review. J Clin Gastroenterol 1997;25:421-5.
19. Eijsbouts AM, Witteman BJ, de Sevaux RG, Fennis JF, van Haelst UJ, Naber AH, et al. Undefined malabsorption syndrome with villous atrophy successfully reversed by treatment with cyclosporine. Eur J Gastroenterol Hepatol 1995;7:803-6.